z-logo
Premium
Resveratrol induces catalytic bioscavenger paraoxonase 1 expression and protects against chemical warfare nerve agent toxicity in human cell lines
Author(s) -
Curtin Bryan F.,
Seetharam Karthik I.,
Dhoieam Pilin,
Gordon Richard K.,
Doctor Bhupendra P.,
Nambiar Madhusoodana P.
Publication year - 2007
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.21543
Subject(s) - nerve agent , sarin , toxicity , soman , chemistry , pharmacology , organophosphate , resveratrol , butyrylcholinesterase , viability assay , paraoxonase , apoptosis , biochemistry , enzyme , acetylcholinesterase , biology , aché , organic chemistry , pesticide , agronomy
Current advances in enzyme bioscavenger prophylactic therapy against chemical warfare nerve agent (CWNA) exposure are moving towards the identification of catalytic bioscavengers that can degrade large doses of organophosphate (OP) nerve agents without self destruction. This is a preferred method compared to therapy with the purified stoichiometric bioscavenger, butyrylcholinesterase, which binds OPs 1:1 and would thus require larger doses for treatment. Paraoxonase‐1 (PON‐1) is one such catalytic bioscavenger that has been shown to hydrolyze OP insecticides and contribute to detoxification in animals and humans. Here we investigated the effects of a common red wine ingredient, Resveratrol (RSV), to induce the expression of PON‐1 in the human hepatic cell line HC04 and evaluated the protection against CWNA simulants. Dose‐response curves showed that a concentration of 20 µM RSV was optimal in inducing PON‐1 expression in HC04 cells. RSV at 20 µM increased the extracellular PON‐1 activity approximately 150% without significantly affecting the cells. Higher doses of RSV were cytotoxic to the cells. Resveratrol also induced PON‐1 in the human lung cell line A549. RSV pre‐treatment significantly ( P  = 0.05) protected the hepatic cells against exposure to 2× LD 50 of soman and sarin simulants. However, lung cells were protected against soman simulant exposure but not against sarin simulant exposure following RSV treatment. In conclusion, these studies indicate that dietary inducers, such as RSV, can up‐regulate PON‐1, a catalytic bioscavenger, which can then hydrolyze and protect against CWNA‐induced toxicity, providing a prospective new method to protect against CWNA exposure. J. Cell. Biochem. 103: 1524–1535, 2008. © 2007 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here