Melatonin's antioxidant protection against δ-aminolevulinic acid-induced oxidative damage in rat cerebellum

δ-aminolevulinic acid (ALA) promotes the generation of reactive oxygen species (ROS). Accumulation of ALA, as occurs in acute intermittent porphyria (AIP), is a potential endogenous source of ROS, which can then exert oxidative damage to cell structures. In this work we investigated the role of phar...

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Autor principal: Princ, F.G
Otros Autores: Juknat, A.A, Maxit, A.G, Cardalda, C., Batlle, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Blackwell Publishing Ltd 1997
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024 7 |2 scopus  |a 2-s2.0-0031201899 
024 7 |2 cas  |a Aminolevulinic Acid, 106-60-5; Antioxidants; Malondialdehyde, 542-78-9; Melatonin, 73-31-4; Porphyrins; Reactive Oxygen Species 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JPRSE 
100 1 |a Princ, F.G. 
245 1 0 |a Melatonin's antioxidant protection against δ-aminolevulinic acid-induced oxidative damage in rat cerebellum 
260 |b Blackwell Publishing Ltd  |c 1997 
270 1 0 |m Batlle, A.Viamonte 1881-10o A, 1056 Buenos Aires, Argentina; email: cipyp@alad.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a δ-aminolevulinic acid (ALA) promotes the generation of reactive oxygen species (ROS). Accumulation of ALA, as occurs in acute intermittent porphyria (AIP), is a potential endogenous source of ROS, which can then exert oxidative damage to cell structures. In this work we investigated the role of pharmacological concentrations of melatonin on the deleterious effect of ALA and its effect on porphyrin biosynthesis. Rat cerebellum incubations were carried out with either ALA (1.0 mM) together with increasing concentrations of melatonin (0.1-2.0 mM) or 2.0 mM melatonin together with varying ALA concentrations (0.05-2.0 mM) for different times (1-4 hr). ALA-induced lipid peroxidation was significantly diminished by melatonin in a concentration-dependent manner. In all conditions 2.0 mM melatonin restored malondialdehyde levels to control values. In incubations without ALA, melatonin markedly reduced (36-40%) the basal levels of lipid peroxidation when compared with the corresponding controls. ALA uptake and porphyrin accumulation were increased 30% in incubations with 1.0-2.0 mM ALA for 4 hr in the presence of 2.0 mM melatonin, providing evidence for the involvement of ALA-promoted ROS in the damage of enzymes related to porphyrin biosynthesis. These results are further support for the protective role of melatonin against oxidative damage induced by ALA; this protective action of melatonin is probably due to melatonin's antioxidant and free radical scavenger properties. The development of a new therapeutic approach for AIP patients employing melatonin alone or in combination with conventional treatments should be considered.  |l eng 
593 |a Ctro. Invest. sobre Porfirinas y P., Depto. de Quim. Biológica, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina 
593 |a Viamonte 1881-10o A, 1056 Buenos Aires, Argentina 
690 1 0 |a MELATONIN 
690 1 0 |a PORPHYRINOGENESIS 
690 1 0 |a RAT CEREBELLUM 
690 1 0 |a REACTIVE OXYGEN SPECIES 
690 1 0 |a Δ-AMINOLEVULINIC ACID 
690 1 0 |a AMINOLEVULINIC ACID 
690 1 0 |a ANTIOXIDANT 
690 1 0 |a MALONALDEHYDE 
690 1 0 |a MELATONIN 
690 1 0 |a PORPHYRIN 
690 1 0 |a REACTIVE OXYGEN METABOLITE 
690 1 0 |a ANIMAL 
690 1 0 |a ARTICLE 
690 1 0 |a CEREBELLUM 
690 1 0 |a DRUG EFFECT 
690 1 0 |a LIPID PEROXIDATION 
690 1 0 |a MALE 
690 1 0 |a METABOLISM 
690 1 0 |a RAT 
690 1 0 |a AMINOLEVULINIC ACID 
690 1 0 |a ANIMALS 
690 1 0 |a ANTIOXIDANTS 
690 1 0 |a CEREBELLUM 
690 1 0 |a LIPID PEROXIDATION 
690 1 0 |a MALE 
690 1 0 |a MALONDIALDEHYDE 
690 1 0 |a MELATONIN 
690 1 0 |a PORPHYRINS 
690 1 0 |a RATS 
690 1 0 |a REACTIVE OXYGEN SPECIES 
700 1 |a Juknat, A.A. 
700 1 |a Maxit, A.G. 
700 1 |a Cardalda, C. 
700 1 |a Batlle, A. 
773 0 |d Blackwell Publishing Ltd, 1997  |g v. 23  |h pp. 40-46  |k n. 1  |p J. Pineal Res.  |x 07423098  |t Journal of Pineal Research 
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