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姜黄提取物通过降低 BV2 小胶质细胞中一氧化氮、iNOS 蛋白和 mRNA 合成来发挥抗氧化作用。

Turmeric Extract () Mediates Anti-Oxidative Effects by Reduction of Nitric Oxide, iNOS Protein-, and mRNA-Synthesis in BV2 Microglial Cells.

机构信息

Neuroimmunology and Neurochemistry Research Group, Department of Psychiatry and Psychotherapy, Medical Center, University of Freiburg, D-79104 Freiburg, Germany.

Faculty of Medicine, University of Freiburg, D-79104 Freiburg, Germany.

出版信息

Molecules. 2022 Jan 25;27(3):784. doi: 10.3390/molecules27030784.

Abstract

Plant-derived products have been used since the beginnings of human history to treat various pathological conditions. Practical experience as well as a growing body of research suggests the benefits of the use of turmeric () and some of its active components in the reduction of oxidative stress, a mechanism leading to neurodegeneration. In this current study, we investigated the effects of a preparation of , and its constituents curcumin, tetrahydrocurcumin, and curcumenol, in one of the molecular pathways leading to oxidative stress, which is the release of NO, a free radical involved in stress conditions, using the BV2 microglial cell line. The concentration-dependent reduction of NO is linked to reduced amounts of iNOS protein- and mRNA-synthesis and is possibly mediated by the phosphorylation of mitogen-activated protein kinases (MAPK) such as p42/44 or p38 MAPK. Therefore, the use of turmeric extract is a promising therapeutic option for diseases linked to the dysregulation of oxidative stress, with fewer side-effects in comparison to the currently used pharmacotherapeutics.

摘要

植物衍生产品自人类历史之初就被用于治疗各种病理状况。实践经验和越来越多的研究表明,使用姜黄()及其一些活性成分来减轻氧化应激的益处,氧化应激是导致神经退行性变的一种机制。在本研究中,我们使用 BV2 小胶质细胞系研究了姜黄制剂及其成分姜黄素、四氢姜黄素和莪术醇在导致氧化应激的分子途径之一中(即自由基 NO 的释放)的作用,NO 是一种与应激条件有关的自由基。NO 的浓度依赖性减少与 iNOS 蛋白和 mRNA 合成量的减少有关,并且可能通过丝裂原活化蛋白激酶(MAPK)如 p42/44 或 p38 MAPK 的磷酸化来介导。因此,与目前使用的药物治疗相比,使用姜黄提取物是治疗与氧化应激失调相关疾病的一种有前途的治疗选择,副作用更少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/8840760/cc9e592470f0/molecules-27-00784-g001.jpg

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