Suppr超能文献

勃起功能障碍药物改变了抗氧化酶的活性、氧化应激和参与类固醇激素甾体生成的某些细胞色素 P450 同工酶的蛋白表达。

Erectile dysfunction drugs altered the activities of antioxidant enzymes, oxidative stress and the protein expressions of some cytochrome P450 isozymes involved in the steroidogenesis of steroid hormones.

机构信息

Department of Clinical Biochemistry, Faculty of Medicine, King Khalid University, Abha, Kingdom of Saudi Arabia.

Department of Biotechnology, Alexandria University, Alexandria, Egypt.

出版信息

PLoS One. 2020 Nov 9;15(11):e0241509. doi: 10.1371/journal.pone.0241509. eCollection 2020.

Abstract

OBJECTIVES

Infertility is a global health problem with about 15 percent of couples involved. About half of the cases of infertility are related to male-related factors. A major cause of infertility in men is oxidative stress, which refers to an imbalance between levels of reactive oxygen species (ROS) and antioxidants. Erectile dysfunction drugs (EDD), known as phosphodiesterase inhibitors (PDEIs), have been used for the treatment of ED. It has been shown that oxidative stress plays an important role in the progression of erectile dysfunction. Oxidative stress can be alleviated or decreased by non-antioxidants and antioxidant enzymes. The present study was undertaken to determine if these compounds could have a role in the incidence of infertility, especially after long-term use. Therefore, the present study aims to investigate the effect of EDD on the activities of antioxidant enzymes, free radical levels as well as the protein expression of different cytochrome P450 isozymes involved in the steroidogenesis of different hormones. In addition, the activity of both 17β-hydroxysteroid dehydrogenase and 17-ketosteroid reductase were assayed. The architectures of both livers and testes cells were investigated under the influence of EDD.

METHODS

A daily dose of Sildenafil (1.48 mg/kg), Tadalafil (0.285 mg/kg) and Vardenafil (0.285 mg/kg) were administered orally to male rabbits for 12 week. Western immunoblotting, ELISA, spectrophotometric and histopathological techniques were used in this study.

RESULTS

The present study showed that Sildenafil, Vardenafil, and Tadalafil treatments significantly decreased the levels of glutathione and free radicals in both livers and testes of rabbits. Also, Vardenafil and Sildenafil induced the activity of superoxide dismutase and catalase whereas, glutathione S-transferase, glutathione reductase, and glutathione peroxidase activities inhibited in livers of rabbits. The protein expression of cytochrome P450 isozymes (CYP 11A1, 21A2, and 19C) which are involved in the steroidogenesis was markedly changed in both livers and testes of rabbits after their treatments for 12 weeks. After the treatment of rabbits with these medication, the protein expression of CYP11A1 was slightly down-regulated in both livers and testes except Sildenafil up-regulated such protein expression. In addition, the protein expressions of CYP11A1 and CYP 19C in both livers and testes were down-regulated after treatment of rabbits with Sildenafil, Vardenafil, and Tadalafil for 12 weeks. Also, these drugs inhibited the activity of both 17β-hydroxysteroid dehydrogenase and 17-ketosteroid reductase in testes of rabbits. Moreover, Sildenafil, Vardenafil, and Tadalafil-treated rabbits showed a decrease in spermatocytes and the number of sperms in the testes.

CONCLUSIONS

It is concluded that ED drugs induced the activities of both SOD and catalase which consequently decreased MDA level. Decrement in MDA levels and oxidative stress could therefore sustain the erection for a long period of time. On the other hand, it is not advised to use these drugs for a long-term since the protein expressions of CYP isozymes involved in steroidogenesis as well as the numbers of spermatocytes in testes were decreased.

摘要

目的

不孕是一个全球性的健康问题,大约 15%的夫妇受到影响。不孕的一半病例与男性相关因素有关。男性不育的一个主要原因是氧化应激,它是指活性氧(ROS)和抗氧化剂之间的失衡。勃起功能障碍药物(EDD),称为磷酸二酯酶抑制剂(PDEIs),已被用于治疗 ED。已经表明,氧化应激在勃起功能障碍的进展中起着重要作用。氧化应激可以通过非抗氧化剂和抗氧化酶来缓解或减少。本研究旨在确定这些化合物是否在不孕的发生中起作用,特别是在长期使用后。因此,本研究旨在研究 EDD 对不同激素类固醇生成中涉及的不同细胞色素 P450 同工酶的抗氧化酶活性、自由基水平以及蛋白质表达的影响。此外,还测定了 17β-羟固醇脱氢酶和 17-酮固醇还原酶的活性。研究了 EDD 对肝脏和睾丸细胞结构的影响。

方法

每天给雄性兔子口服西地那非(1.48mg/kg)、他达拉非(0.285mg/kg)和伐地那非(0.285mg/kg),连续 12 周。本研究采用 Western 免疫印迹、ELISA、分光光度法和组织病理学技术。

结果

本研究表明,西地那非、伐地那非和他达拉非治疗显著降低了兔子肝脏和睾丸中谷胱甘肽和自由基的水平。此外,伐地那非和西地那非诱导超氧化物歧化酶和过氧化氢酶的活性,而谷胱甘肽 S-转移酶、谷胱甘肽还原酶和谷胱甘肽过氧化物酶的活性在兔子肝脏中受到抑制。参与类固醇生成的细胞色素 P450 同工酶(CYP11A1、21A2 和 19C)的蛋白表达在兔子肝脏和睾丸中在治疗 12 周后明显改变。在这些药物治疗兔子 12 周后,除了西地那非上调了这种蛋白表达外,CYP11A1 的蛋白表达在肝脏和睾丸中都略有下调。此外,在西地那非、伐地那非和他达拉非治疗 12 周后,CYP11A1 和 CYP19C 在肝脏和睾丸中的蛋白表达均下调。此外,这些药物抑制了兔子睾丸中 17β-羟固醇脱氢酶和 17-酮固醇还原酶的活性。此外,西地那非、伐地那非和他达拉非治疗的兔子显示出精母细胞和睾丸中精子数量减少。

结论

总之,ED 药物诱导了 SOD 和过氧化氢酶的活性,从而降低了 MDA 水平。MDA 水平和氧化应激的降低因此可以维持长时间的勃起。另一方面,不建议长期使用这些药物,因为参与类固醇生成的细胞色素同工酶的蛋白表达以及睾丸中精母细胞的数量减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a487/7652355/91d8682822ad/pone.0241509.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验