REACTION OF 4-HYDROXYNONENAL WITH SOME THIOL-CONTAINING RADIOPROTECTIVE AGENTS OR THEIR ACTIVE METABOLITES

Citation
Egd. Detoranzo et Ja. Castro, REACTION OF 4-HYDROXYNONENAL WITH SOME THIOL-CONTAINING RADIOPROTECTIVE AGENTS OR THEIR ACTIVE METABOLITES, Free radical biology & medicine, 17(6), 1994, pp. 605-607
Citations number
25
Categorie Soggetti
Biology
ISSN journal
08915849
Volume
17
Issue
6
Year of publication
1994
Pages
605 - 607
Database
ISI
SICI code
0891-5849(1994)17:6<605:RO4WST>2.0.ZU;2-2
Abstract
The rate of reaction of several radioprotective agents or their active metabolites with 4-hydroxynonenal (4HNE) was studied and compared to the rate of reaction with cysteine (Cys) and glutathione (GSH). The ag ents studied were: mercapto ethylamine (MEA); 2(3-aminopropyl) aminoet hanethiol (WR1065); S-2-aminoethylisothiouronium bromide-hydrobromide (AET); 1,4-dithiothreitol (DTT); 1,4-dithioerythritol (DTE); N 2(2-mer captopropionyl) -glycine (MPG); penicillamine hydro chloride (PA); N-a cetylcysteine (NAC); 2-3 dimercapto-1 propane sulfonic acid (DMPS); 2, 3-dimercaptopropanol (BAL), and meso 2,3 dimercapto succinic acid (DMS ). All of them reacted with 4HNE. MEA and WR1065 were the most reactiv e thiols, and PA and DMS were the least reactive thiols. All the other s reacted at rates comparable to or higher than that of cysteine or GS H. The potential role of this type of interactions in the protective a ction of these drugs against deleterious effects of radiation or carbo n tetrachloride is analyzed.