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Taro flour (Colocasia esculenta) increases testosterone levels and gametogenic epithelium of Wistar rats

Published online by Cambridge University Press:  21 March 2018

G. G. Ribeiro*
Affiliation:
The Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, College of Nutrition, Federal Fluminense University, Braga, Brazil
L. R. Pessôa
Affiliation:
The Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, College of Nutrition, Federal Fluminense University, Braga, Brazil
M. D. C. de Abreu
Affiliation:
The Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, College of Nutrition, Federal Fluminense University, Braga, Brazil
L. B. N. S. Corrêa
Affiliation:
Department of Morphology, Biomedical Institute, Fluminense Federal University, Hernani Melo, Brazil
A. D’Avila Pereira
Affiliation:
The Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, College of Nutrition, Federal Fluminense University, Braga, Brazil
M. A. Chagas
Affiliation:
Department of Morphology, Biomedical Institute, Fluminense Federal University, Hernani Melo, Brazil
F. Z. Brandão
Affiliation:
Laboratory of Hormonal Dosage, Faculty of Veterinary Medicine, Fluminense Federal University, Filho, Brazil
C. A. S. da Costa
Affiliation:
The Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, College of Nutrition, Federal Fluminense University, Braga, Brazil
G. T. Boaventura
Affiliation:
The Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, College of Nutrition, Federal Fluminense University, Braga, Brazil
*
Address for correspondence: G. G. Ribeiro, Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, College of Nutrition, Fluminense Federal University, Rua Mário Santos Braga, 30, Niterói, RJ, 24015-110, Brazil. E-mail: [email protected]

Abstract

This study evaluated the effects of diet containing taro flour on hormone levels and the seminiferous tubules morphology of rats. After weaning, the male rats were divided into two groups (n=12 each): control group (CG) treated with control diet and taro group (TG), fed with 25% taro flour for 90 days. Food, caloric intake, mass and body length were evaluated at experiment end. Testis followed the standard histological processing. Immunostaining was performed using an anti-vimentin antibody to identify Sertoli cells. In histomorphometry, total diameter, total area, epithelial height, luminal height and luminal area were analyzed. The testosterone levels were performed using the radioimmunoassay method. Group TG presented (P<0.05): increase in mass, body length, testicular weight, histomorphometric parameters and hormonal levels. Food intake, calorie and Sertoli cells not presented statistical differences. The taro promoted increase in the testicles parameters and hormones.

Type
Brief Report
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2018 

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References

1. Pereira, FHF, Puiatti, M, Miranda, GV, et al. Genetic diversity in taro accessions. Hortic Bras. 2004; 22, 5560.Google Scholar
2. Chan, YC, Hsu, CK, Wang, MF, Su, TY. A diet containing yam reduces the cognitive deterioration and brain lipid peroxidation in mice with senescence accelerated. Int J Food Sci Technol. 2004; 39, 99107.Google Scholar
3. Depypere, HT, Comhaire, FH. Herbal preparations for the menopause: beyond isoflavones and black cohosh. Maturitas. 2014; 77, 191194.Google Scholar
4. Wu, WH, Liu, LY, Chung, CJ, Jou, HJ, Wang, TA. Estrogenic effect of yam ingestion in healthy postmenopausal women. J Am Coll Nutr. 2005; 24, 235243.Google Scholar
5. Chiang, SS, Chang, SP, Pan, TM. Osteoprotective effect of monascus-fermented dioscorea in ovariectomized rat model of postmenopausal osteoporosis. J Agric Food Chem. 2011; 59, 91509157.Google Scholar
6. Jianfeng, C, PengYing, Z, ChengWei, X, et al. Effect of aqueous extract of Arctium lappa L. (burdock) roots on the sexual behavior of male rats. BMC Complement Altern Med. 2012; 12, 18.Google Scholar
7. Gauthaman, K, Ganesan, AP. The hormonal effects of Tribulus terrestris and its role in the management of male erectile dysfunction – an evaluation using primates, rabbit and rat. Phytomedicine. 2008; 15, 4454.Google Scholar
8. Schaffer, S, Halliwell, B. Do polyphenols enter the brain and does it matter? Some theoretical and pratical considerations. Genes Nutr. 2012; 7, 99109.Google Scholar
9. Pessôa, LR, Rêgo, TS, Asht, LS, et al. Serum and liver lipids distributions in streptozotocin induced diabetic rat treated with diet containing Yam (Dioscorea bulbifera) flour. Nutr Hosp. 2015; 31, 16471653.Google Scholar
10. Reeves, PG. Components of the AIN-93 diets as improvements in the AIN-76A diet. J Nutr. 1997; 127, 838841.Google Scholar
11. Chan, YC, Hsu, CK, Wang, MF, et al. Beneficial effect of yam on the amyloid senescence β-protein, monoamine oxidase B and cognitive deficit in mice with accelerated. J Sci Food Agric. 2006; 86, 15171525.Google Scholar
12. Hashimoto, N, Noda, T, Kim, SJ, et al. Yam contributes to improvement of glucose metabolism in rats. Plant Foods Hum Nutr. 2009; 64, 193198.Google Scholar
13. Leblond, CP, Clermont, Y. Definition of the stages of the cycle of the seminiferous epithelium in the rat. Ann N Y Acad Sci. 1953; 55, 548573.Google Scholar
14. Sinha-Hikin, AP, Amador, AG, Klemcke, HG, et al. Correlative morphology and endocrinology of Sertoli cells in hamster testes in active and inactive states of spermatogenesis. Endocrinology. 1989; 125, 18291843.Google Scholar
15. Takashiba, KS, Segatelli, TM, Moraes, SMF, et al. Testicular morphology in obese and sedentary Wistar rats submitted to physical training. Acta Sci Health Sci. 2011; 33, 2533.Google Scholar
16. Goel, HC, Samanta, N, Kannan, K, et al. Protection of spermatogenesis in mice against gamma ray induced damage by Hippophae rhamnoides . Andrologia. 2006; 38, 199207.Google Scholar
17. Rafiee, FM, Nejati, V, Heidari, R, et al. Protective effect of methanolic extract of Berberis integerrima Bunge. Root on carbon tetrachloride-induced testicular injury in Wistar rats. Int J Reprod BioMed. 2016; 14, 133140.Google Scholar
18. Vyas, NY, Raval, MA. Aphrodisiac and spermatogenic potential of alkaloidal fraction of Hygrophila spinosa T. Ander in rats. J Ethnopharmacol. 2016; 194, 947953.Google Scholar
19. Wu, L, Dong, H, Zhao, J, et al. Diosgenin stimulates rat TM4 cell proliferation through activating plasma membrane translocation and transcriptional activity of estrogen receptors. Biol Reprod. 2015; 92, 110.Google Scholar
20. Monet-Kuntz, C, Hochereau-de Reviers, MT, Terqui, M. . Variations in testicular androgen receptors and histology of the lamb testis from birth to puberty. J Reprod Fertil. 1984; 70, 203210.Google Scholar