Testicular cytoprotective effect of glucagon like peptide-1 in diabetic rats involves inhibition of apoptosis, endoplasmic reticulum stress and activation of autophagy

被引:6
作者
Abdel-Hakeem, Elshymaa A. [1 ,4 ]
Zenhom, Nagwa M. [2 ]
Mokhemer, Sahar A. [3 ]
机构
[1] Minia Univ, Fac Med, Dept Med Physiol, Al Minya, Egypt
[2] Minia Univ, Fac Med, Dept Med Biochem, Al Minya, Egypt
[3] Minia Univ, Fac Med, Dept Histol & Cell Biol, Al Minya, Egypt
[4] Minia Univ, Fac Med, Med Physiol Dept, Al Minya 61111, Egypt
关键词
GLP-1; Exenatide; Diabetes; Testicular dysfunction; Autophagy; AMPK; MALE REPRODUCTIVE FUNCTION; HIGH-FAT DIET; OXIDATIVE STRESS; EXPRESSION; RECEPTOR; DAMAGE; KISSPEPTIN; PATHWAYS;
D O I
10.4149/gpb_2022064
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study aimed to explore the possible cytoprotective effects of exenatide, a glucagon-like peptide-1 (GLP-1) receptor agonist, in the testicles of diabetic rats. Exenatide has numerous advanta-geous properties in addition to its hypoglycemic effect. However, its impact on testicular tissue in diabetes needs more clarification. Therefore, rats were divided into control, exenatide-treated, diabetic and exenatide-treated diabetic groups. Blood glucose and serum levels of insulin, testosterone, pituitary gonadotropins and kisspeptin-1 were measured. Real-time PCR for beclin-1, p62, mammalian target of rapamycin (mTOR), and AMP-activated protein kinase (AMPK), were estimated in testicular tis-sue in addition to markers of oxidative stress, inflammation, and endoplasmic reticulum stress. Also, immuno-expression of protein P53, nuclear erythroid factor2 (Nrf2) and vimentin was conducted. Exenatide was able to attenuate diabetic toxic changes and enhance autophagy in testicular tissue. These results indicate the protective effect of exenatide against diabetic testicular dysfunction.
引用
收藏
页码:135 / 148
页数:14
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