Pharmacological and dietary modulators of paraoxonase 1 (PON1) activity and expression: The hunt goes on

被引:140
作者
Costa, Lucio G. [1 ,4 ]
Giordano, Gennaro [1 ]
Furlong, Clement E. [2 ,3 ]
机构
[1] Univ Washington, Dept Environm & Occupat Hlth Sci, Seattle, WA 98105 USA
[2] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98105 USA
[3] Univ Washington, Dept Genome Sci, Seattle, WA 98105 USA
[4] Univ Parma, Sch Med, Dept Human Anat Pharmacol & Forens Sci, I-43100 Parma, Italy
基金
美国国家卫生研究院;
关键词
Paraoxonase; 1; Statins; Hypolipemic drugs; Anti-diabetic drugs; Antioxidants; Polyphenols; Alcohol; INCREASES SERUM PARAOXONASE; HIGH-DENSITY-LIPOPROTEIN; CHOLESTERYL ESTER TRANSFER; APOLIPOPROTEIN-A-I; E-DEFICIENT MICE; OXIDATIVE STRESS; GENE-EXPRESSION; PARAOXONASE/ARYLESTERASE ACTIVITIES; ANTIOXIDANT ENZYME; LIPID-PEROXIDATION;
D O I
10.1016/j.bcp.2010.11.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Paraoxonase 1 (PON1) is a high density lipoprotein (HDL)-associated enzyme displaying esterase and lactonase activity. PON1 hydrolyzes several organophosphorus (OP) insecticides and nerve agents, a number of exogenous and endogenous lactones, and metabolizes toxic oxidized lipids of low density lipoproteins (LDL) and HDL. As such, PON1 plays a relevant role in determining susceptibility to OP toxicity, cardiovascular diseases and several other diseases. Serum PON1 activity in a given population can vary by at least 40-fold. Most of this variation can be accounted for by genetic polymorphisms in the coding region (Q192R, L55M) and in the promoter region (T-108C). However, exogenous factors may also modulate PON1 activity and/or level of expression. This paper examines various factors that have been found to positively modulate PON1. Certain drugs (e.g. hypolipemic and anti-diabetic compounds), dietary factors (antioxidants, polyphenols), and life-style factors (moderate alcohol consumption) appear to increase PON1 activity. Given the relevance of PON1 in protecting from certain environmental exposure and from cardiovascular and other diseases, there is a need for further mechanistic, animal, and clinical research in this area, and for consideration of possible alternative strategies for increasing the levels and activity of PON1. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:337 / 344
页数:8
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