A comparative study of brain activation patterns associated with sexual arousal between males and females using 3.0-T functional magnetic resonance imaging
Gwang-Won Kim A and Gwang-Woo Jeong A B CA Research Institute of Medical Imaging, Chonnam National University Medical School, Gwangju 501-757, Korea.
B Department of Radiology, Chonnam National University Medical School, Chonnam National University Hospital, Gwangju 501-757, Korea.
C Corresponding author. Email: gwjeong@jnu.ac.kr
Sexual Health 11(1) 11-16 https://doi.org/10.1071/SH13127
Submitted: 15 May 2013 Accepted: 1 October 2013 Published: 13 December 2013
Abstract
Background: In contrast to the previous studies using a 1.5-T magnetic resonance imaging system, our study was performed on a higher magnetic field strength, 3.0 T, to gain more valuable information on the functional brain anatomy associated with visual sexual arousal for discriminating the gender difference by increasing the detection power of brain activation. Methods: Twenty-four healthy subjects consisting of 12 males and 12 females underwent functional magnetic resonance imaging examination for this study. Brain activity was measured while viewing erotic videos. Results: The predominant activation areas observed in males as compared with females included the hypothalamus, the globus pallidus, the head of the caudate nucleus, the parahippocampal gyrus, the amygdala and the septal area, whereas the predominant activation in females was observed in the anterior cingulate gyrus and the putamen. Conclusion: Our findings suggest that the brain activation patterns associated with visual sexual arousal are specific to gender. This gender difference in brain activation patterns is more remarkable at higher magnet field (3.0 T) than at 1.5 T.
Additional keywords: gender difference, high field.
References
[1] Dulac C, Kimchi T. Neural mechanisms underlying sex-specific behaviors in vertebrates. Curr Opin Neurobiol 2007; 17 675–83.| Neural mechanisms underlying sex-specific behaviors in vertebrates.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXjs1Kmsrg%3D&md5=138e99e353798e3e2861244be5625075CAS | 18343651PubMed |
[2] Kelly SJ, Ostrowski NL, Wilson MA. Gender differences in brain and behavior: hormonal and neural bases. Pharmacol Biochem Behav 1999; 64 655–64.
| Gender differences in brain and behavior: hormonal and neural bases.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXnsVKksL0%3D&md5=8028cecd543ed32705fcdab54d0255ffCAS | 10593187PubMed |
[3] Baldwin JD, Baldwin JI. Gender differences in sexual interest. Arch Sex Behav 1997; 26 181–210.
| Gender differences in sexual interest.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK2s3lsFKrtA%3D%3D&md5=3759ce69bf6d58d886943001bd863f3eCAS | 9101033PubMed |
[4] Leon-Carrion J, Martin-Rodriguez JF, Damas-Lopez J, Pourrezai K, Izzetoglu K, Barroso Y, et al Does dorsolateral prefrontal cortex (DLPFC) activation return to baseline when sexual stimuli cease? The role of DLPFC in visual sexual stimulation. Neurosci Lett 2007; 416 55–60.
| Does dorsolateral prefrontal cortex (DLPFC) activation return to baseline when sexual stimuli cease? The role of DLPFC in visual sexual stimulation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXjsVeku7s%3D&md5=051b063741ec84853b5076771634c6f8CAS | 17316990PubMed |
[5] Rupp HA, Wallen K. Sex differences in viewing sexual stimuli: an eye-tracking study in men and women. Horm Behav 2007; 51 524–33.
| Sex differences in viewing sexual stimuli: an eye-tracking study in men and women.Crossref | GoogleScholarGoogle Scholar | 17362952PubMed |
[6] Canli T, Gabrieli JD. Imaging gender differences in sexual arousal. Nat Neurosci 2004; 7 325–6.
| Imaging gender differences in sexual arousal.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXisFCisrk%3D&md5=403704cfa40514f487af3e94a52992cfCAS | 15048119PubMed |
[7] Huettel SA, Son AW, Mccarthy G. Functional magnetic resonance imaging. Sunderland: Sinauer Associates; 2004.
