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

被引:146
作者
Adomako-Bonsu, Amma G. [1 ]
Chan, Sue L. F. [1 ]
Pratten, Margaret [1 ]
Fry, Jeffrey R. [1 ]
机构
[1] Univ Nottingham, Queens Med Ctr, Sch Life Sci, Nottingham NG7 2UH, England
关键词
Rosmarinic acid; Metabolites; Quercetin; Cytoprotection; HepG2; cells; Oxidative stress; BAMBANGAN MANGIFERA-PAJANG; IN-VITRO; PHENOLIC-COMPOUNDS; SERUM; POLYPHENOLS; EXTRACT; HEPG2; PHYTOCHEMICALS; CYTOTOXICITY; CELLS;
D O I
10.1016/j.tiv.2017.01.016
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
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 in-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. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:248 / 255
页数:8
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