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厚朴酚,一种多酚类天然化合物,通过细胞氧化应激和细胞骨架调节减轻顺铂诱导的肾上皮细胞急性细胞毒性。

Honokiol, a Polyphenol Natural Compound, Attenuates Cisplatin-Induced Acute Cytotoxicity in Renal Epithelial Cells Through Cellular Oxidative Stress and Cytoskeleton Modulations.

作者信息

Wang Tse-En J, Liu Hung-Ting, Lai Yu-Hua, Jan Tong-Rong, Nomura Naohiro, Chang Hui-Wen, Chou Chi-Chung, Lee Ya-Jane, Tsai Pei-Shiue J

机构信息

Department of Veterinary Medicine, School of Veterinary Medicine, National Taiwan University, Taipei, Taiwan.

Graduate Institute of Veterinary Medicine, School of Veterinary Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Front Pharmacol. 2018 Apr 24;9:357. doi: 10.3389/fphar.2018.00357. eCollection 2018.

DOI:10.3389/fphar.2018.00357
PMID:29755347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5932397/
Abstract

Cisplatin is a potent anti-cancer drug that has been widely used in the treatment of various cancers; however, cisplatin administration results in severe nephrotoxicity and impedes its clinical applications. In this study, we showed that honokiol, a polyphenol constituent extracted from exhibited a short-term protective effect against cisplatin-induced damages in renal epithelial cells . The protective effects of honokiol were resulted from the combination of (1) reduced cellular oxidative stress ranging from 53 to 32% reduction during a 24-h incubation, (2) the maintenance of cellular antioxidant capacity and (3) the stabilization of cytoskeletal structure of the kidney epithelial cells. By promoting the polymerization of actin (1.6-fold increase) and tubulin (1.8-fold increase) cytoskeleton, honokiol not only maintained epithelial cell morphology, but also stabilized cellular localizations of tight junction protein Occludin and adhesion junction protein E-Cadherin. With stabilized junction protein complexes and structural polymerized cytoskeleton network, honokiol preserved epithelial cell polarity and morphology and thus reduced cisplatin-induced cell disruption and damages. Our data demonstrated for the first time that honokiol could counteract with cisplatin-induced damages in renal epithelial cells , future studies would further validate the potential clinical application of honokiol in cisplatin-based cancer treatments with reduced nephrotoxicity.

摘要

顺铂是一种强效抗癌药物,已广泛用于各种癌症的治疗;然而,顺铂的使用会导致严重的肾毒性,阻碍其临床应用。在本研究中,我们表明厚朴酚(一种从[具体来源未给出]中提取的多酚成分)对顺铂诱导的肾上皮细胞损伤具有短期保护作用。厚朴酚的保护作用源于以下几个方面的结合:(1)在24小时孵育期间,细胞氧化应激降低,降低幅度从53%到32%不等;(2)细胞抗氧化能力的维持;(3)肾上皮细胞细胞骨架结构的稳定。通过促进肌动蛋白(增加1.6倍)和微管蛋白(增加1.8倍)细胞骨架的聚合,厚朴酚不仅维持了上皮细胞形态,还稳定了紧密连接蛋白闭合蛋白和黏附连接蛋白E-钙黏蛋白的细胞定位。由于连接蛋白复合物稳定且细胞骨架网络结构聚合,厚朴酚保留了上皮细胞极性和形态,从而减少了顺铂诱导的细胞破坏和损伤。我们的数据首次证明厚朴酚可以对抗顺铂诱导的肾上皮细胞损伤,未来的研究将进一步验证厚朴酚在基于顺铂的癌症治疗中降低肾毒性的潜在临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/4305a0ce67df/fphar-09-00357-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/16a823c0b55d/fphar-09-00357-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/ef844c3485b4/fphar-09-00357-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/f6b577e315cf/fphar-09-00357-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/4305a0ce67df/fphar-09-00357-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/7f9f2a13b4d7/fphar-09-00357-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/d7eb95ed40b3/fphar-09-00357-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/3d0311c10306/fphar-09-00357-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/436e9450a82d/fphar-09-00357-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/16a823c0b55d/fphar-09-00357-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/ef844c3485b4/fphar-09-00357-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/f6b577e315cf/fphar-09-00357-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa08/5932397/4305a0ce67df/fphar-09-00357-g008.jpg

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