[8] Beauregard M, Levesque J, Bourgouin P. Neural correlates of conscious self-regulation of emotion. J Neurosci 2001; 21 RC165
| 1:STN:280:DC%2BD3Mrgt1Ohuw%3D%3D&md5=36a66738f948d939e2207228395ed151CAS | 11549754PubMed |
[9] Park K, Kang HK, Seo JJ, Kim HJ, Ryu SB, Jeong GW. Blood-oxygenation-level-dependent functional magnetic resonance imaging for evaluating cerebral regions of female sexual arousal response. Urology 2001; 57 1189–94.
| Blood-oxygenation-level-dependent functional magnetic resonance imaging for evaluating cerebral regions of female sexual arousal response.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD387hslOrtA%3D%3D&md5=57099a50b00558fe0be903c7db4829f7CAS | 11377345PubMed |
[10] Jeong GW, Park K, Youn G, Kang HK, Kim HJ, Seo JJ, et al Assessment of cerebrocortical regions associated with sexual arousal in premenopausal and menopausal women by using BOLD-based functional MRI. J Sex Med 2005; 2 645–51.
| Assessment of cerebrocortical regions associated with sexual arousal in premenopausal and menopausal women by using BOLD-based functional MRI.Crossref | GoogleScholarGoogle Scholar | 16422822PubMed |
[11] Karama S, Lecours AR, Leroux JM, Bourgouin P, Beaudoin G, Joubert S, et al Areas of brain activation in males and females during viewing of erotic film excerpts. Hum Brain Mapp 2002; 16 1–13.
| Areas of brain activation in males and females during viewing of erotic film excerpts.Crossref | GoogleScholarGoogle Scholar | 11870922PubMed |
[12] Gizewski ER, Krause E, Karama S, Baars A, Senf W, Forsting M. There are differences in cerebral activation between females in distinct menstrual phases during viewing of erotic stimuli: a fMRI study. Exp Brain Res 2006; 174 101–8.
| There are differences in cerebral activation between females in distinct menstrual phases during viewing of erotic stimuli: a fMRI study.Crossref | GoogleScholarGoogle Scholar | 16604320PubMed |
[13] Hamann S, Herman RA, Nolan CL, Wallen K. Men and women differ in amygdala response to visual sexual stimuli. Nat Neurosci 2004; 7 411–6.
| Men and women differ in amygdala response to visual sexual stimuli.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXisFCis7k%3D&md5=d0960dfaf0f5dfb9afd488612024f34cCAS | 15004563PubMed |
[14] Yang JC, Park K, Eun SJ, Lee MS, Yoon JS, Shin IS, et al Assessment of cerebrocortical areas associated with sexual arousal in depressive women using functional MR imaging. J Sex Med 2008; 5 602–9.
| Assessment of cerebrocortical areas associated with sexual arousal in depressive women using functional MR imaging.Crossref | GoogleScholarGoogle Scholar | 18194182PubMed |
[15] Maldjian JA, Laurienti PJ, Kraft RA, Burdette JH. An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets. Neuroimage 2003; 19 1233–9.
| An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets.Crossref | GoogleScholarGoogle Scholar | 12880848PubMed |
[16] Krasnow B, Tamm L, Greicius MD, Yang TT, Glover GH, Reiss AL, et al Comparison of fMRI activation at 3 and 1.5 T during perceptual, cognitive, and affective processing. Neuroimage 2003; 18 813–26.
| Comparison of fMRI activation at 3 and 1.5 T during perceptual, cognitive, and affective processing.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3s3gs12ksQ%3D%3D&md5=a221084752b824d5581872cf6fdfbebfCAS | 12725758PubMed |
[17] Scarabino T, Giannatempo GM, Popolizio T, Tosetti M, d’Alesio V, Esposito F, et al 3.0-T functional brain imaging: a 5-year experience. Radiol Med (Torino) 2007; 112 97–112.
| 3.0-T functional brain imaging: a 5-year experience.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2s7lsVequg%3D%3D&md5=50aa7719fbcbf556cd318d6266c75da2CAS |
[18] Arnow BA, Desmond JE, Banner LL, Glover GH, Solomon A, Polan ML, et al Brain activation and sexual arousal in healthy, heterosexual males. Brain 2002; 125 1014–23.
| Brain activation and sexual arousal in healthy, heterosexual males.Crossref | GoogleScholarGoogle Scholar | 11960892PubMed |
[19] Sachs BD, Meisel RL. The physiology of male sexual behavior. In Knobil E, Neill JD, editors. Physiology of reproduction. New York: Raven Press; 1994.pp. 3–105
[20] Redouté J, Stoleru S, Gregoire MC, Costes N, Cinotti L, Lavenne F, et al Brain processing of visual sexual stimuli in human males. Hum Brain Mapp 2000; 11 162–77.
