Combined effects of arsenic exposure and diabetes on male reproductive functions.

作者: A. C. F. Souza , D. S. S. Bastos , M. N. Sertorio , F. C. Santos , L. O. G. Ervilha

DOI: 10.1111/ANDR.12613

关键词:

摘要: Background It is known that exposure to either arsenic or hyperglycemia can induce male reproductive damages. However, their combined effects on organs are still unclear. Therefore, the present study investigated morphological and functional parameters of testis, epididymis, spermatozoa in diabetic rats exposed arsenate. Materials methods Diabetes was induced by intraperitoneal streptozotocin injection. While a set healthy animals received saline solution (negative control diabetes control, respectively), other 10 mg/L sodium arsenate (arsenic + groups, respectively) for 40 days drinking water. Testosterone concentration, daily sperm production, counts testis were evaluated groups. Moreover, epididymis subjected antioxidant enzymes analysis, micromineral determination, histopathological evaluation. Results Arsenate reduced serum testosterone concentration worsened this reduction rats. In addition, number tissues, as well decreased these Sperm such motility, morphology, integrity acrosomal plasma membranes impaired health The combination arsenate, turn, increased only percentage with abnormal morphology. proportion both groups receiving Its bioaccumulation caused an imbalance activities mineral content animals, enhancing changes Testicular pathologies occurred mainly co-exposed Conclusion Our results indicate enhances several damages functions rats, impairing levels inducing nitrosative stress epididymis.

参考文章(53)
Narendra Mohan Biswas, Gargi Ray Chaudhuri, Aloke Chattopadhyay, Mahitosh Sarkar, Effect of sodium arsenite on spermatogenesis, plasma gonadotrophins and testosterone in rats. Asian Journal of Andrology. ,vol. 5, pp. 27- 31 ,(2003)
L. Seethalakshmi, M. Menon, D. Diamond, The Effect of Streptozotocin-Induced Diabetes on the Neuroendocrine-Male Reproductive Tract Axis of the Adult Rat The Journal of Urology. ,vol. 138, pp. 190- 194 ,(1987) , 10.1016/S0022-5347(17)43042-4
Hugo Aebi, Catalase in vitro Methods in Enzymology. ,vol. 105, pp. 121- 126 ,(1984) , 10.1016/S0076-6879(84)05016-3
Kenneth K. Wu, Youming Huan, Streptozotocin‐Induced Diabetic Models in Mice and Rats Current Protocols in Pharmacology. ,vol. 40, ,(2008) , 10.1002/0471141755.PH0547S40
Rodney L. Levine, Donita Garland, Cynthia N. Oliver, Adolfo Amici, Isabel Climent, Anke-G. Lenz, Bong-Whan Ahn, Shmuel Shaltiel, Earl R. Stadtman, Determination of carbonyl content in oxidatively modified proteins. Methods in Enzymology. ,vol. 186, pp. 464- 478 ,(1990) , 10.1016/0076-6879(90)86141-H
William H. Habig, Michael J. Pabst, William B. Jakoby, Glutathione S-Transferases Journal of Biological Chemistry. ,vol. 249, pp. 7130- 7139 ,(1974) , 10.1016/S0021-9258(19)42083-8
John A. Buege, Steven D. Aust, Microsomal lipid peroxidation. Methods in Enzymology. ,vol. 52, pp. 302- 310 ,(1978) , 10.1016/S0076-6879(78)52032-6
Iwona Zwolak, Halina Zaporowska, Selenium interactions and toxicity: a review. Selenium interactions and toxicity. Cell Biology and Toxicology. ,vol. 28, pp. 31- 46 ,(2012) , 10.1007/S10565-011-9203-9
Michael F Hughes, Arsenic toxicity and potential mechanisms of action Toxicology Letters. ,vol. 133, pp. 1- 16 ,(2002) , 10.1016/S0378-4274(02)00084-X
George L. King, Mary R. Loeken, Hyperglycemia-induced oxidative stress in diabetic complications. Histochemistry and Cell Biology. ,vol. 122, pp. 333- 338 ,(2004) , 10.1007/S00418-004-0678-9