香芹酚对甲基苯丙胺处理大鼠睾丸组织P53蛋白表达及精子发生的影响

Thrita Pub Date : 2019-01-22 DOI:10.5812/THRITA.88303
M. Farhadi, B. Jameie, Parisa Honarkaran, Raheleh Mollajani, M. Jameie, Melikasadt Jameie
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引用次数: 1

摘要

在发达社会,传统和工业成瘾药物的应用正在扩大。香芹酚广泛用于传统医学,甲基苯丙胺直接或间接地影响所有器官。根据甲基苯丙胺的作用机制,近年来研究了抗氧化剂的治疗作用,以减少甲基苯丙胺滥用的后果。本研究旨在探讨香芹酚对甲基苯丙胺处理大鼠精子发生的抗凋亡作用。将32只成年雄性大鼠随机分为阳性对照组、阴性对照组、假手术组和实验组。采用苏木精和伊红染色技术检测生精细胞和睾丸组织,Western blotting检测P53表达作为诱导凋亡的因子。目前的研究数据显示,在阳性对照组中,甲基苯丙胺显著减少了生精细胞,而在实验组中,香芹酚增加了生精细胞。与阳性对照组相比,carvacrol降低了P53的表达(P < 0.05)。因此,香芹酚通过抑制P53蛋白表达而具有抗凋亡作用。总的来说,香芹酚可以减少一些与甲基苯丙胺滥用有关的常见症状,包括不孕症和诱导细胞凋亡。
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The Effect of Carvacrol on the Expression of P53 Protein in Testicular Tissue and Spermatogenesis of Rats Treated with Methamphetamine
The application of traditional and industrial addictive drugs is expanding in the developed societies. Carvacrol is widely used in traditional medicine, and methamphetamine, directly and indirectly, affects all organs. According to the mechanism of methamphetamine, the therapeutic effects of antioxidants were recently considered in order to reduce methamphetamine abuse outcomes. The current study aimed at evaluating the anti-apoptotic effect of carvacrol on spermatogenesis of rats treated with methamphetamine. Thus, 32 adult male rats were randomly divided into four groups: positive control, negative control, sham, and experimental. Spermatogenic cells and testis tissue were evaluated using hematoxylin and eosin staining technique and the expression of P53 was assessed by Western blotting as a factor to induced apoptosis. The current study data showed that methamphetamine significantly reduced spermatogenic cells in the positive control group, while carvacrol increased these cells in the experimental group. Also, carvacrol decreased P53 expression in the experimental group compared with the positive control group (P < 0.05). Therefore, carvacrol had an anti-apoptotic effect by suppressing P53 protein expression. Altogether, carvacrol can reduce some of the common symptoms related to methamphetamine abuse including infertility and induction of apoptosis.
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