| Brain processing of visual sexual stimuli in human males.Crossref | GoogleScholarGoogle Scholar | 11098795PubMed |
[21] Gorman DG, Cummings JL. Hypersexuality following septal injury. Arch Neurol 1992; 49 308–10.
| Hypersexuality following septal injury.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK387mtF2ksg%3D%3D&md5=dedb50dce76466d9df1052909a55cd39CAS | 1536635PubMed |
[22] Stoléru S, Grégoire MC, Gérard D, Decety J, Lafarge E, Cinotti L, et al Neuroanatomical correlates of visually evoked sexual arousal in human males. Arch Sex Behav 1999; 28 1–21.
| Neuroanatomical correlates of visually evoked sexual arousal in human males.Crossref | GoogleScholarGoogle Scholar | 10097801PubMed |
[23] Giuliano F, Bernabe J, Brown K, Droupy S, Benoit G, Rampin O. Erectile response to hypothalamic stimulation in rats: role of peripheral nerves. Am J Physiol 1997; 273 R1990–7.
| 1:CAS:528:DyaK1cXjsVOhug%3D%3D&md5=9eec63fa0d1e173243eed67a981a2391CAS | 9435653PubMed |
[24] Stoleru SG, Ennaji A, Cournot A, Spira A. LH pulsatile secretion and testosterone blood levels are influenced by sexual arousal in human males. Psychoneuroendocrinology 1993; 18 205–18.
| LH pulsatile secretion and testosterone blood levels are influenced by sexual arousal in human males.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXksVWhtLs%3D&md5=36c53b51ad1800774d767fb2d942fa96CAS | 8516424PubMed |
[25] Temel Y, Hafizi S, Tan S, Visser-Vandewalle V. Role of the brain in the control of erection. Asian J Androl 2006; 8 259–64.
| Role of the brain in the control of erection.Crossref | GoogleScholarGoogle Scholar | 16625274PubMed |
[26] Baird AD, Wilson SJ, Bladin PF, Saling MM, Reutens DC. The amygdala and sexual drive: insights from temporal lobe epilepsy surgery. Ann Neurol 2004; 55 87–96.
| The amygdala and sexual drive: insights from temporal lobe epilepsy surgery.Crossref | GoogleScholarGoogle Scholar | 14705116PubMed |
[27] Cahill L, Haier RJ, White NS, Fallon J, Kilpatrick L, Lawrence C, et al Sex-related difference in amygdala activity during emotionally influenced memory storage. Neurobiol Learn Mem 2001; 75 1–9.
| Sex-related difference in amygdala activity during emotionally influenced memory storage.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3M7htFWkug%3D%3D&md5=e02340fb3ca3ed45a520c64d9c35d26bCAS | 11124043PubMed |
[28] Ponseti J, Bosinski HA, Wolff S, Peller M, Jansen O, Medhorn HM, et al A functional endophenotype for sexual orientation in humans. Neuroimage 2006; 33 825–33.
| A functional endophenotype for sexual orientation in humans.Crossref | GoogleScholarGoogle Scholar | 16979350PubMed |
[29] Reiman EM, Lane RD, Ahern GL, Schwartz GE, Davidson RJ, Friston KJ, et al Neuroanatomical correlates of externally and internally generated human emotion. Am J Psychiatry 1997; 154 918–25.
| 1:STN:280:DyaK2szlsVCluw%3D%3D&md5=82dd381a5edf7d7c27ff7174cc9fde13CAS | 9210741PubMed |
[30] Llinas R, Ribary U, Contreras D, Pedroarena C. The neuronal basis for consciousness. Philos Trans R Soc Lond B Biol Sci 1998; 353 1841–9.
| The neuronal basis for consciousness.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK1M%2FntFChsg%3D%3D&md5=925983c5930201b0f663e1752cdc4cc2CAS | 9854256PubMed |
[31] Harvey SM. Female sexual behavior: fluctuations during the menstrual cycle. J Psychosom Res 1987; 31 101–10.
| Female sexual behavior: fluctuations during the menstrual cycle.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaL2s7ktVyqtA%3D%3D&md5=2765932ee1be24eb7eff5de41bd3939eCAS | 3820137PubMed |