Physiological and metabolic control of diet selection
E. Roura A B and M. Navarro A
+ Author Affiliations
- Author Affiliations
A Centre for Nutrition and Food Sciences, Queensland Alliance for Agriculture and food Innovation, The University of Queensland, Qld 4072, Australia.
B Corresponding author. Email: e.roura@uq.edu.au
Animal Production Science 58(4) 613-626 https://doi.org/10.1071/AN16775
Submitted: 28 November 2016 Accepted: 11 October 2017 Published: 5 January 2018
Abstract
The fact that most farm animals have no dietary choice under commercial practices translates the dietary decisions to the carers. Thus, a lack of understanding of the principles of dietary choices is likely to result in a high toll for the feed industry. In healthy animals, diet selection and, ultimately, feed intake is the result of factoring together the preference for the feed available with the motivation to eat. Both are dynamic states and integrate transient stimulus derived from the nutritional status, environmental and social determinants of the animal with hard-wired genetic mechanisms. Peripheral senses are the primary inputs that determine feed preferences. Some of the sensory aspects of feed, such as taste, are innate and genetically driven, keeping the hedonic value of feed strictly associated with a nutritional frame. Sweet, umami and fat tastes are all highly appetitive. They stimulate reward responses from the brain and reinforce dietary choices related to essential nutrients. In contrast, aroma (smell) recognition is a plastic trait and preferences are driven mostly by learned experience. Maternal transfer through perinatal conditioning and the individual’s own innate behaviour to try or to avoid novel feed (often termed as neophobia) are known mechanisms where the learning process strongly affects preferences. In addtition, the motivation to eat responds to episodic events fluctuating in harmony with the eating patterns. These signals are driven mainly by gastrointestinal hormones (such as cholecystokinin [CCK] and glucagon-like peptide 1 [GLP-1]) and load. In addition, long-term events generate mechanisms for a sustainable nutritional homeostasis managed by tonic signals from tissue stores (i.e. leptin and insulin). Insulin and leptin are known to affect appetite by modulating peripheral sensory inputs. The study of chemosensory mechanisms related to the nutritional status of the animal offers novel tools to understand the dynamic states of feed choices so as to meet nutritional and hedonic needs. Finally, a significant body of literature exists regarding appetite driven by energy and amino acids in farm animals. However, it is surprising that there is scarcity of knowledge regarding what and how specific dietary nutrients may affect satiety. Thus, a better understanding on how bitter compounds and excess dietary nutrients (i.e. amino acids) play a role in no-choice animal feeding is an urgent topic to be addressed so that right choices can be made on the animal’s behalf.
Additional keywords: chemosensing, double-choice, perinatal conditioning, preferences, taste.
References
Adrian TE, Ferri GL, Bacare-Hamilton AJ, Fuessl HS, Polak JM, Bloom SR (1985) Human distribution and release of a putative new gut hormone, peptide YY. Gastroenterology 89, 1070–1077.| Human distribution and release of a putative new gut hormone, peptide YY.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL28XptFw%3D&md5=a25249bb89986e8076a169f5c0ab867bCAS |
Adrian TE, Bacarese-Hamilton AJ, Fuessl HS, Polak JM, Bloom SR (1987) Distribution and postprandial release of porcine peptide YY. The Journal of Endocrinology 113, 11–14.
| Distribution and postprandial release of porcine peptide YY.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2sXhsV2qtLk%3D&md5=3ea9e5b35618381a44a63c6673b8e584CAS |
Ahima RS, Antwi DA (2008) Brain regulation of appetite and satiety. Endocrinology and Metabolism Clinics of North America 37, 811–823.
| Brain regulation of appetite and satiety.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhsV2hu7k%3D&md5=d2fede473134d0ec8221edb7e180181bCAS |
Ajuwon KM, Kuske JL, Ragland D, Adeola O, Hancock DL, Anderson DB, Spurlock ME (2003) The regulation of IGF-1 by leptin in the pig is tissue specific and independent of changes in growth hormone. The Journal of Nutritional Biochemistry 14, 522–530.
| The regulation of IGF-1 by leptin in the pig is tissue specific and independent of changes in growth hormone.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXnsVanurY%3D&md5=d8ff472586d6c5b2f57e3148ce47df83CAS |
Alcantara PF, Hanson LE, Smith JD (1980) Sodium requirements, balance and tissue composition of growing pigs. Journal of Animal Science 50, 1092–1101.
| Sodium requirements, balance and tissue composition of growing pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXks12hsrk%3D&md5=2e5af80e64d1714ca0241432123e949bCAS |
Anderson R, Harvey R, Byrd J, Callaway T, Genovese K, Edrington T, Jung Y, McReynolds J, Nisbet D (2005) Novel preharvest strategies involving the use of experimental chlorate preparations and nitro-based compounds to prevent colonization of food-producing animals by foodborne pathogens. Poultry Science 84, 649–654.
| Novel preharvest strategies involving the use of experimental chlorate preparations and nitro-based compounds to prevent colonization of food-producing animals by foodborne pathogens.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXjtlaktrk%3D&md5=d562dd226dfb81d8cde025f7a548d402CAS |
Anika SM, Houpt TR, Houpt KA (1981) Cholecystokinin and satiety in pigs. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology 240, 310–318.
Arepally A, Barnett BP, Montgomery E, Patel TH (2007) Catheter-directed gastric artery chemical embolization for modulation of systemic ghrelin levels in a porcine model: initial experience. Radiology 244, 138–143.
| Catheter-directed gastric artery chemical embolization for modulation of systemic ghrelin levels in a porcine model: initial experience.Crossref | GoogleScholarGoogle Scholar |
Bachmanov AA, Beauchamp GK (2007) Taste receptor genes. Annual Review of Nutrition 27, 389–414.
| Taste receptor genes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhsVWisLvP&md5=55c3a24eae5c441dcd1efcf80d5db5d0CAS |
Baile CA, Della-Frare MA, Mclaughlin CL (1983) Hormones and feed intake. The Proceedings of the Nutrition Society 42, 113–127.
| Hormones and feed intake.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3sXlsFaisr0%3D&md5=0ffd94b3de5d1c8b52818cbb1106f665CAS |
Baldissera FGA, Holst JJ, Knuhtsen S, Hilsted L, Nielsen OL (1988) Oxyntomodulin (glicentin-(33–69): pharmacokinetics, binding to liver cell membranes, effects on isolated perfused pig pancreas, and secretion from isolated perfused lower small. Regulatory Peptides 21, 151–166.
| Oxyntomodulin (glicentin-(33–69): pharmacokinetics, binding to liver cell membranes, effects on isolated perfused pig pancreas, and secretion from isolated perfused lower small.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXktVWitb0%3D&md5=d831a78b146795272a760cbc13d82cfeCAS |
Baldwin BA (1980) Operant studies and preference tests on the role of olfaction and taste in the ingestive behaviour of pigs and ruminants. Advances in Animal Physiology and Animal Nutrition 11, 36–42.
Baldwin BA, De la Riva C (1992) Effect of food intake in pigs of antagonists acting on cholecystokinin type A and B receptors. The Journal of Physiology 446, 291
Baldwin BA, Cooper TR, Parrott RF (1983) Intravenous cholecystokinin octapeptide in pigs reduces operant responding for food, water, sucrose solution or radiant heat. Physiology & Behavior 30, 399–403.
| Intravenous cholecystokinin octapeptide in pigs reduces operant responding for food, water, sucrose solution or radiant heat.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3sXhvFansro%3D&md5=0b86a92f290890d2f46a229db445f690CAS |
Balleine BW, Dickinson A (1998) The role of incentive learning in instrumental outcome revaluation by sensory-specific satiety. Animal Learning & Behavior 26, 46–59.
| The role of incentive learning in instrumental outcome revaluation by sensory-specific satiety.Crossref | GoogleScholarGoogle Scholar |
Baranyiová E, Hullinger RL (1999) Effects of cholecystokinin on liquid diet intake of early-weaned piglets. Physiology & Behavior 68, 163–168.
Barb CR, Yan X, Azain MJ, Kraeling RR, Rampacek GB, Ramsay TG (1998) Recombinant porcine leptin reduces feed intake and stimulates growth hormone secretion in swine. Domestic Animal Endocrinology 15, 77–86.
| Recombinant porcine leptin reduces feed intake and stimulates growth hormone secretion in swine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXktlaquw%3D%3D&md5=c24afa3b4866a50f26e29d3fa52cf12cCAS |
Barb CR, Hausman GJ, Houseknecht KL (2001) Biology of leptin in the pig. Domestic Animal Endocrinology 21, 297–317.
| Biology of leptin in the pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XhsFWgu7k%3D&md5=479075b8795501bcc6758b6e95591a44CAS |
Barb CR, Kraeling RR, Rampacek GB, Hausman GJ (2006) The role of neuropeptide Y and interaction with leptin in regulating feed intake and luteinizing hormone and growth hormone secretion in the pig. Reproduction (Cambridge, England) 131, 1127–1135.
| The role of neuropeptide Y and interaction with leptin in regulating feed intake and luteinizing hormone and growth hormone secretion in the pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xpt1ehurc%3D&md5=48cae4a1295a9a42d2f6670e852a5e5eCAS |
Barbero A, Astiz S, Lopez-Bote CJ, Perez-Solana ML, Ayuso M, Garcia-Real I, Gonzalez-Bulnes A (2013) Maternal malnutrition and offspring sex determine juvenile obesity and metabolic disorders in a swine model of leptin resistance. PLoS One 8, e78424
| Maternal malnutrition and offspring sex determine juvenile obesity and metabolic disorders in a swine model of leptin resistance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhslWgsb3L&md5=75d3e5e37075c7a1ac0eb453caaa2df4CAS |
Barretero-Hernandez R, Galyean ML, Vizcarra JA (2010) The effect of feed restriction on plasma ghrelin, growth hormone, insulin, and glucose tolerance in pigs. The Professional Animal Scientist 26, 26–34.
