Beta(β)-sitosterol attenuates Chronic Unpredictable Stress (CUS) Induced Testicular Damage in the Experimental Rat Model

被引:0
|
作者
Singh, Jiten [1 ,2 ]
Srivastava, Siddhi [1 ]
Zehra, Areesh [1 ]
Prajapati, Priyanka [1 ]
Agarwal, Vipul [1 ]
Kumar, Anand [4 ]
Mishra, Vikas [1 ]
Kushwaha, Sapana [3 ]
机构
[1] Babasaheb Bhimrao Ambedkar Univ, Sch Pharmaceut Sci, Dept Pharmaceut Sci, Raebareli Rd, Lucknow 226025, India
[2] Cent Univ Haryana, Sch Interdisciplinary Sci, Dept Pharmaceut Sci, Mahendergarh 123031, India
[3] Natl Inst Pharmaceut Educ & Res, Dept Pharmacol & Toxicol, Raebareli NIPER R, Lucknow 226002, India
[4] Cent Univ Rajasthan, Dept Pharm, Sch Chem Sci & Pharm, Ajmer 305817, Rajasthan, India
关键词
Chronic unpredictable stress; beta-sitosterol; Rat; Fibronectin type III domain-containing protein 5 (FNDC5); Cytochrome P450 side-chain cleavage enzyme (P450scc); 3-beta hydroxysteroid dehydrogenase (3 beta-HSD); Testicular damage; BETA-SITOSTEROL; OXIDATIVE STRESS; IRISIN; BEHAVIORS; EXPOSURE; EXERCISE;
D O I
10.1007/s43032-025-01825-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Chronic stress is a major contributor to male reproductive dysfunction leading to testicular damage and impaired spermatogenesis. This study investigates the protective effects of beta-sitosterol, a phytosterol with known antioxidant properties, against CUS-induced testicular damage in rats. Male Wistar rats were divided into Control, Chronic Unpredictable Stress (CUS), and CUS + beta-sitosterol. The CUS and CUS + beta-sitosterol groups were exposed to random stressors for eight weeks. beta-Sitosterol was administered orally at a dose of 20 mg/kg for three weeks, starting from the fifth week of CUS induction. Behavioral tests like EPMT and NSFT were conducted to confirm CUS induction, after which serum, testis, and epididymis samples were collected for analysis. beta-sitosterol significantly increased testis and epididymis weight, along with sperm counts in CUS rats. Histological analysis revealed restoration of testicular cellular structure, as indicated by an improved Johnsen's index scores. Additionally, beta-sitosterol restored antioxidant levels and oxidative stress parameters in testicular tissue. TEM showed germ cell integrity and restored basement membrane structure in the CUS + beta-sitosterol group. In silico analysis indicated strong interactions of beta-sitosterol with FNDC5, P450scc, and 3 beta-HSD proteins involved in steroidogenesis. Immunohistochemistry confirmed an increased expression of FNDC5 in the CUS + beta-sitosterol group, beta-sitosterol ameliorates CUS-induced testicular damage and improves sperm count, highlighting its potential as a dietary intervention for stress-related male infertility. Further preclinical and clinical studies are warranted to explore its therapeutic potential.
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页数:19
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