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spelling todo:paper_10915818_v26_n6_p545_Llambias2023-10-03T16:04:57Z Melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria Llambías, E.B.C. Mazzetti, M.B. Lelli, S.M. Aldonatti, C. De Viale, L.C.S.M. Experimental Hepatic Porphyria Hexachlorobenzene Melatonin Porphyria Cutanea Tarda Tryptophan Tryptophan Metabolites 5 hydroxyindoleacetic acid acetylserotonin methyltransferase hexachlorobenzene melatonin serotonin tryptophan animal experiment animal model animal tissue article controlled study enzyme activity female hyperpigmentation nonhuman oxidative stress pineal body porphyria cutanea tarda rat Acetylserotonin O-Methyltransferase Animals Circadian Rhythm Disease Models, Animal Female Hexachlorobenzene Hydroxyindoleacetic Acid Light Melatonin Pineal Gland Porphyria Cutanea Tarda Rats Rats, Wistar Serotonin Tryptophan Tryptophan Hydroxylase Animalia Rattus Hexachlorobenzene produces an experimental hepatic porphyria in rats, which is similar to human porphyria cutanea tarda, with hyperpigmentation as one of its characteristic features. Alterations in tryptophan metabolism have been previously observed in this chronic porphyria. Melatonin formation from tryptophan via serotonin shows diurnal rhythmicity in the pineal gland, and higher values are observed during the dark phase of an imposed light-dark cycle. The purpose of this study was to determine the contents of tryptophan and its metabolites in pineal gland of normal and hexachlorobenzene-treated rats in order to find alterations potentially related to porphyria cutanea tarda. Results show that in animals with this experimental porphyria some tryptophan metabolite levels (serotonin and 5-hydroxyindoleacetic acid) increase only during the light period, whereas tryptophan content remained equal to the controls. Hydroxyindole-O-methyltransferase activity also increases by light in pineal gland from hexachlorobenzene-treated rats. On the other hand, tryptophan is converted to melatonin in the dark period, but this route is not exacerbated in hexachlorobenzene porphyria. The relevance of these alterations is discussed in relation to hyperpigmentation, neoplastic and oxidative stress processes associated with this porphyria. Copyright © American College of Toxicology. Fil:Llambías, E.B.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Mazzetti, M.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Lelli, S.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_10915818_v26_n6_p545_Llambias
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Experimental Hepatic Porphyria
Hexachlorobenzene
Melatonin
Porphyria Cutanea Tarda
Tryptophan
Tryptophan Metabolites
5 hydroxyindoleacetic acid
acetylserotonin methyltransferase
hexachlorobenzene
melatonin
serotonin
tryptophan
animal experiment
animal model
animal tissue
article
controlled study
enzyme activity
female
hyperpigmentation
nonhuman
oxidative stress
pineal body
porphyria cutanea tarda
rat
Acetylserotonin O-Methyltransferase
Animals
Circadian Rhythm
Disease Models, Animal
Female
Hexachlorobenzene
Hydroxyindoleacetic Acid
Light
Melatonin
Pineal Gland
Porphyria Cutanea Tarda
Rats
Rats, Wistar
Serotonin
Tryptophan
Tryptophan Hydroxylase
Animalia
Rattus
spellingShingle Experimental Hepatic Porphyria
Hexachlorobenzene
Melatonin
Porphyria Cutanea Tarda
Tryptophan
Tryptophan Metabolites
5 hydroxyindoleacetic acid
acetylserotonin methyltransferase
hexachlorobenzene
melatonin
serotonin
tryptophan
animal experiment
animal model
animal tissue
article
controlled study
enzyme activity
female
hyperpigmentation
nonhuman
oxidative stress
pineal body
porphyria cutanea tarda
rat
Acetylserotonin O-Methyltransferase
Animals
Circadian Rhythm
Disease Models, Animal
Female
Hexachlorobenzene
Hydroxyindoleacetic Acid
Light
Melatonin
Pineal Gland
Porphyria Cutanea Tarda
Rats
Rats, Wistar
Serotonin
Tryptophan
Tryptophan Hydroxylase
Animalia
Rattus
Llambías, E.B.C.
Mazzetti, M.B.
Lelli, S.M.
Aldonatti, C.
De Viale, L.C.S.M.
Melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria
topic_facet Experimental Hepatic Porphyria
Hexachlorobenzene
Melatonin
Porphyria Cutanea Tarda
Tryptophan
Tryptophan Metabolites
5 hydroxyindoleacetic acid
acetylserotonin methyltransferase
hexachlorobenzene
melatonin
serotonin
tryptophan
animal experiment
animal model
animal tissue
article
controlled study
enzyme activity
female
hyperpigmentation
nonhuman
oxidative stress
pineal body
porphyria cutanea tarda
rat
Acetylserotonin O-Methyltransferase
Animals
Circadian Rhythm
Disease Models, Animal
Female
Hexachlorobenzene
Hydroxyindoleacetic Acid
Light
Melatonin
Pineal Gland
Porphyria Cutanea Tarda
Rats
Rats, Wistar
Serotonin
Tryptophan
Tryptophan Hydroxylase
Animalia
Rattus
description Hexachlorobenzene produces an experimental hepatic porphyria in rats, which is similar to human porphyria cutanea tarda, with hyperpigmentation as one of its characteristic features. Alterations in tryptophan metabolism have been previously observed in this chronic porphyria. Melatonin formation from tryptophan via serotonin shows diurnal rhythmicity in the pineal gland, and higher values are observed during the dark phase of an imposed light-dark cycle. The purpose of this study was to determine the contents of tryptophan and its metabolites in pineal gland of normal and hexachlorobenzene-treated rats in order to find alterations potentially related to porphyria cutanea tarda. Results show that in animals with this experimental porphyria some tryptophan metabolite levels (serotonin and 5-hydroxyindoleacetic acid) increase only during the light period, whereas tryptophan content remained equal to the controls. Hydroxyindole-O-methyltransferase activity also increases by light in pineal gland from hexachlorobenzene-treated rats. On the other hand, tryptophan is converted to melatonin in the dark period, but this route is not exacerbated in hexachlorobenzene porphyria. The relevance of these alterations is discussed in relation to hyperpigmentation, neoplastic and oxidative stress processes associated with this porphyria. Copyright © American College of Toxicology.
format JOUR
author Llambías, E.B.C.
Mazzetti, M.B.
Lelli, S.M.
Aldonatti, C.
De Viale, L.C.S.M.
author_facet Llambías, E.B.C.
Mazzetti, M.B.
Lelli, S.M.
Aldonatti, C.
De Viale, L.C.S.M.
author_sort Llambías, E.B.C.
title Melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria
title_short Melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria
title_full Melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria
title_fullStr Melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria
title_full_unstemmed Melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria
title_sort melatonin formation in pineal gland from rats with hexachlorobenzene experimental porphyria
url http://hdl.handle.net/20.500.12110/paper_10915818_v26_n6_p545_Llambias
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