| The effect of feed restriction on plasma ghrelin, growth hormone, insulin, and glucose tolerance in pigs.Crossref | GoogleScholarGoogle Scholar |
Bataille D, Tatemoto K, Gespach C, Jörnwall H, Rosselin G, Mutt V (1982) Isolation of glucagon-37 (bioactive enteroglicagon/oxyntomodulin) from porcine jejuno-ileum. FEBS Letters 146, 79–86.
| Isolation of glucagon-37 (bioactive enteroglicagon/oxyntomodulin) from porcine jejuno-ileum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL38XlslGlsr8%3D&md5=d254a8ecddf9d59f2006a479d30b08f0CAS |
Batterham RL, Cowley MA, Small CJ, Herzog H, Cohen MA, Dakin CL, Wren AM, Brynes AE, Low MJ, Ghatei MA, Cone RD, Bloom SR (2002) Gut hormone PYY (3–36) physiologically inhibits food intake. Nature 418, 650–654.
| Gut hormone PYY (3–36) physiologically inhibits food intake.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlvVylt7s%3D&md5=0f373a145172f86da7c846697f7955c6CAS |
Beauchamp GK, Menella JA (2009) Early flavor learning and its impact on later feeding behavior. Journal of Pediatric Gastroenterology and Nutrition 48, S25–30.
| Early flavor learning and its impact on later feeding behavior.Crossref | GoogleScholarGoogle Scholar |
Berridge KC, Kringelbach ML (2008) Affective neuroscience of pleasure: reward in humans and animals. Psychopharmacology 199, 457–480.
| Affective neuroscience of pleasure: reward in humans and animals.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXotVyrtrw%3D&md5=5216b4cf9b98e67d238f399c949f1945CAS |
Bishop AE, Polak JM, Bauer FE, Christofides ND, Carlei F, Bloo SR (1986) Occurrence and distribution of a newly discovered peptide, galanin, in the mammalian enteric nervous system. Gut 27, 849–857.
| Occurrence and distribution of a newly discovered peptide, galanin, in the mammalian enteric nervous system.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXhsVertLY%3D&md5=9db8b6c82ebcdecb05d5adfcb9270cd3CAS |
Black JL (1995) Approaches to modelling. In ‘Modelling growth in the pig’. (Eds PJ Moughan, MWA Verstegen, MI Visser-Reyneveld) pp. 11–22. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Black JL (2009) Models to predict feed intake. In ‘Voluntary feed intake in pigs’. (Eds D Torrallardona, E Roura) pp. 323–351. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Black JL (2014) Brief history and future of animal simulation models for science and application. Animal Production Science 54, 1883–1895.
| Brief history and future of animal simulation models for science and application.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhvVGgsLfO&md5=cbb0f13467a5ae07bf6f76b2e26b875dCAS |
Black JL, Kenney P (1984) Factors affecting diet selection by sheep. 2. Height and density of pasture. Australian Journal of Agricultural Research 35, 565–578.
| Factors affecting diet selection by sheep. 2. Height and density of pasture.Crossref | GoogleScholarGoogle Scholar |
Black JL, Williams BA, Gidley MJ (2009) Metabolic regulation of feed intake in monogastric mammals. In ‘Voluntary feed intake in pigs’. (Eds D Torrallardona, E Roura) pp. 189–213. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Black JL, Williams BA, Roura E, Gidley MJ (2011) Physiologic and metabolic regulation of feed intake. In ‘Manipulating pig production XIII: proceedings of the 13th biennial conference of the Australasian Pig Science Association’. (Ed. R van Barneveld) pp. 118–127. (Australasian Pig Science Association: Melbourne)
Blair R, FitzSimons J (1970) A note on the voluntary feed intake and growth of pigs given diets containing an extrimely bitter compound. Animal Production 12, 529–530.
| A note on the voluntary feed intake and growth of pigs given diets containing an extrimely bitter compound.Crossref | GoogleScholarGoogle Scholar |
Bolhuis JE, Oostindjer M, Van der Brand H, Gerrits WJJ, Kemp B (2009) Voluntary feed intake in piglets: potential impact of early experience with flavours derived from the maternal diet. In ‘Voluntary feed intake in pigs’. (Eds D Torrallardona, E Roura) pp. 37–52. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Bosi P, Mazzoni M, De Filippi S, Casini L, Trevisi P, Petrosino G, Lalatta-Costerbosa G (2006) A continuous dietary supply of free calcium formate negatively affects parietal cell population and gastric RNA expression for H+/K+-ATPase on weaning pigs. The Journal of Nutrition 136, 1229–1235.
Breer H, Eberle J, Frick C, Haid D, Widmayer P (2012) Gastrointestinal chemosensation: chemosensory cells in the alimentary tract. Histochemistry and Cell Biology 138, 13–24.
| Gastrointestinal chemosensation: chemosensory cells in the alimentary tract.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XosFSgsb0%3D&md5=97137c0bd918b68f9f7152072f0cb61dCAS |
Brown DR, Hildebrand KR, Parsons AM, Soldani G (1990) Effects of galanin on smooth muscle and mucosa of porcine jejunum. Peptides 11, 497–500.
| Effects of galanin on smooth muscle and mucosa of porcine jejunum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3cXktlGju7c%3D&md5=09e5dca30642eb4d9b3340f08746b46eCAS |
Camilleri M (2015) Peripheral mechanism in appetite regulation. Gastroenterology 148, 1219–1233.
| Peripheral mechanism in appetite regulation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXntVersLk%3D&md5=d6f2e50351ad5dd42bcfda2acfc31d43CAS |
Campbell RG (1976) A note on the use of a feed flavour to stimulate the feed intake of weaner pigs. Animal Science 23, 417–419.
Carroll JA, Allee GL (2009) Hormone control of feed intake in swine. In ‘Voluntary feed intake’. (Eds D Torrallardona, E Roura) pp. 155–187. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Chen HY, Trumbauer ME, Chen DT, Weingarth JR, Adams EG, Frazier EG, Shen Z, Marsh DJ, Feighner SD, Guan X-M, Ye Z, Nargund RP, Smith RG, Van Der Ploegh LHT, Howard AD, Macneil DJ, Qian S (2004) Orexigenic action of peripheral ghrelin is mediated by neuropetide Y and agouti-related protein. Endocrinology 145, 2607–2612.
| Orexigenic action of peripheral ghrelin is mediated by neuropetide Y and agouti-related protein.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXkt12gt7k%3D&md5=7e49be78056cd6e604296c22ce87fd07CAS |
Clouard C, Meunier-Salaün MC, Val-Laillet D (2012) Food preferences and aversions in human health and nutrition: how can pigs help the biomedical research? Animal 6, 118–136.
| Food preferences and aversions in human health and nutrition: how can pigs help the biomedical research?Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC38votlGmug%3D%3D&md5=23180a7d6fe2cef5377319fefbb9bf75CAS |
Clutter AC, Jiang R, McCann JP, Buchanan DS (1998) Plasma cholecystokinin-8 in pigs with divergent genetic potential for feed intake and growth. Domestic Animal Endocrinology 15, 9–21.
| Plasma cholecystokinin-8 in pigs with divergent genetic potential for feed intake and growth.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXktlSqtw%3D%3D&md5=016a59dad35eecf7ca26f1cfe4c3e538CAS |
Cohn C, Joseph D, Allweiss MD (1962) Nutritional effects of feeding frequency. The American Journal of Clinical Nutrition 11, 356–361.
Cortamira NO, Seve B, Lebreton Y, Ganier P (1991) Effect of dietary tryptophan on muscle, liver and whole-body protein synthesis in weaned piglets: relationship to plasma insulin. British Journal of Nutrition 66, 423–435.
| Effect of dietary tryptophan on muscle, liver and whole-body protein synthesis in weaned piglets: relationship to plasma insulin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK38XktVahtg%3D%3D&md5=4ea44687ae2c3fd5136e12e3a2ccb8e1CAS |
Cranwell PD (1995) Development of the neonatal gut and enzyme systems. In ‘The neonatal pig: development and survival’. (Ed. MA Varley) pp. 99–154. (CAB International: Wallingford, UK)
Cuber JC, Bernard C, Levenez F, Chayvialle JA (1990) Lipids, proteins and carbohydrates stimulate the secretion of intestinal cholecystokinin in the pig. Reproduction, Nutrition, Development 30, 267–275.
| Lipids, proteins and carbohydrates stimulate the secretion of intestinal cholecystokinin in the pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXkslShtL0%3D&md5=8fe94425c513122ab2700cb8cb2689b6CAS |
Cummings DE, Overduin J (2007) Gastrointestinal regulation of food intake. The Journal of Clinical Investigation 117, 13–23.
| Gastrointestinal regulation of food intake.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXmvV2rsg%3D%3D&md5=7e1dee83e5b4ad5cbd8c3b00e65fe28fCAS |
Cummings DE, Purnell JQ, Frayo R, Schmidova K, Wisse B, Weigle DA (2001) Prepandrial rise in plasma ghrelin levels suggest a role in meal initiation in humans. Diabetes 50, 1714–1719.
