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δ‐Aminolevulinic acid‐induced lipid peroxidation in rat kidney and liver is attenuated by melatonin: An in vitro and in vivo study
Author(s) -
Carneiro Regina C.G.,
Reiter Russel J.
Publication year - 1998
Publication title -
journal of pineal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 131
eISSN - 1600-079X
pISSN - 0742-3098
DOI - 10.1111/j.1600-079x.1998.tb00524.x
Subject(s) - melatonin , lipid peroxidation , in vivo , kidney , toxicity , chemistry , endocrinology , pharmacology , medicine , biochemistry , biology , oxidative stress , microbiology and biotechnology
Acute intermittent porphyria (AIP) is a genetically inherited disease characterized by a partial block in liver heme biosynthesis and by increased urinary excretion of the δ‐aminolevulinic acid (ALA). Recently, it has been proposed that the toxic effects of ALA are related to the generation of free radicals. In the present study the in vitro and in vivo effect of melatonin, a recently described antioxidative agent, on ALA‐induced lipid peroxidation in rat liver and kidney was determined. The concentration of malonaldehyde (MDA) and 4‐hydroxyalkenals (4‐HDA) was assayed as an index of induced membrane oxidative damage. In vitro melatonin protected, in a concentration‐dependent manner, against ALA‐induced lipid peroxidation in liver and kidney homogenates. In in vivo experiments as well, it was demonstrated that ALA (40 mg/kg)‐induced lipid peroxidation in liver and kidney was reduced by acute melatonin (10 m/g) treatment. The results support the involvement of free radicals in ALA toxicity and show that in vitro and in vivo melatonin confers protection against this toxicity, likely due to the antioxidative capability of the indole.