Abstract
Oxidative stress (OS) is thought to play an important role in the pharmacological and toxic effects of various drugs of abuse. Herein we review the literature on the mechanisms responsible for the cardiovascular and hepatic toxicity of cocaine with special focus on OS-related mechanisms. We also review the preclinical and clinical literature concerning the putative therapeutic effects of OS modulators (such as N-acetylcysteine, superoxide dismutase mimetics, nitroxides and nitrones, NADPH oxidase inhibitors, xanthine oxidase inhibitors, and mitochondriotropic antioxidants) for the treatment of cocaine toxicity. We conclude that available OS modulators do not appear to have clinical efficacy.
MeSH terms
-
Acetylcysteine / chemistry
-
Animals
-
Antioxidants / pharmacology
-
Cardiovascular Diseases / chemically induced*
-
Catecholamines / metabolism
-
Cattle
-
Cocaine / chemistry*
-
Cocaine / toxicity*
-
Humans
-
Liver / drug effects*
-
Male
-
Mice
-
Mitochondria / drug effects
-
Myocytes, Smooth Muscle / metabolism
-
NADPH Oxidases / antagonists & inhibitors
-
Nitrogen Oxides / chemistry
-
Oxidative Stress*
-
Rats
-
Reactive Oxygen Species / metabolism
-
Receptors, Adrenergic, alpha-1 / metabolism
-
Receptors, Adrenergic, beta / metabolism
-
Xanthine Oxidase / antagonists & inhibitors
Substances
-
Antioxidants
-
Catecholamines
-
Nitrogen Oxides
-
Reactive Oxygen Species
-
Receptors, Adrenergic, alpha-1
-
Receptors, Adrenergic, beta
-
nitrones
-
Xanthine Oxidase
-
NADPH Oxidases
-
Cocaine
-
Acetylcysteine