| Prepandrial rise in plasma ghrelin levels suggest a role in meal initiation in humans.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXlslKnurw%3D&md5=c01df33dc95c2c42cb403a83435bdd9fCAS |
Cutler R (2014) Managing pig health: a reference for the farm. Australian Veterinary Journal 92, 388
| Managing pig health: a reference for the farm.Crossref | GoogleScholarGoogle Scholar |
D’Alessio D (2008) Intestinal hormones and regulation of satiety: the case for CCK, GLP-1, PYY, and Apo A-IV. Journal of Parenteral and Enteral Nutrition 32, 567–568.
| Intestinal hormones and regulation of satiety: the case for CCK, GLP-1, PYY, and Apo A-IV.Crossref | GoogleScholarGoogle Scholar |
da Silva EC, de Jager N, Burgos-Paz W, Reverter A, Perez-Enciso M, Roura E (2014) Characterization of the porcine nutrient and taste receptor gene repertoire in domestic and wild populations across the globe. BMC Genomics 15, 1057
| Characterization of the porcine nutrient and taste receptor gene repertoire in domestic and wild populations across the globe.Crossref | GoogleScholarGoogle Scholar |
Dalby JA, Forbes JM, Varley MA, Jagger S (1995) The requirements of weaned piglets for a training period prior to a choice-feeding regime. Animal Science 61, 311–319.
| The requirements of weaned piglets for a training period prior to a choice-feeding regime.Crossref | GoogleScholarGoogle Scholar |
Dall’Aglio C, Zannoni A, Forni M, Bacci ML, Ceccarelli P, Boiti C (2013) Orexin system expression in the gastrointestinal tract of pigs. Research in Veterinary Science 95, 8–14.
| Orexin system expression in the gastrointestinal tract of pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXjtFGqsr4%3D&md5=003f8051dbd23a204c1d4b0431452105CAS |
Danilova V, Roberts T, Hellekant G (1999) Responses of single taste fibers and whole chorda tympani and glossopharyngeal nerve in the domestic pig, Sus scrofa. Chemical Senses 24, 301–316.
Delgado T (2013) Glutamate and GABA in appetite regulation. Frontiers in Endocrinology 4,
| Glutamate and GABA in appetite regulation.Crossref | GoogleScholarGoogle Scholar |
Dong XY, Xu J, Tang SQ, Li HY, Jiang QY, Zou XT (2009) Ghrelin and its biological effects on pigs. Peptides 30, 1203–1211.
| Ghrelin and its biological effects on pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmsVSgtLw%3D&md5=8cbeec2ecf4c11f35eeb3252fbf7b45dCAS |
Drazen DL, Vahl TP, D’Alessio DA, Seeley RJ, Woods SC (2006) Effects of a fixed meal pattern on ghrelin secretion pattern: evidence for a learned response independent of nutriotional status. Endocrinology 147, 23–30.
| Effects of a fixed meal pattern on ghrelin secretion pattern: evidence for a learned response independent of nutriotional status.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XptFWm&md5=369b1c61a64f83d8644777e0d7e21c10CAS |
Dryden G (2008) The nutritive value of concentrate foods. In ‘Animal nutrition science’. (Ed. G Dryden) pp. 57–73. (CAB International: Wallingford, UK)
Dunaiski V, Dunshea FR, Walton PE, Goddard C (1997) Long [R3] insulin-like growth factor-I reduces growth, plasma growth hormone, IGF binding protein-3 and endogenous IGF-I concentrations in pigs. The Journal of Endocrinology 155, 559–565.
| Long [R3] insulin-like growth factor-I reduces growth, plasma growth hormone, IGF binding protein-3 and endogenous IGF-I concentrations in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXnvVGgsbs%3D&md5=c858cbdef422f8023c82c9089f2cdaf2CAS |
Dunshea FR, Bittner EP, Pluske JR, Black JL (2017) Role of the gut, melanocortin system and malonyl-CoA in control of feed intake in non-ruminant animals. Animal Production Science
| Role of the gut, melanocortin system and malonyl-CoA in control of feed intake in non-ruminant animals.Crossref | GoogleScholarGoogle Scholar |
Dyer CJ, Touchette KJ, Carroll JA, Allee GL, Matteri RL (1999) Cloning of porcine prepro-orexin cdna and effects of an intramuscular injection of synthetic porcine orexin-b on feed intake in young pigs. Domestic Animal Endocrinology 16, 145–148.
| Cloning of porcine prepro-orexin cdna and effects of an intramuscular injection of synthetic porcine orexin-b on feed intake in young pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXjslClsrg%3D&md5=bcc6cd98185a33a08ecdf18dbbaddf23CAS |
Erlanson-Albertsson C (2011) The role of enterostatin in eating behavior and diet. In ‘Handbook of behavior, food and nutrition’. (Eds RV Preedy, RR Watson, RC Martin) pp. 217–240. (Springer: New York)
Erlanson-Albertsson C, Weström B, Pierzynowski S, Karlsson S (1991) Pancreatic procolipase activation peptide-enterostatin inhibits pancreatic enzyme secretion in the pig. Pancreas 6, 619–624.
| Pancreatic procolipase activation peptide-enterostatin inhibits pancreatic enzyme secretion in the pig.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK387ktFWkuw%3D%3D&md5=93e233d4a1c0124f35074b7147d63cb2CAS |
Ettle T, Roth FX (2004) Specific dietary selection for tryptophan by the piglet. Journal of Animal Science 82, 1115–1121.
| Specific dietary selection for tryptophan by the piglet.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXis1artr8%3D&md5=57c4d534c6a2a12960c581acbce99d99CAS |
Ettle T, Roth FX (2005) Dietary preferences for feeds varying in threonine concentration by the piglet. Physiology & Behavior 85, 289–295.
| Dietary preferences for feeds varying in threonine concentration by the piglet.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXlsFCqsb8%3D&md5=cb849cfabf3475124dafd435e18bc288CAS |
Ettle T, Roth FX (2009) Dietary selection for lysine by piglets at differing feeding regimen. Livestock Science 122, 259–263.
| Dietary selection for lysine by piglets at differing feeding regimen.Crossref | GoogleScholarGoogle Scholar |
Figueroa J, Solà-Oriol D, Manteca X, Pérez JF (2013a) Social learning of feeding behaviour in pigs: effects of neophobia and familiarity with the demonstrator conspecific. Applied Animal Behaviour Science 148, 120–127.
| Social learning of feeding behaviour in pigs: effects of neophobia and familiarity with the demonstrator conspecific.Crossref | GoogleScholarGoogle Scholar |
Figueroa J, Solà-Oriol D, Vinokurovas L, Manteca X, Pérez JF (2013b) Prenatal flavour exposure through maternal diets influences flavour preference in piglets before and after weaning. Animal Feed Science and Technology 183, 160–167.
| Prenatal flavour exposure through maternal diets influences flavour preference in piglets before and after weaning.Crossref | GoogleScholarGoogle Scholar |
Figueroa J, Solà-Oriol D, Manteca X, Pérez JF, Dwyer DM (2015) Anhedonia in pigs? Effects of social stress and restraint stress on sucrose preference. Physiology & Behavior 151, 509–515.
| Anhedonia in pigs? Effects of social stress and restraint stress on sucrose preference.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXhsVens7vF&md5=737196f33cf81980101e546d0dd0c6b7CAS |
Forbes JM (2007) Diet selection principles. In ‘Voluntary food intake and diet selection in farm animals’. (Ed. JM Forbes) pp. 144–171. (CAB International: Wallingford, UK)
Forbes JM, Provenza FD (2000) Integration of learning and metabolic signals into a theory of dietary choice and food intake. In ‘Ruminant physiology: digestion, metabolism, growth and reproduction’. (Ed. PB Cronje) pp. 3–19. (CAB International: Wallingford, UK)
Forbes JM, Shariatmadari F (1994) Diet selection for protein by poultry. World’s Poultry Science Journal 50, 7–24.
| Diet selection for protein by poultry.Crossref | GoogleScholarGoogle Scholar |
Friedman JM, Halaas L (1998) Leptin and the regulation of body weight in mammals. Nature 395, 763–770.
| Leptin and the regulation of body weight in mammals.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXmvFOmsL0%3D&md5=325360d7113feb3ea55ac00e54ae70caCAS |
Fulton S, Woodside B, Shizgal P (2000) Modulation of brain reward circuitry by leptin. Science 287, 125–128.
| Modulation of brain reward circuitry by leptin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXis1CisA%3D%3D&md5=d0492113c259de1952cabed2ded03d29CAS |
Furness JB (2016) Integrated neural and endocrine control of gastrointestinal function. In ‘ The enteric nervous system. Advances in experimental medicine and biology’. (Eds S Brierley, M Costa) pp. 159–173. (Springer International Publishing: Cham, Switzerland)
Glad H, Svendsen P, Ainsworth MA, Olsen O, Rehfeld JF, Schallalitzky de Muckadell OB (2009) The effect of gastrin-releasing peptide on porcine pancreaticobiliary bicarbonate secretion is mediated by secretin. Scandinavian Journal of Gastroenterology 29, 195–202.
Glaser D, Wanner M, Tinti JM, Nofre C (2000) Gustatory responses of pigs to various natural and artificial compounds known to be sweet in man. Food Chemistry 68, 375–385.
| Gustatory responses of pigs to various natural and artificial compounds known to be sweet in man.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXot1Gisg%3D%3D&md5=249b450805146619a9d5d546b7f5a211CAS |
Gloaguen M, Le Floc’h N, Corrent E, Primot Y, van Milgen J (2012) Providing a diet deficient in valine but with excess leucine results in a rapid decrease in feed intake and modifies the postprandial plasma amino acid and α-keto acid concentrations in pigs. American Society of Animal Science 90, 3135–3142.
