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Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

145 Inhibitory effects of gossypol on bovine in vitro embryo production

L. K. Hatamoto-Zervoudakis A , M. F. Duarte Jr. A , T. F. Motheo A , P. P. Tsuneda A and J. T. Zervoudakis A
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Faculty of Veterinary Medicine, Federal University of Mato Grosso, UFMT, Cuiabá, Mato Grosso, Brazil

Reproduction, Fertility and Development 31(1) 197-198 https://doi.org/10.1071/RDv31n1Ab145
Published online: 3 December 2018

Abstract

Cottonseed and its derivatives are frequently used in cattle feed as an effective dietary fibre supply and high protein and energy food source. However, the cotton plant contains gossypol, which in its free form induces male and female infertility. Therefore, this study aimed to evaluate the effect of gossypol supplementation on bovine in vitro embryo production. Ovaries were retrieved from slaughterhouses, and cumulus-oocyte complexes (COC) were recovered by follicular puncture. Based on free gossypol concentration present on the in vitro maturation, sperm capacitation, IVF and in vitro culture media, grades I, II and III COC (n = 646) were divided in 3 treatments: 0 μg mL−1 (control), 5 μg mL−1 (G5) and 10 μg mL−1 (G10). The COC were matured under a humidified atmosphere of 5% CO2 in air at 38.5°C for 24 h in 90-μL droplets containing TCM-199 supplemented with 10% FCS, 0.2 mM sodium pyruvate, LH, FSH, 75 μg mL−1 amikacin, 17β-oestradiol. Each droplet corresponded to one replicate (n = 14) and contained 15 to 18 COC. Matured COC and sperm were co-incubated in droplets (8-13 COC per 90 μL) of TALP-IVF media supplemented with 6 mg mL−1 BSA, 0.2 mM sodium pyruvate, 30 μg mL−1 heparin, 20 μM penicillamine, 10 μM hypotaurine, 1 μM epinephrine, 75 μg mL−1 amikacin under a 5% CO2 humidified atmosphere at 38.5°C, for 20 h. For IVF, non-sexed frozen-thawed semen was selected with Percoll® gradient. The resulting pellet was subjectively evaluated for motility and concentration and then diluted to final concentration of sperm mL−1 with fertilization medium. Presumptive zygotes were then cultured in 90-μL droplets of SOFaaci medium supplemented with 2.7 mM myo-inosytol, 0.2 mM pyruvate, 2.5% FCS (v/v), 5 mg mL−1 BSA, 75 μg mL−1 amikacin, and maintained for 8 days at 38.5°C in a humidified atmosphere with 5% CO2 in air. Cleavage, blastocysts production and hatching rates were evaluated at Days 3, 7 and 8, respectively. Data were submitted to ANOVA for parametric data and Wilcoxon test for non-parametric variables using the SAS software (SAS Institute Inc., Cary, NC, USA). Significance level was set at 5%. Cleavage rates of the control (81.05%) and G5 (71.85%) were higher compared with G10 (19.64%; P < 0.0001). Blastocyst production was lower in G5 (12.18%) compared with control (30.35%), and the addition of 10 μg mL−1 of free gossypol (G10) completely inhibited embryo development (0%; P < 0.0001). As for the percentage of hatched blastocysts, the control (66.75%) had greater values compared with G5 (34.52%; P < 0.0001). Thus, the addition of 5 and 10 μg mL−1 of free gossypol are extremely hazardous for in vitro bovine embryo development. Whether these deleterious effects take place in a similar fashion during in vivo embryo production remains to be investigated.