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
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.