Gloaguen M, Le Floc’h M, Corrent E, Primot Y, Val-Laillet D, Meunier-Salaün MC, van Milgen J (2013) Meal patterns in relation to the supply of branched-chain amino acids in pigs. Journal of Animal Science 91, 292–297.
| Meal patterns in relation to the supply of branched-chain amino acids in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXjsFKiu74%3D&md5=06d9c71166172ea64edf7b6a45a8a4a4CAS |
Gregory PC, McFadyen M, Rayner DV (1989a) Control of gastric emptying in the pig: influence of duodenal infusions of glucose and emulsified fat. Quarterly Journal of Experimental Physiology (Cambridge, England) 74, 109–119.
| Control of gastric emptying in the pig: influence of duodenal infusions of glucose and emulsified fat.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaL1M3msFGisA%3D%3D&md5=5431ff0790ffd3f5c58e4bbf066ff81bCAS |
Gregory PC, McFadyen M, Rayner DV (1989b) Relation between gastric emptying and short-term regulation of food intake in the pig. Physiology & Behavior 45, 677–683.
| Relation between gastric emptying and short-term regulation of food intake in the pig.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaL1Mzoslegtw%3D%3D&md5=eb47b0fe310378563a4782df83cd3003CAS |
Guzmán-Pino SA, Solà-Oriol D, Figueroa J, Borda E, Perez JF (2012) Dietary energy density affects the preference for protein or carbohydrate solutions and piglet performance after weaning. Journal of Animal Science 90, 71–73.
| Dietary energy density affects the preference for protein or carbohydrate solutions and piglet performance after weaning.Crossref | GoogleScholarGoogle Scholar |
Guzmán-Pino SA, Solà-Oriol D, Figueroa J, Pérez JF (2014) Influence of the protein status of piglets on their ability to select and prefer protein sources. Physiology & Behavior 129, 43–49.
| Influence of the protein status of piglets on their ability to select and prefer protein sources.Crossref | GoogleScholarGoogle Scholar |
Hansen L, Lampert S, Mineo H, Holst JJ (2004) Neural regulation of glucagon-like peptide-1 secretion in pigs. American Journal of Physiology. Endocrinology and Metabolism 287, E939–E947.
| Neural regulation of glucagon-like peptide-1 secretion in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtVaqs7vO&md5=9b6bce3533c2a9fee8d65150cf27284eCAS |
Havel PJ (2001) Peripheral signals conveying metabolic information to the brain: short-term and long-term regulation of food intake and energy homeostasis. Experimental Biology and Medicine 226, 963–977.
| Peripheral signals conveying metabolic information to the brain: short-term and long-term regulation of food intake and energy homeostasis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXptlOjsrs%3D&md5=fb9699bc4849e603002d055ca4f43b0cCAS |
Heflin LE, Makowsky R, Taylor JC, Williams MB, Lawrence AL, Watts SA (2016) Production and economic of dietary protein and carbohydrate in the culture of juvenile sea urchin Lytechinus variegatus. Aquaculture 463, 51–60.
Hetherington MM (1996) Sensory-specific satiety and its importance in meal termination. Neurosciences and Biobehavioral Reviews 20, 113–117.
Houpt TR (1984) Control of feeding in pigs. Journal of Animal Science 59, 1345–1353.
| Control of feeding in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2MXhslOitA%3D%3D&md5=2d66622d7768307b069b873989db80ecCAS |
Houseknecht KL, Baile CA, Matteri RL, Spurlock ME (1998) The biology of leptin: a review. Journal of Animal Science 76, 1405–1420.
| The biology of leptin: a review.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXjsVCjtbY%3D&md5=06b4bbaafd1b6bd56995d5548cf3e790CAS |
Ito T, ThidarMyint H, Murata T, Inoue H, Neyra RM, Kuwayama H (2006) Effects of peripheral administration of PYY3-36 on feed intake and plasma acyl-ghrelin levels in pigs. The Journal of Endocrinology 191, 113–119.
| Effects of peripheral administration of PYY3-36 on feed intake and plasma acyl-ghrelin levels in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xht1eju7nJ&md5=dcaa6651bafd3e39011104a9a73bf064CAS |
Jakob S, Mosenthin R, Sauer WC (2000) The influence of lipids on exocrine pancreatic secretion in pig: review. Asian-Australasian Journal of Animal Sciences 13, 711–719.
| The influence of lipids on exocrine pancreatic secretion in pig: review.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXisVCms7c%3D&md5=4783812f52126c37da54255a689beec9CAS |
Jenkins NL, Turner JL, Dritz SS, Durham SK, Minton JE (2004) Changes in circulating insulin-like growth factor-I, insulin-like growth factor binding proteins, and leptin in weaned pigs infected with Salmonella enterica serovar Typhimurium. Domestic Animal Endocrinology 26, 49–60.
| Changes in circulating insulin-like growth factor-I, insulin-like growth factor binding proteins, and leptin in weaned pigs infected with Salmonella enterica serovar Typhimurium.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXltFSgtg%3D%3D&md5=a0405f2ddd361bb20ac763f30ea2ea8bCAS |
Jensen AH, Terrill SW, Becker DE (1961) Response of the young pig to levels of dietary potassium. Journal of Animal Science 20, 464–467.
| Response of the young pig to levels of dietary potassium.Crossref | GoogleScholarGoogle Scholar |
Job RFS, Barnes BW (1995) Stress and consumption: inescapable shock, neophobia, and quinine finickiness in rats. Behavioral Neuroscience 109, 106–116.
| Stress and consumption: inescapable shock, neophobia, and quinine finickiness in rats.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK2M3ltFOrtQ%3D%3D&md5=df89acc5004b11be3aab685c86d02b75CAS |
Jobs EE, Enriori PJ, Cowley MA (2004) The electrophysiology of feeding circuits. Trends in Endocrinology and Metabolism 15, 448–499.
Kennedy JM, Baldwin BA (1972) Taste preferences in pigs for nutritive and non-nutritive sweet solutions. Animal Behaviour 20, 706–718.
| Taste preferences in pigs for nutritive and non-nutritive sweet solutions.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaE3s7otlSqtw%3D%3D&md5=6093adcc89b89c8893f10fa8590521d9CAS |
Kenney P, Black J (1984a) Factors affecting diet selection by sheep.1. Potential intake rate and acceptability of feed. Australian Journal of Agricultural Research 35, 551–563.
| Factors affecting diet selection by sheep.1. Potential intake rate and acceptability of feed.Crossref | GoogleScholarGoogle Scholar |
Kenney P, Black J (1984b) Factors affecting diet selection by sheep. 4. Level of feeding. Australian Journal of Agricultural Research 35, 839–843.
| Factors affecting diet selection by sheep. 4. Level of feeding.Crossref | GoogleScholarGoogle Scholar |
Kenney P, Black J, Colebrook W (1984) Factors affecting diet selection by sheep. 3. Dry matter content and particle length of forage. Australian Journal of Agricultural Research 35, 831–838.
| Factors affecting diet selection by sheep. 3. Dry matter content and particle length of forage.Crossref | GoogleScholarGoogle Scholar |
Kim JM, Ren D, Reverter A, Roura E (2016) A regulatory gene network related to the porcine umami taste receptor (TAS1R1/TAS1R3). Animal Genetics 47, 114–119.
| A regulatory gene network related to the porcine umami taste receptor (TAS1R1/TAS1R3).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28XhtFyrtrk%3D&md5=94f2c57f59219f5a03e4768e5fe59180CAS |
King RH, Pluske JR (2003) Nutritional management of the pig in preparation for weaning. In ‘Weaning the pig. Concepts and consequences’. (Eds JR Pluske, J Le Divinich, MWA Verstegen) pp. 37–52. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Knapper JME, Morgan LM, Fletcher JM, Marks V (1995a) Plasma and intestinal concentrations of GIP and GLP-1(7-36)amide during suckling and after weaning in pigs. Hormone and Metabolic Research. Hormon- und Stoffwechselforschung. Hormones et Metabolisme 27, 485–490.
| Plasma and intestinal concentrations of GIP and GLP-1(7-36)amide during suckling and after weaning in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XhvVKqug%3D%3D&md5=9336467f4b4afa905248de0969b2249fCAS |
Knapper JME, Health A, Fletcher JM, Morgan LM, Marks V (1995b) GIP and GLP-1(7-36)amide secretion in response to intraduodenal infusions in pigs. Comparative Biochemistry and Physiology 111, 445–450.
Kojima CJ, Carroll JA, Matteri RL, Touchette KJ, Allee GL (2007) Effects of weaning and weaning weight on neuroendocrine regulators of feed intake in pigs. Journal of Animal Science 85, 2133–2139.
| Effects of weaning and weaning weight on neuroendocrine regulators of feed intake in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXpsVGls74%3D&md5=8420884168074aa00e8f142a1c2dda3bCAS |
Konturek SJ, Konturek JW, Pawlik T, Brzozowski T (2004) Brain–gut axis ad its role in the control of food intake. Journal of Physiology and Pharmacology 55, 137–154.
