Shilajit mitigates chemotherapeutic drug-induced testicular toxicity: Study on testicular germ cell dynamics, steroidogenesis modulation, and Nrf-2/Keap-1 signaling

IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE
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Abstract

Background

Medications, including chemotherapeutic drugs, contribute to male infertility as external factors by inducing oxidative stress in testicular cells. Shilajit is a naturally occurring bioactive antioxidant used in Ayurvedic medicine to treat a variety of ailments.

Objective

This study examines the potential of Shilajit to counteract the negative effects of the chemotherapeutic drug cyclophosphamide (CPA) on testicular germ cell dynamics.

Material and methods

Male Parkes mice received single intraperitoneal CPA injection (200 mg/kg BW) on day one, followed by daily supplementation of Shilajit (100 and 200 mg/kg BW) for one spermatogenic cycle.

Results

CPA adversely affected testicular germ cell dynamics by inhibiting the conversion of spermatogonia-to-spermatids, altering testicular histoarchitecture, impairing Sertoli cell function and testicular steroidogenesis, and disturbing the testicular oxido-apoptotic balance. Shilajit supplementation restores testicular germ cell dynamics in CPA-exposed mice, as evidenced by improved histoarchitecture of the testis. Shilajit improves testicular daily production and sperm quality by promoting the conversion of spermatogonia (2C) into spermatids (1C), stimulating germ cell proliferation (PCNA), improving Sertoli cell function (N-Cadherin and β-Catenin), and maintaining the Bax/Bcl2 ratio. Additionally, Shilajit enhances testosterone biosynthesis by activating enzymes like 3β-HSD, and 17β-HSD. Shilajit also reduces testicular oxidative stress by increasing antioxidant enzyme activity (SOD) and decreasing lipid peroxidation (LPO). These effects are mediated by upregulation of the antioxidant protein Nrf-2 and downregulation of Keap-1.

Conclusion

The findings underscore the potent androgenic and antioxidant characteristics of Shilajit, as well as its ability to enhance fertility in cases of testicular damage caused by chemotherapeutic drugs.

夏拉吉减轻化疗药物引起的睾丸毒性:睾丸生殖细胞动力学、类固醇生成调节和Nrf-2/Keap-1信号传导研究
背景:包括化疗药物在内的药物通过诱导睾丸细胞的氧化应激,作为外部因素导致男性不育。Shilajit是一种天然生物活性抗氧化剂,在阿育吠陀医学中被用于治疗多种疾病:本研究探讨了夏拉杰特抵消化疗药物环磷酰胺(CPA)对睾丸生殖细胞动力学负面影响的潜力:雄性Parkes小鼠在第一天腹腔注射单次CPA(200毫克/千克体重),然后每天补充Shilajit(100和200毫克/千克体重),持续一个生精周期:结果:CPA通过抑制精原细胞向精母细胞的转化、改变睾丸组织结构、损害Sertoli细胞功能和睾丸类固醇生成以及扰乱睾丸氧化-凋亡平衡,对睾丸生精细胞动力学产生了不利影响。睾丸组织结构的改善证明,补充夏拉杰特能恢复暴露于 CPA 的小鼠睾丸生殖细胞的活力。通过促进精原细胞(2C)转化为精子细胞(1C)、刺激生殖细胞增殖(PCNA)、改善Sertoli细胞功能(N-Cadherin和β-Catenin)以及维持Bax/Bcl2比率,夏拉吉提提高了睾丸的日产量和精子质量。此外,夏拉吉通过激活 3β-HSD 和 17β-HSD 等酶来增强睾酮的生物合成。夏拉吉提还能通过提高抗氧化酶活性(SOD)和降低脂质过氧化反应(LPO)来减少睾丸氧化应激。这些作用是通过上调抗氧化蛋白 Nrf-2 和下调 Keap-1 来实现的:结论:研究结果强调了夏拉杰特(Shilajit)的强效雄激素和抗氧化特性,以及在化疗药物导致睾丸损伤的情况下提高生育能力的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Ayurveda and Integrative Medicine
Journal of Ayurveda and Integrative Medicine INTEGRATIVE & COMPLEMENTARY MEDICINE-
CiteScore
4.70
自引率
12.50%
发文量
136
审稿时长
30 weeks
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