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迷迭香酸及其主要代谢产物在化学和细胞体系中的抗氧化活性:物理化学特性的重要性

Antioxidant activity of rosmarinic acid and its principal metabolites in chemical and cellular systems: Importance of physico-chemical characteristics.

作者信息

Adomako-Bonsu Amma G, Chan Sue Lf, Pratten Margaret, Fry Jeffrey R

机构信息

School of Life Sciences, University of Nottingham, Queen's Medical Centre, Nottingham NG7 2UH, UK.

School of Life Sciences, University of Nottingham, Queen's Medical Centre, Nottingham NG7 2UH, UK.

出版信息

Toxicol In Vitro. 2017 Apr;40:248-255. doi: 10.1016/j.tiv.2017.01.016. Epub 2017 Jan 22.

Abstract

Persistent accumulation of reactive oxygen species causes cellular oxidative stress which contributes strongly towards the induction and progression of various diseases. Therapeutic focus has therefore shifted towards the use of antioxidants, with recent interest in those of plant origin. In the current study, rosmarinic acid (RA) and its key metabolites were evaluated in non-cellular and cellular antioxidant assays, using quercetin (Q) as a positive control. The non-cellular assay was performed as scavenging of DPPH radical, whilst the cellular assay was performed as protection from an oxidant stress. Radical-scavenging activity of RA and two of its primary metabolites, CA and DHPLA, were comparable to that of Q, whilst FA was of lower potency and m-CoA was inactive. In the cellular assay, RA and CA were markedly less potent than Q, with DHPLA, FA and m-CoA being inactive, this being true in short-term (5-h) or long-term (20-h) exposure conditions. However, antioxidant potency of Q and methyl rosmarinate, a non-ionisable ester of RA, was similar in the non-cellular and short-term cellular assays. It is proposed that marked ionisation of organic acids such as RA and its metabolites at physiological pH greatly limits their intracellular accumulation, and so attenuates intrinsic antioxidant ability demonstrated in the non-cellular assay. This study demonstrates some of the factors that prevent well-known phytochemicals from progressing further along the drug discovery chain.

摘要

活性氧的持续积累会导致细胞氧化应激,这在很大程度上促进了各种疾病的诱发和发展。因此,治疗重点已转向使用抗氧化剂,最近对植物源抗氧化剂产生了兴趣。在本研究中,以槲皮素(Q)作为阳性对照,在非细胞和细胞抗氧化试验中评估了迷迭香酸(RA)及其关键代谢产物。非细胞试验以清除DPPH自由基的方式进行,而细胞试验以抵御氧化应激的方式进行。RA及其两种主要代谢产物咖啡酸(CA)和二氢迷迭香酸(DHPLA)的自由基清除活性与Q相当,而迷迭香酸乙酯(FA)的效力较低,甲基辅酶A(m-CoA)无活性。在细胞试验中,RA和CA的效力明显低于Q,DHPLA、FA和m-CoA无活性,在短期(5小时)或长期(20小时)暴露条件下均如此。然而,在非细胞和短期细胞试验中,Q和RA的非离子化酯甲基迷迭香酸的抗氧化效力相似。有人提出,RA及其代谢产物等有机酸在生理pH值下的显著离子化极大地限制了它们在细胞内的积累,从而削弱了非细胞试验中显示的内在抗氧化能力。这项研究揭示了一些阻碍著名植物化学物质在药物研发链上进一步发展的因素。

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