Kringelbach ML, Stein A, van Hartevelt TJ (2012) The functional human neuroanatomy of food pleasure cycles. Physiology & Behavior 106, 307–316.
| The functional human neuroanatomy of food pleasure cycles.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XlvFymt7o%3D&md5=4083081f3ea741eb90b36c21fdda46c8CAS |
Kyriazakis I, Emmans GC, Whittemore CT (1990) Diet selection in pigs: choices made by growing pigs given foods of different protein concentrations. Animal Science 51, 189–199.
Kyriazakis I, Oldham JD, Coop RL, Jackson F (1994) The effect of subclinical intestinal nematode infection on the diet selection of growing sheep. British Journal of Nutrition 72, 665–677.
| The effect of subclinical intestinal nematode infection on the diet selection of growing sheep.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXis1enurY%3D&md5=a633006efe9eb5082e840c4ea7c5a409CAS |
Kyriazakis I, Anderson DH, Oldham JD, Coop RL, Jackson F (1996) Long-term subclinical infection with Trichostrongylus colubriformis: effects on food intake, diet selection and performance of growing lambs. Veterinary Parasitology 61, 297–313.
| Long-term subclinical infection with Trichostrongylus colubriformis: effects on food intake, diet selection and performance of growing lambs.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK28zltFylsg%3D%3D&md5=f2a0509297110240f888ce329d02fb2aCAS |
Langendijk P, Bolhuis JE, Laurenssen BFA (2007) Effects of pre- and postnatal exposure to garlic and aniseed flavour on pre- and postweaning feed intake in pigs. Livestock Science 108, 284–287.
| Effects of pre- and postnatal exposure to garlic and aniseed flavour on pre- and postweaning feed intake in pigs.Crossref | GoogleScholarGoogle Scholar |
Lapis TJ, Penner MH, Lim J (2016) Humans can taste glucose oligomers independent of the hT1R2/hT1R3 sweet taste receptor. Chemical Senses
| Humans can taste glucose oligomers independent of the hT1R2/hT1R3 sweet taste receptor.Crossref | GoogleScholarGoogle Scholar |
Lawrence AB, Terlouw EMC, Kiriazakis I (1993) The behavioural effects of undernutrition in confined farm animals. The Proceedings of the Nutrition Society 52, 219–229.
| The behavioural effects of undernutrition in confined farm animals.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3s3mt1Sgug%3D%3D&md5=cd22229ed45f00a13193d4064deba059CAS |
Le Dividich J, Seve B (2001) Energy requirement of the young pigs. In ‘The weaner pig’. (Eds MA Vaerley, J Wiseman) pp. 17–36. (CAB International: Wallingford, UK)
Le Quellec A, Kervran A, Blache P, Ciurana AJ, Bataille D (1992) Oxyntomodulin-like immunoreactivity: diurnal profile of a new potential enterogastrone. The Journal of Clinical Endocrinology and Metabolism 74, 1405–1409.
Lents CA, Barb CR, Hausman GJ, Nonneman D, Heidorm NL, Cisse RS, Azain MJ (2013) Effects of nesfatin-1 on food intake and LH secretion in prepubertal gilts and genomic association of the porcine NUCB2 gene with growth traits. Domestic Animal Endocrinology 45, 89–97.
| Effects of nesfatin-1 on food intake and LH secretion in prepubertal gilts and genomic association of the porcine NUCB2 gene with growth traits.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhtVKqsrvI&md5=dab054444c3cc0291deac69743c0958cCAS |
Li D, Zhang J (2014) Diet shapes the evolution of the vertebrate bitter taste receptor gene repertoire. Molecular Biology and Evolution 31, 303–309.
| Diet shapes the evolution of the vertebrate bitter taste receptor gene repertoire.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhtlalsLc%3D&md5=972226669722fbe3fe405a6f0319a889CAS |
Lin HC, Zhao XT, Wang L, Wong H (1996) Fat-induced ileal brake in the dog depends on peptide YY. Gastroenterology 110, 1491–1495.
| Fat-induced ileal brake in the dog depends on peptide YY.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XjtV2htLY%3D&md5=cc98839963bff02107da0b13f2963530CAS |
Lisonbee LD, Villalba JJ, Provenza FD, Hall JO (2009) Tannins and self-medication: implications for sustainable parasite control in herbivores. Behavioural Processes 82, 184–189.
| Tannins and self-medication: implications for sustainable parasite control in herbivores.Crossref | GoogleScholarGoogle Scholar |
Mahan DC (1982) Dietary calcium and phosphorus levels for weanling swine. Journal of Animal Science 54, 559–564.
| Dietary calcium and phosphorus levels for weanling swine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL38XhvFyhtrY%3D&md5=a9847cf09aa24530b3347f7aa4f34480CAS |
Maljaars PWJ, Peters HPF, Mela DJ, Masclee AAM (2008) Ileal brake: a sensible food target for appetite control. A review. Physiology & Behavior 95, 271–281.
| Ileal brake: a sensible food target for appetite control. A review.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtFOlsL%2FE&md5=ef658665b48ef2fcbdc44839b7e7ff6aCAS |
Mattson WJ (1980) Herbivory in relation to plant nitrogen content. Annual Review of Ecology Evolution and Systematics 11, 119–161.
| Herbivory in relation to plant nitrogen content.Crossref | GoogleScholarGoogle Scholar |
Mennella JA, Griffin CE, Beauchamp GK (2004) Flavor programming during infancy. Pediatrics 113, 840–845.
| Flavor programming during infancy.Crossref | GoogleScholarGoogle Scholar |
Moran AW, Al-Rammahi MA, Arora DK, Batchelo DJ, Coulter EA, Daly K, Ionescu C, Bravo D, Shirazi-Beechey SP (2010a) Expression of Na+/glucose co-transporter 1 (SGLT1) is enhanced by supplementation of the diet of weaning piglets with artificial sweeteners. British Journal of Nutrition 104, 637–646.
| Expression of Na+/glucose co-transporter 1 (SGLT1) is enhanced by supplementation of the diet of weaning piglets with artificial sweeteners.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtFCktbrE&md5=47aeb6c5f24ef1a957c3203b3875b344CAS |
Moran AW, Al-Rammahi MA, Arora DK, Batchelor DJ, Coulter EA, Daly K, Ionescu C, Bravo D, Shirazi-Beechey SP (2010b) Expression of Na+/glucose co-transporter 1 (SGLT1) in the intestine of piglets weaned to different concentrations of dietary carbohydrate. British Journal of Nutrition 104, 647–655.
| Expression of Na+/glucose co-transporter 1 (SGLT1) in the intestine of piglets weaned to different concentrations of dietary carbohydrate.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtFCktbzK&md5=ec1f3a342ae2f1408b155a9ecea996e2CAS |
Morrison CD, Xi I, White CL, Ye J, Martin RJ (2007) Amino acids inhibit Agrp gene expression via an mTOR-dependent mechanism. American Journal of Physiology. Endocrinology and Metabolism 293, E165–E171.
| Amino acids inhibit Agrp gene expression via an mTOR-dependent mechanism.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXosV2msb4%3D&md5=d155ce310b21354ee43b862cbce356b6CAS |
Munro PJ, Lirette A, Anderson DM, Ju HY (2000) Effects of a new sweetener, Stevia, on performance of newly weaned pigs. Canadian Journal of Animal Science 80, 529–531.
| Effects of a new sweetener, Stevia, on performance of newly weaned pigs.Crossref | GoogleScholarGoogle Scholar |
Newman RE, Downing JA, Thomson PC, Collins CL, Henman DJ, Wilkinson SJ (2014) Insulin secretion, body composition and pig performance are altered by feeding pattern. Animal Production Science 54, 319–328.
| Insulin secretion, body composition and pig performance are altered by feeding pattern.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXitVynsrg%3D&md5=2344a52f1a427c51c0371b80ffe9d10cCAS |
Oostindjer M, Bolhuis JE, van den Brand H, Roura E, Kemp B (2010) Prenatal flavor exposure affects growth, health and behavior of newly weaned piglets. Physiology & Behavior 99, 579–586.
| Prenatal flavor exposure affects growth, health and behavior of newly weaned piglets.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXjt1OhtL4%3D&md5=41ebdb3f2ae7d65cede143bc1064a8c5CAS |
Oostindjer M, Muñoz JM, Van den Brand H, Kemp B, Bolhuis JE (2011) Maternal presence and environmental enrichment affect food neophobia of piglets. Biology Letters 7, 19–22.
| Maternal presence and environmental enrichment affect food neophobia of piglets.Crossref | GoogleScholarGoogle Scholar |
Palou R, Fuller S, Smyth H, Roura E (2015) Transfer of dietary plant natural flavor compounds from essential oils to maternal fluids in pigs. Chemical Senses 40, 360
Parrott RF (1994) Central effects of CCK ligands in pigs making operant responses for food. Pharmacology, Biochemistry, and Behavior 49, 463–469.
| Central effects of CCK ligands in pigs making operant responses for food.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK2M7ms1ygtw%3D%3D&md5=ac999f0a564f212f7d2bdf2db7678aacCAS |
Pekas JC, Trout WE (1990) Stimulation of food intake and growth of swine by cholecystokinin immunization. Growth, Development, and Aging 54, 51–56.
