白球花提取物对bps诱导的大鼠睾丸损伤的保护作用是通过下调ripk1 /3- mlk驱动的坏死下垂和fas - fasl介导的细胞凋亡来实现的

IF 1.3 Q3 PHARMACOLOGY & PHARMACY
Shabnoor Iqbal, Timothy Omara, Ivan Kahwa, Usman Mir Khan
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引用次数: 0

摘要

双酚S (BPS)是制造聚碳酸酯塑料的首选单体之一。结果表明,Sphaeranthus indicus花提取物(Sphaeranthus indicus flower extract, SFE)对BPS(50µg/kg /体重)对大鼠生殖毒性的保护作用与双酚a相似。不同剂量的SFE(25、50和100 mg/kg)灌胃10周。高效液相色谱(HPLC)结果表明,SFE中含有丰富的多酚类物质,其中芦丁和槲皮素是调节bps诱导的坏死坏死和细胞凋亡的重要生物活性分子。生化分析显示,给予BPS的大鼠仅表现出氮氧化应激、坏死(RIPK1/RIPK3和MLKL)和凋亡介质(Fas/FasL和caspase 3/caspase-8)的生物标志物显著升高。这些事件引起了大鼠精子特征(精子活力、精子头和精子活力)、精子数量和激素特征(促甲状腺激素、促黄体激素和促卵泡激素)的变化。组织学分析表明,支持细胞明显脱落,生精细胞密度降低,精小管水平升高,精小管相关形态学参数紊乱。在含bps水的大鼠中补充SFE可以恢复氮氧化应激生物标志物,从而减少坏死和细胞凋亡。补充SFE后,所有氧化应激、炎症、坏死性下垂和细胞凋亡的生物标志物恢复了睾丸的激素水平和正常的组织结构。虚拟筛选结果表明,ripk3 -芦丁和ripk1 -槲皮素复合物是坏死性坏死的关键调控因子。需要进一步的研究来评估其药效学、动力学和人类日常使用的有效浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective effects of Sphaeranthus indicus floral extract against BPS-induced testicular damage in rats occurs through downregulation of RIPK1/3-MLK-driven necroptosis and Fas-FasL-mediated apoptosis

Bisphenol S (BPS) is one of the monomers preferred in the manufacturing of polycarbonate plastics. Unfortunately, its estrogenic and genotoxic effects are similar to those of bisphenol A. The protective effects of Sphaeranthus indicus floral extract (SFE) against reprotoxic effects of BPS (50 µg/kg per body weight) in rats exposed to it via drinking water was investigated. Different SFE doses (25, 50, and 100 mg/kg) were administered via oral gavage for 10 weeks. High-performance liquid chromatography (HPLC) results indicated that SFE was rich in polyphenols, with rutin and quercetin being important bioactive molecules modulating BPS-induced necroptosis and apoptosis. Biochemical analyses unveiled that rats administered BPS only exhibited considerable elevation of biomarkers of nitro-oxidative stress, necroptotic (RIPK1/RIPK3 and MLKL), and apoptotic mediators (Fas/FasL and caspase 3/caspase-8). These events caused changes in sperm characteristics (sperm motility, sperm head, and sperm viability), sperm count, and hormonal profile (thyroid stimulating hormone, luteinizing hormone, and follicle-stimulating hormone) of the rats. Histological analysis suggested that there was pronounced sloughing of Sertoli cells, reduced spermatogenic cell density, increased levels of seminiferous tubules, and disorganized morphometric parameters related to seminiferous tubules. The SFE supplementation in rats with BPS-containing water restored nitro-oxidative stress biomarkers, which led to the reduction of necroptosis and apoptosis. Reinstatement of all the biomarkers of oxidative stress, inflammation, necroptosis, and apoptosis after SFE supplementations restored the hormonal profile and normal histoarchitecture of the testes. Virtual screening elucidated that the key regulators of the necroptosis are RIPK3-rutin and RIPK1-quercetin complexes. Further studies are needed to assess its pharmacodynamics, kinetics, and effective concentration for daily use in humans.

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来源期刊
Advances in Traditional Medicine
Advances in Traditional Medicine PHARMACOLOGY & PHARMACY-
CiteScore
4.30
自引率
0.00%
发文量
50
期刊介绍: Advances in Traditional Medicine (ADTM) is an international and peer-reviewed journal and publishes a variety of articles including original researches, reviews, short communications, and case-reports. ADTM aims to bridging the gap between Traditional knowledge and medical advances. The journal focuses on publishing valid, relevant, and rigorous experimental research and clinical applications of Traditidnal Medicine as well as medical classics. At the same time, the journal is devoted to communication among basic researcher and medical clinician interested in the advancement of Traditional Medicine. Topics covered by the journal are: Medical Classics & History; Biomedical Research; Pharmacology & Toxicology of Natural Products; Acupuncture & Moxibustion; Sasang Constitutional Medicine; Diagnostics and Instrumental Development; Clinical Research. ADTM is published four times yearly. The publication date of this journal is 30th March, June, September, and December.
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