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肌动蛋白失调介导决明子水提取物的肾毒性。

Actin Dysregulation Mediates Nephrotoxicity of Cassiae Semen Aqueous Extracts.

作者信息

Yang Jinlan, Xiao Sheng, Li Ludi, Zhu An, Xiao Wusheng, Wang Qi

机构信息

Department of Toxicology, School of Public Health, Peking University, Beijing 100191, China.

Key Laboratory of State Administration of Traditional Chinese Medicine (TCM) for Compatibility Toxicology, Peking University, Beijing 100191, China.

出版信息

Toxics. 2024 Jul 30;12(8):556. doi: 10.3390/toxics12080556.

Abstract

semen, commonly consumed as roasted tea, has been widely used for both medicinal purposes and dietary supplements. In this study, we investigated the nephrotoxic effects and underlying mechanisms of semen aqueous extracts (CSAEs) using computational and animal models. Both male and female Sprague Dawley rats were treated with 4.73-47.30 g/kg (body weight) of CSAEs by oral gavage twice a day for 7-28 days. We found that serum and urinary biomarkers of kidney injury and kidney coefficients were increased in a dose-dependent manner, and were accompanied by morphological alterations in the kidneys of CSAEs-treated rats. Computational and molecular docking approaches predicted that the three most abundant components of CSAEs-obtusifolin, aurantio-obtusin, and obtusin-exhibited strong affinity for the binding of F-actin, ROCK1, and Rac1, and the RhoA-ROCK pathway was identified as the most likely regulatory mechanism mediating the nephrotoxicity of CSAEs. Consistently, immunofluorescence staining revealed F-actin and cytoskeleton were frequently disturbed in renal cells and brush borders at high doses of CSAEs. Results from gene expression analyses confirmed that CSAEs suppressed the key proteins in the RhoA-ROCK signaling pathway and consequently the expression of F-actin and its stabilization genes. In summary, our findings suggest that Cassiae semen can depolymerize and destabilize actin cytoskeleton by inhibition of the RhoA-ROCK pathway and/or direct binding to F-actin, leading to nephrotoxicity. The consumption of semen as a supplement and medicine warrants attention.

摘要

决明子,通常作为炒制茶饮来饮用,已被广泛用于药用和膳食补充剂。在本研究中,我们使用计算机模型和动物模型研究了决明子水提取物(CSAEs)的肾毒性作用及其潜在机制。将雄性和雌性Sprague Dawley大鼠每天经口灌胃给予4.73 - 47.30 g/kg(体重)的CSAEs,每日两次,持续7 - 28天。我们发现,肾脏损伤的血清和尿液生物标志物以及肾脏系数呈剂量依赖性增加,并且在接受CSAEs处理的大鼠肾脏中伴有形态学改变。计算机和分子对接方法预测,CSAEs中含量最高的三种成分——钝叶决明素、橙黄决明素和决明素——对F - 肌动蛋白、ROCK1和Rac1的结合表现出很强的亲和力,并且RhoA - ROCK途径被确定为介导CSAEs肾毒性最可能的调节机制。一致地,免疫荧光染色显示在高剂量CSAEs作用下,肾细胞和刷状缘中的F - 肌动蛋白和细胞骨架经常受到干扰。基因表达分析结果证实,CSAEs抑制了RhoA - ROCK信号通路中的关键蛋白,从而抑制了F - 肌动蛋白及其稳定基因的表达。总之,我们的研究结果表明,决明子可通过抑制RhoA - ROCK途径和/或直接与F - 肌动蛋白结合,使肌动蛋白细胞骨架解聚并使其不稳定,从而导致肾毒性。将决明子作为补充剂和药物食用值得关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1719/11360101/33e5a52db7e7/toxics-12-00556-g001.jpg

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