Piórkowska K, Oczkowicz M, Różycki M, Ropka-Molik K, Kajtoch AP (2011) Novel porcine housekeeping genes for real-time RT-PCR experiments normalization in adipose tissue: assessment of leptin mRNA quantity in different pig breeds. Meat Science 87, 191–195.
| Novel porcine housekeeping genes for real-time RT-PCR experiments normalization in adipose tissue: assessment of leptin mRNA quantity in different pig breeds.Crossref | GoogleScholarGoogle Scholar |
Ramsay TG, Bush JA, McMurtry JP, Thivierge MC, Davis TA (2004) Peripheral leptin administration alters hormone and metabolite levels in the young pig. Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology 138, 17–25.
| Peripheral leptin administration alters hormone and metabolite levels in the young pig.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2c3mslOjsA%3D%3D&md5=4962eecc824cfb4eee1ebc06e413feccCAS |
Raubenheimer D, Simpson SJ (1993) The geometry of compensatory feeding in the locust. Animal Behaviour 45, 953–964.
| The geometry of compensatory feeding in the locust.Crossref | GoogleScholarGoogle Scholar |
Raubenheimer D, Simpson SJ (1997) Integrative models of nutrient balancing: aplication to insects and vertebrates. Nutrition Research Reviews 10, 151–179.
| Integrative models of nutrient balancing: aplication to insects and vertebrates.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXhvF2htQ%3D%3D&md5=b0c81beaddebb37850232650bafd80d7CAS |
Raubenheimer D, Simpson SJ (2004) Organismal stoichiometry: quantifying non-independence among food components. Ecology 85, 1203–1216.
| Organismal stoichiometry: quantifying non-independence among food components.Crossref | GoogleScholarGoogle Scholar |
Raubenheimer D, Simpson SJ, Mayntz D (2009) Nutrition, ecology and nutritional ecology: towards and integrated framework. Functional Ecology 23, 4–16.
| Nutrition, ecology and nutritional ecology: towards and integrated framework.Crossref | GoogleScholarGoogle Scholar |
Raun K, von Voss P, Knudsen LB (2007) Liraglutide, a once-daily human glucagon-like peptide-1 analog, minimizes food intake in severely obese minipigs. Obesity (Silver Spring, Md.) 15, 1710–1716.
| Liraglutide, a once-daily human glucagon-like peptide-1 analog, minimizes food intake in severely obese minipigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXptlGlt7c%3D&md5=56238c1c5325d249574f845101442a2aCAS |
Read NW, McFarlane A, Kinsman RI, Bates TE, Blackhall NW, Farrar GBJ, Hall JC, Moss G, Morris AP, O’Neill B, Welch I, Lee Y, Bloom SR (1984) Effect of infusion of nutrient solutions into the ileum on gastrointestinal transit and plasma levels of neurotensin and enteroglucagon. Gastroenterology 86, 274–280.
Reiners K, Hessel E, Van den Weghe H (2008) The effect of heademas on performance and feeding behavior of newly weaned piglets. Journal of Animal Science 86, 3600–3607.
| The effect of heademas on performance and feeding behavior of newly weaned piglets.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhsV2jsbvO&md5=2c5b858ab2d55e55cb893de3e40c3028CAS |
Reiter SS, Halsey CHC, Stronach BM, Bartosh JL, Owsley WF, Bergen WG (2007) Lipid metabolism related gene-expression profiling in liver, skeletal muscle and adipose tissue in crossbred Duroc and Pietrain pigs. Comparative Biochemistry and Physiology. Part D, Genomics & Proteomics 2, 200–206.
| Lipid metabolism related gene-expression profiling in liver, skeletal muscle and adipose tissue in crossbred Duroc and Pietrain pigs.Crossref | GoogleScholarGoogle Scholar |
Reynolds CB, Elias AN, Whisnant CS (2010) Effects of feeding pattern on ghrelin and insulin secretion in pigs. Domestic Animal Endocrinology 39, 90–96.
| Effects of feeding pattern on ghrelin and insulin secretion in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXosVGnsbc%3D&md5=0d9bad5ccae896b96844dedc8e35129fCAS |
Robbins CT, Fortin JK, Rode KD, Farley SD, Shipley LA, Felicetti LA (2007) Optimizing protein intake as a foraging strategy to maximize mass gain in an omnivore. Oikos 116, 1675–1682.
| Optimizing protein intake as a foraging strategy to maximize mass gain in an omnivore.Crossref | GoogleScholarGoogle Scholar |
Robert C, Palin M-F, Coulombe N, Roberge C (1998) Backfat thickness in pigs is positively associated with leptin mRNA levels. The Canadian Veterinary Journal. La Revue Veterinaire Canadienne 78, 473–482.
Rosero DS, Boyd RD, Odle J, van Heugten E (2016) Optimizing dietary lipid use to improve essential fatty acid status and reproductive performance of the modern lactating sow: a review. Journal of Animal Science and Biotechnology 7, 34
| Optimizing dietary lipid use to improve essential fatty acid status and reproductive performance of the modern lactating sow: a review.Crossref | GoogleScholarGoogle Scholar |
Roth FX, Meindl C, Ettle T (2006) Evidence of a dietary selection for methionine by the piglet. Veterinaria (México) 36, 11–24.
Rothman JM, Raubenheimer D, Chapman CA (2011) Nutritional geometry: gorillas prioritize non-protein energy while consuming surplus protein. Biology Letters 7, 847–849.
| Nutritional geometry: gorillas prioritize non-protein energy while consuming surplus protein.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xos1ajsQ%3D%3D&md5=5e5c85d8be3341fbeccdff4f32d7666dCAS |
Roura E (2011) Taste beyond taste. In ‘Manipulating pig production XIII: proceedings of the 13th biennial conference of the Australasian Pig Science Association’. (Ed. R van Barneveld.) pp. 106–117. (Australasian Pig Science Association: Melbourne)
Roura E, Tedo G (2009) Feed appetence in pigs: an oronasal sensing perspective. In ‘Voluntary feed intake in pigs’. (Eds D Torrallardona, E Roura) pp. 105–140. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Roura E, Risley C, Sola-Oriol D, Torrallardona D (2007) Responses to increasing doses of saccharin in piglet feeds on preference values and performance. Journal of Animal Science 85, 108
Roura E, Humphrey B, Tedó G, Ipharragerre I (2008) Unfolding the codes of short-term feed appetence in farm and companion animals. A comparative oronasal nutrient sensing biology review. Canadian Journal of Animal Science 88, 535–558.
| Unfolding the codes of short-term feed appetence in farm and companion animals. A comparative oronasal nutrient sensing biology review.Crossref | GoogleScholarGoogle Scholar |
Roura E, Humphrey B, Klasing KC, Swart M (2011) Is the pig a good umami sensing model for humans? A comparative taste receptor study. Flavour and Fragance Journal 26, 282–285.
Roura E, Baldwin MW, Klasing KC (2013) The avian taste system: potential implication in poultry nutrition. Animal Feed Science and Technology 180, 1–9.
| The avian taste system: potential implication in poultry nutrition.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhslGjsLfJ&md5=a840685be96c5d9032899765f0afbd6bCAS |
Roura E, Koopmans SJ, Lallès JP, Le Huerou-Luron I, de Jager N, Schuurman T, Val-Laillet D (2016) Critical review evaluating the pig as a model for numan nutritional physiology. Nutrition Research Reviews 13, 1–31.
Sahu A (1998) Evidence suggesting that galanin (GAL), melanin-concentrating hormone (MCH), neurotensin (NT), proopiomelanocortin (POMC) and neuropeptide Y (NPY) are targets of leptin signaling in the hypothalamus (1998). Endocrinology 139, 795–798.
| Evidence suggesting that galanin (GAL), melanin-concentrating hormone (MCH), neurotensin (NT), proopiomelanocortin (POMC) and neuropeptide Y (NPY) are targets of leptin signaling in the hypothalamus (1998).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXnslSjuw%3D%3D&md5=d8a1fd3bade8313636ab4c4a09d5bd02CAS |
Sahu A (2004) Minireview: a hypothalamic role in energy balance with special emphasis on leptin. Endocrinology 145, 2613–2620.
| Minireview: a hypothalamic role in energy balance with special emphasis on leptin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXkt12gt7Y%3D&md5=51864c03a247108b70871c6fb0a009cbCAS |
Sakurai T, Amemiya A, Ishii M, Matsuzaki I, Chemelli RM, Tanaka H, Williams SC, Richardson JA, Kozlowski GP, Wilson S, Arch JRS, Buckingham RE, Haynes AC, Carr SA, Annan RS, McNulty DE, Liu W-S, Terrett JA, Elshourbagy NA, Bergsma DJ, Yanagisawa M (1998) Orexins and orexin receptors: a family of hypothalamic neuropeptides and G-protein-coupled receptors that regulate feeding behavior. Cell 92, 573–585.
| Orexins and orexin receptors: a family of hypothalamic neuropeptides and G-protein-coupled receptors that regulate feeding behavior.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXhsVKntr4%3D&md5=21676379d14e38daac86a9faed62a31dCAS |
Salfen BE, Carroll JA, Keisler DH, Strauch TA (2004) Effects of exogenous ghrelin on feed intake, weight gain, behavior, and endocrine response in veanling pigs. Journal of Animal Science 82, 1957–1966.
| Effects of exogenous ghrelin on feed intake, weight gain, behavior, and endocrine response in veanling pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXlsFWksrk%3D&md5=fc093b45d3ed32d42d5ce5d9cbc73345CAS |
Satoh N, Ogawa Y, Katsuura G, Numata Y, Masuzaki H, Yoshimasa Y, Nakao K (1998) Satiety effect and sympathetic activation of leptin are mediated by hypotalamic melanocortin system. Neuroscience Letters 249, 107–110.
