Protective Effects of Morus Alba (M.alba) Extract on the Alteration of Testicular Tissue and Spermatogenesis in Adult Rats Treated with Monosodium Glutamate

Various studies have confirmed toxic effects of monosodium glutamate in different organs. The review of literatures about influence of MSG on the male reproductive system shows the variety of tissue damages. Most of these changes mainly manifested by increased oxidative stress and cytotoxicity. The present study was aimed to investigate the possible protective effects of herbal antioxidants (Morus Alba) on the tissue damages related to monosodium glutamate cytotoxicity. Forty-eight adult Wistar rats were divided into two control and experimental groups. Each group divided into short (14 days) and long term (28 days) group. Experimental group was subdivided into four subgroups. The experimental group was injected with MSG (4 mg/kg BW, i.p.). Morus Alba extract (100 mg/kg BW) was administrated to two MSG treated experimental subgroups. At the end of study, the right testis was processed for histological evaluation and the left one was processed for sperm analysis and morphometric studies. Decrease of spermatogenic indices was accompanied with the changes in histomorphology of seminiferous tubules in MSG treated groups. Moreover, the sperm analysis indices were decreased in MSG treated rats. These changes were more obvious in long term treatments. The administration of Morus Alba extract led to improvement in histologic and spermatogenic indices. The most observable improvement in tissue changes was obtained by long term treatment with Morus Alba extract. The present study suggests that the administration of Morus Alba extract can preserve the positive effects in reduction of testicular tissue alterations in Monosodium glutamate tissue toxicity.

___

1. Moore KL. Congenital malformations due to environment. In: Developing Humans. 2nd edition. WB Saunders co Ltd, Philadelphia, 2003;173-83.

2. Adrienne S. The toxicity-safety of MSG. Acct Res. 1999;6(4):259-310.

3. Andrew OE. Histological studies of the effects of monosodium glutamate on the kidney of adult wistar rats. Internet J Health. 2007;6(2):1.

4. Miksowiak B, Partyka M. Effects of neonatal treatment with MSG (monosodium glutamate) on hypothalamo-pituitary-thyroid axis in adult male rats. Histol Histopathol. 1993;8(4):731-4.

5. Mozes S, Sefeikova Z. Obesity and changes of alkaline phosphatase activity in the small intestine of 40 and 80-day old rats subjected to early postnatal overfeeding of monosodium glutamate. Physiol Res. 2004;53(2):177-86.

6. Onakewhor JUE, Oforofuo IAO, Singh SP. Chronic administration of monosodium glutamate induces oligozoospermia and glucogen accumulation in wistar rat testes. Africa J Reprod Health. 1998;2(2):190-7.

7. Pizzi WJ, Barnhart JE, Unnerstall JR. Reproductive dysfunction in male rats following neonatal administration of monosodium L-glutamate. Neurobehav Toxicol. 1979;1(1):1-4.

8. Oforofuo IAO, Onakewhor JUE, Idaewor PE. The effect of chronic administration of MSG on the histology of the adult wistar rat testis. Biosci Res Comm. 1997;9(2):1-2.

9. Zhang W, Han F, He J, Duan C. HPLC-DAD-ESI-MS/MS analysis and antioxidant activities of nonanthocyanin phenolics in mulberry (Morus alba L.). J Food Sci. 2008;73(6):C512-C518.

10. Yang X, Yang L, Zheng H. Hypolipidemic and antioxidant effects of mulberry (Morus alba L.) fruit in hyperlipidaemia rats. Food Chem Toxicol. 2010;48(8-9):2374-9.

11. Wang Y, Xiang L, Wang C, Tang C, He X. Antidiabetic and antioxidant effects and phytochemicals of Mulberry fruit (Morus alba L.) polyphenol enhanced extract. PLoS ONE. 2013;8(7):e71144.

12. Kim SB, Chang BY, Jo YH, Lee SH, Han SB, Hwang BY, Kim SY, Lee MK. Macrophage activating activity of pyrrole alkaloids from Morus alba fruits. J Ethnopharmacol. 2013;145(1):393-6.

13. Asano N, Yamashita T, Yasuda K, Ikeda K, Kizu H, Kameda Y, Kato A, Nash RJ, Lee HS, Ryu KS. Polyhydroxylated alkaloids isolated from mulberry trees (Morus alba L.) and silkworms (Bombyx mori L.). J Agric Food Chem. 2001;49(9):4208-13.

14. Narayana K, Prashanthi N, Nayanatara A, Kumar HH, Abhilash K, Bairy KL. Neonatal methyl parathion exposure affects the growth and functions of the male reproductive system in the adult rat. Folia Morphol. 2005;65(1):26-33.

15. Nayatara, AK, Vinodini NA, Damodar G, Ahmed B, Ramaswamy CR, Shabarienth S. Role of ascorbic acid in monosodium glutamate mediated effect on testicular weight, sperm morphology and sperm count in rat testis. J Chin Clin Med. 2008;3(1):1-5.

16. Nosseir NS, Ali MHM, Ebaid HM. A Histological and morphometric study of monosodium glutamate toxic effect on testicular structure and potentiality of recovery in adult albino rats. Res J Biol. 2012;2(2):66-78.

17. Meistrich M, Wilson G, Porter K. Restoration of spermatogenesis in DBCP-treated rats by hormone suppression. Toxicol Sci. 2003;76(2):418-26.

18. Wyrobek AJ, Gordon LA, Burkhart JG, Francis MW, Kapp RW Jr, Letz G, Malling HV, Topham JC, Whorton MD. An evaluation of the mouse sperm morphology test and other sperm tests in nonhuman mammals. A report of the US environmental protection agency gene-tox program. Mutat Res. 1983;115(1):1-72.

19. Marcia C. Masculinity, Reproduction and male infertility in the Middle East. J. Mid East Women Stud. 2007;3(3):1-20.

20. Redding TW, Schally AV, Arimura A, Wakabayashi I. Effect of monosodium glutamate on some endocrine functions. Neuroendocrinol. 1971;8(3):245-55.

21. Pizzi WJ, Barnhart JE, Fanslow DJ. Monosodium glutamate administration to the newborn reduces reproductive ability in female and male mice. Science. 1977;196(4288):452-4.

22. Velioglu YS, Mazza G, Gao L, Oomah BD. Antioxidant activity and total phenolics in selected fruits, vegetables, and grain products. J Agric Food Chem. 1998;46(10):4113- 7.

23. Nishikawa T, Araki E. Impact of mitochondrial ROS production in the pathogenesis of diabetes mellitus and its complications. Antioxid Redox Signal. 2007; 9(3):343-53.

24. Shrilatha B, Muralidhara. Early oxidative stress in testis and epididymal sperm in streptozotocin-induced diabetic mice: its progression and genotoxic consequences. Reprod Toxicol. 2007:23(4):578-87.

25. Aitken RJ, Roman SD. Antioxidant systems and oxidative stress in the testes. Oxid Med Cell Longev. 2008;1(1):15-24.

26. Maiorino M, Ursini F. Oxidative Stress, spermatogenesis and fertility. Biol Chem. 2005;383(3-4):591-7.

27. Reddy MM, Mahipal VKS, Subhashini J, Reddy CM, Roy RK, Reddy VG, Reddy RKP, Reddanna P. Bacterial lipopolysaccharide-induced oxidative stress in the impairment of steroidogenesis and spermatogenesis in rats. Reprod Toxicol. 2006;22(3):493-500.
Medicine Science-Cover
  • ISSN: 2147-0634
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 2012
  • Yayıncı: Effect Publishing Agency ( EPA )