| Satiety effect and sympathetic activation of leptin are mediated by hypotalamic melanocortin system.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXjvVWisrY%3D&md5=81c0d9eda857b13cb64e443ecc4fb931CAS |
Sauleau P, Lapouble E, Val-Laillet D, Malbert CH (2009) The pig model in brain imaging and neurosurgery. Animal 3, 1138–1151.
| The pig model in brain imaging and neurosurgery.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC38vpt1Witg%3D%3D&md5=a445d3a0df29b32da090de29130e6e98CAS |
Sbarbati A, Merigo F, Benati D, Tizzano M, Bernardi P, Osculati F (2004) Laryngeal chemosensory clusters. Chemical Senses 29, 683–692.
| Laryngeal chemosensory clusters.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXotlWmsbY%3D&md5=ed32e4d90a801e48ad8fb612395b9a2fCAS |
Schmidt PT, Hansen L, Hilsted L, Holst JJ (2004) Cholecystokinin inhibits gastrin secretion independently of paracrine somatostatin secretion in the pig. Scandinavian Journal of Gastroenterology 39, 217–221.
| Cholecystokinin inhibits gastrin secretion independently of paracrine somatostatin secretion in the pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXjtFCntrc%3D&md5=c85c2bfa5f2b336125d523255a7074c7CAS |
Schoener TW (1971) Theory of feeding strategies. Annual Review of Ecology Evolution and Systematics 2, 369–404.
| Theory of feeding strategies.Crossref | GoogleScholarGoogle Scholar |
Schulze G, Watson NV (1995) Comments on ‘Flavor neophobia in selected rodent species’. In ‘Biological perpectives on motivated activities’. (Ed. R Wong) pp. 229–230. (Ablex Publishing Corporation: Norwood, NJ)
Scrimgeour K, Gresham MJ, Giles LR, Thomson PC, Wynn PC, Newman RE (2008) Ghrelin secretion is more closely aligned to energy balance than with feeding behaviour in the grower pig. The Journal of Endocrinology 198, 135–145.
| Ghrelin secretion is more closely aligned to energy balance than with feeding behaviour in the grower pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXpt12lsLk%3D&md5=fb0776efbac30c55556fa9852a8d3202CAS |
Shirazi-Beechey SP, Daly K, Al-Rammahi M, Moran AW, Bravo D (2014) Role of nutrient-sensing taste 1 receptor (T1R) family member in gastrointestinal chemosensing. British Journal of Nutrition 111, S8–S15.
| Role of nutrient-sensing taste 1 receptor (T1R) family member in gastrointestinal chemosensing.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXoslOku7c%3D&md5=8dc25e1d9fa4db0a53ed22197dc3e1bfCAS |
Simcock DC, Scott I, Przemeck SMC, Simpson HV (2006) Abomasal contents of parasitised sheep contain an inhibitor of gastrin secretion in vitro. Research in Veterinary Science 81, 225–230.
| Abomasal contents of parasitised sheep contain an inhibitor of gastrin secretion in vitro.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XlvF2rsrc%3D&md5=3b3e15a40b459867c947d20c83bf1f2dCAS |
Simpson SJ, Raubenheimer D (1993) A multi-level analysis of feeding behaviour: the geometry of nutritional decisions. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 342, 381–402.
| A multi-level analysis of feeding behaviour: the geometry of nutritional decisions.Crossref | GoogleScholarGoogle Scholar |
Simpson SJ, Raubenheimer D (2012) ‘The nature of nutrition. a unifying framework from animal adaptation to human obesity.’ (Princeton University Press: Princeton, NJ)
Simpson SJ, Sword GA, Lorch PD, Couzin ID (2006) Cannibal crickets on a forced march for protein and salt. Proceedings of the National Academy of Sciences, USA 103, 4152–4156.
| Cannibal crickets on a forced march for protein and salt.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XivFWiurY%3D&md5=2d7040fe9095b7e57e5ba577eb12c596CAS |
Solà-Oriol D, Roura E, Torrallardona D (2007a) Storage affects the palatability of protein sources in piglet diets. Journal of Animal Science 85, 77
Solà-Oriol D, Roura E, Torrallardona D (2007b) Interaction between the palatabilities of cereal and protein source in diets for pigs. Journal of Animal Science 85, 108–109.
Solà-Oriol D, Roura E, Torrallardona D (2009a) Feed preference in pigs: effect of cereal sources at different inclusion rates. Journal of Animal Science 87, 562–570.
| Feed preference in pigs: effect of cereal sources at different inclusion rates.Crossref | GoogleScholarGoogle Scholar |
Solà-Oriol D, Roura E, Torrallardona D (2009b) Feed preference in pigs: relationship with feed particle size and texture. Journal of Animal Science 87, 571–582.
| Feed preference in pigs: relationship with feed particle size and texture.Crossref | GoogleScholarGoogle Scholar |
Solà-Oriol D, Roura E, Torrallardona D (2009c) Use of double-choice feeding to quantify feed ingredient preferences in pigs. Livestock Science 123, 129–137.
| Use of double-choice feeding to quantify feed ingredient preferences in pigs.Crossref | GoogleScholarGoogle Scholar |
Solà-Oriol D, Roura E, Torrallardona D (2011) Feed preference in pigs: effect of selected protein, fat, and fiber sources at different inclusion rates. Journal of Animal Science 89, 3219–3227.
| Feed preference in pigs: effect of selected protein, fat, and fiber sources at different inclusion rates.Crossref | GoogleScholarGoogle Scholar |
Solà-Oriol D, Roura E, Torrallardona D (2014) Feed preference in pigs: relationship between cereal preference and nutrient composition and digestibility and digesta flow. Journal of Animal Science 92, 220–228.
| Feed preference in pigs: relationship between cereal preference and nutrient composition and digestibility and digesta flow.Crossref | GoogleScholarGoogle Scholar |
Solon-Biet SM, Walters KA, Simanainen UK, McMahon AC, Ruohonen K, Ballard JWO, Raubenheimer D, Handelsman DJ, Couteur DGL, Simpson SJ (2015) Macronutrient balance, reproductive function, and lifespan in aging mice. Proceedings of the National Academy of Sciences, USA 112, 3481–3486.
| Macronutrient balance, reproductive function, and lifespan in aging mice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXjs1Gru74%3D&md5=61a84f9ec86671aa1b5586718694d25dCAS |
Sørensen LB, Moller P, Flint A, Martens M, Raben A (2003) Effect of sensory perception of foods on appetite and food intake: a review of studies on humans. International Journal of Obesity 27, 1152–1166.
| Effect of sensory perception of foods on appetite and food intake: a review of studies on humans.Crossref | GoogleScholarGoogle Scholar |
Spiller RC, Trotman IF, Higgins BE, Ghatei MA, Grimble GK, Lee YC, Bloom SR, Misiewicz JJ, Silk DB (1984) The ileal brake-inhibition of jejunal motility after ileal fat perfusion in man. Gut 25, 365–374.
| The ileal brake-inhibition of jejunal motility after ileal fat perfusion in man.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2cXitVOgu78%3D&md5=7c387c3740c0e42f5713be491d218a5dCAS |
Spreckley E, Murphy KG (2015) The L-cell in nutritional sensing and the regulation of appetite. Frontiers in Nutrition 2, 23
| The L-cell in nutritional sensing and the regulation of appetite.Crossref | GoogleScholarGoogle Scholar |
Sterk A, Schlegel P, Mul A, Ubbink-Blanksma M, Bruininx E (2008) Effects of sweeteners on individual feed intake characteristics and performance in group-housed weanling pigs. Journal of Animal Science 86, 2990–2997.
| Effects of sweeteners on individual feed intake characteristics and performance in group-housed weanling pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtlCnsb%2FN&md5=a314f723434180e0ca209539b1b3c49fCAS |
Sternini C, Anselmi L, Rozengurt E (2008) Enteroendocrine cells: a site of ‘taste’ in gastrointestinal chemosensing. Current Opinion in Endocrinology, Diabetes, and Obesity 15, 73–78.
| Enteroendocrine cells: a site of ‘taste’ in gastrointestinal chemosensing.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXitFKgs74%3D&md5=cfdedc9ebcbdf7f587b7057c910a7572CAS |
Stockhorst U, De Fries D, Steingrueber H-J, Scherbaum WA (2004) Insulin and the CNS: effects on food intake, memory, and endocrine parameters and th erole of inanasal insulin administration in humans. Physiology & Behavior 83, 47–54.
| Insulin and the CNS: effects on food intake, memory, and endocrine parameters and th erole of inanasal insulin administration in humans.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXovV2gtLs%3D&md5=4162b878dc351bdac5cd193e6bd2b2e5CAS |
Suarez J, Roura E, Ipharraguerre I, Torrallardona D (2011a) Preference for diets with free L-tryptophan in pigs with different tryptophan status. Journal of Animal Science 89, 330
Suarez J, Roura E, Torrallardona D (2011b) Preference for diets with free DL-Met in pigs with different Met status. In ‘62nd annual meeting of the European Association for Animal Production’. (Ed. EAAP) p. 355. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Suarez J, Tedo G, Roura E, Torrallardona D (2011c) Weaned piglets prefer diets with L-lysine–HCL independent of their lysine nutritional status. Journées de la Recherche Porcine 43, 129–130.
Sugino T, Yamaura J, Yamagishi M, Ogura A, Hayashi R, Kurose Y, Kojima M, Kangamwa K, Hasegawa Y, Terashima Y (2002) A transient surge of ghrelin secretion before feeding is modified by different feeding regimens in sheep. Biochemical and Biophysical Research Communications 298, 785–788.
| A transient surge of ghrelin secretion before feeding is modified by different feeding regimens in sheep.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xot12kt7c%3D&md5=42c39c00f140abbba10e9a13ad7ab3b6CAS |
Tanaka K, Takizawa T, Oki O, Fukawa K, Ito T, Miyabe M, Mannen H, Kurosawa Y, Hirose K (2015) Allele frequency for c.335 A>C polymorphisms in porcine ghrelin/obestatin prepropeptide gene and assoication analysis with performance traits in various pig breeds. Czech Journal of Animal Science 60, 411–416.
| Allele frequency for c.335 A>C polymorphisms in porcine ghrelin/obestatin prepropeptide gene and assoication analysis with performance traits in various pig breeds.Crossref | GoogleScholarGoogle Scholar |
Tedo G, Roura E, Reina M, Ruiz-de la Torre JL, Mantexa X (2010) Well-fed piglets prefer amino acids that elicit umami taste. Journal of Animal Science 88, 211
Tempel DL, Leibowitz KJ, Leibowitz SF (1988) Effects of PVN galanin on macronutrient selection. Peptides 9, 309–314.
| Effects of PVN galanin on macronutrient selection.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXitFKlt7g%3D&md5=789e70cb4b29b4d16cd1ec1646f114b3CAS |
Tinti JM, Glaser D, Wanner M, Nofre C (2000) Comparison of gustatory responses to amino acids in pigs and in humans. Lebensmittel-Wissenschaft + Technologie 33, 578–583.
| Comparison of gustatory responses to amino acids in pigs and in humans.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXhsVGrs78%3D&md5=8051ab4dfe1d428a2f672ed42fc46409CAS |
Tomasetto C, Karam SM, Ribieras S, Masson R, Lefebvre O, Staub A, Alexander G, Chenard MP, Rio MC (2000) Identification and characterization of a novel gastric peptide hormone: the motilin-related peptide. Gastroenterology 119, 395–405.
| Identification and characterization of a novel gastric peptide hormone: the motilin-related peptide.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXmtVWrurw%3D&md5=4eab675078e98a5d351998285cc2c5e0CAS |
Tordoff MG (2002) Obesity by choice: the poweful influence of nutrient availability on nutrient intake. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology 282, R1536–R1539.
| Obesity by choice: the poweful influence of nutrient availability on nutrient intake.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XjslWlsrg%3D&md5=6013fdb936a4a4ef1320ad212a467ab0CAS |
Tordoff MG, Alarcón LK, Valmeki S, Jiang P (2012) T1R3: a human calcium taste receptor. Scientific Reports 2, 496
| T1R3: a human calcium taste receptor.Crossref | GoogleScholarGoogle Scholar |
Torrallardona D, Solà-Oriol D (2009) Evaluation of free-choice feedstuffs preference by pigs. In ‘Voluntary feed intake in pigs’. (Eds D Torrallardona, E Roura) pp. 215–242. (Wageningen Academic Publishers: Wageningen, The Netherlands)
Varricchio E, Russolillo MG, Russo F, Lombardi V, Paolucci M, Maruccio L (2014) Expression and immunohistochemical detection of nesfatin-1 in the gastrointestinal tract of Casertana pig. Acta Histochemica 116, 583–587.
| Expression and immunohistochemical detection of nesfatin-1 in the gastrointestinal tract of Casertana pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXitVShsbfP&md5=de96eb2c23241aacbdb8f03dca8a532aCAS |
Villalba JJ, Landau SY (2012) Host behavior, environment and ability to self-medicate. Small Ruminant Research 103, 50–59.
| Host behavior, environment and ability to self-medicate.Crossref | GoogleScholarGoogle Scholar |
Villalba JJ, Provenza FD (2007) Self-medication and homeostatic behaviour in herbivores: learning about the benefits of nature’s pharmacy. Animal 1, 1360–1370.
| Self-medication and homeostatic behaviour in herbivores: learning about the benefits of nature’s pharmacy.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC38vpt1WlsA%3D%3D&md5=75fae5726d90cdff13d55d72d7779f0bCAS |
Villalba JJ, Provenza FD (2009) Learning and dietary choice in herbivores. Rangeland Ecology and Management 62, 399–406.
| Learning and dietary choice in herbivores.Crossref | GoogleScholarGoogle Scholar |
Villalba JJ, Provenza FD, Shaw R (2006) Sheep self-medicate when challenged with illness-inducing foods. Animal Behaviour 71, 1131–1139.
| Sheep self-medicate when challenged with illness-inducing foods.Crossref | GoogleScholarGoogle Scholar |
Villalba JJ, Miller J, Hall JO, Clemensen AK, Stott R, Snyder D, Provenza FD (2013) Preference for tanniferous (Onobrychis viciifolia) and non-tanniferous (Astragalus cicer) forage plants by sheep in response to challenge infection with Haemonchus contortus. Small Ruminant Research 112, 199–207.
| Preference for tanniferous (Onobrychis viciifolia) and non-tanniferous (Astragalus cicer) forage plants by sheep in response to challenge infection with Haemonchus contortus.Crossref | GoogleScholarGoogle Scholar |
Wellendorph P, Johansen LD, Bräuner-Osborne H (2010) The emerging role of promiscous 7TM receptors as chemosensors for food intake. Vitamins and Hormones 84, 151–184.
| The emerging role of promiscous 7TM receptors as chemosensors for food intake.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXotlOktw%3D%3D&md5=6b71ced0c6abfc29197dbcd4d9fd6b23CAS |
Wen J, Phillips SF, Sarr MG, Kost LJ, Holst JJ (1995) PYY and GLP-1 contribute to feedback inhibition from the canine ileum and colon. The American Journal of Physiology 269, 945–952.
White TCR (1993) ‘The inadequate environment: nitrogen and the abundance of animals.’ (Springer Verlag: Berlin)
Whitley NC, Barb CR, Kraeling RR, Barrett JB, Rampacek GB, Carroll JA, Keisler DH (2000) Feed intake and serum GH, LH and cortisol in gilts after intracerebroventricular or intravenous injection of urocortin. Domestic Animal Endocrinology 19, 209–221.
| Feed intake and serum GH, LH and cortisol in gilts after intracerebroventricular or intravenous injection of urocortin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXoslGhur0%3D&md5=cd05415fd7ff2e4860650918ca5f8367CAS |
Wierup N, Björkqvist M, Weström B, Pierzynowski S, Sundler F, Sjölund K (2007) Ghrelin and motilin are co-secreted from a prominent endocrine cell population in the small intestine. The Journal of Clinical Endocrinology and Metabolism 92, 3573–3581.
| Ghrelin and motilin are co-secreted from a prominent endocrine cell population in the small intestine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVGqsrbP&md5=0512ba61661dc1bad6d0cf27169f0dd4CAS |
Woods SC, Lutz TA, Geary N, Langhans W (2006) Pancreatic signals controlling food intake; insulin, glucagon and amylin. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 361, 1219–1235.
| Pancreatic signals controlling food intake; insulin, glucagon and amylin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtVygtL7I&md5=4dcd96603f0a38159da9c7631dffafbeCAS |
Yao Y, Lu S, Huang Y, Beeman-Black CC, Lu R, Pan X, Hussain MM, Black DD (2011) Regulation of microsomal triglyceride transfer protein by apolipoprotein A-IV in newborn swine intestinal epithelial cells. American Journal of Physiology. Gastrointestinal and Liver Physiology 300, G357–G363.
| Regulation of microsomal triglyceride transfer protein by apolipoprotein A-IV in newborn swine intestinal epithelial cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXisFyis7c%3D&md5=245be1e15b3b1fe0e137ef5d8ffef068CAS |
Yearsley JM, Villalba J, Gordon IJ, Kyriazakis I, Speakman JR, Tolkamp BJ, Illius AW, Duncan AJ (2006) A theory of associating food types with their postingestive consequences. American Naturalist 167, 705–716.
| A theory of associating food types with their postingestive consequences.Crossref | GoogleScholarGoogle Scholar |
Yin J, Li X, Li D, Yue T, Fang Q, Ni J, Zhou X, Wu G (2009) Dietary supplementation with zinc oxide stimulates ghrelin secretion from the stomach of young pigs. The Journal of Nutritional Biochemistry 20, 783–790.
| Dietary supplementation with zinc oxide stimulates ghrelin secretion from the stomach of young pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtFanu7%2FI&md5=28932d529f5ace3c2d22c10f0e58b8d2CAS |
Zabielski R (2007) Hormonal and neural regulation of intestinal function in pigs. Livestock Science 108, 32–40.
| Hormonal and neural regulation of intestinal function in pigs.Crossref | GoogleScholarGoogle Scholar |
Zhang H, Yin J, Li D, Zhou X, Li X (2007a) Tryptophan enhances ghrelin expression and secretion associated with increased food intake and weight gain in weanling pigs. Domestic Animal Endocrinology 33, 47–61.
| Tryptophan enhances ghrelin expression and secretion associated with increased food intake and weight gain in weanling pigs.Crossref | GoogleScholarGoogle Scholar |
Zhang K, Yuan Z, Bing Y, Chen X, Ding X, Chen D (2007b) Effects of active immunization against cholecystokinin 8 on performance, contents of serum hormones, and expressions of CCK gene and CCK receptor gene in pigs. Endocrine 32, 338–344.
| Effects of active immunization against cholecystokinin 8 on performance, contents of serum hormones, and expressions of CCK gene and CCK receptor gene in pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXks1Glur4%3D&md5=4c757c6ed2c172160ee122f20645be4eCAS |
