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spelling paper:paper_00062952_v66_n1_p35_Llambias2023-06-08T14:30:34Z Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria Llambías, Elena Blanca Cecilia San Martín de Viale, Leonor Carmen Experimental hepatic porphyria Hexachlorobenzene Metabolites of tryptophan pathway via serotonin Porphyria Cutanea Tarda Tryptophan Tryptophan hydroxylase 5 hydroxyindoleacetic acid 5 hydroxytryptophan hexachlorobenzene serotonin tryptophan tryptophan hydroxylase amino acid blood level amino acid urine level animal experiment animal model animal tissue article controlled study enzyme activity female high performance liquid chromatography nonhuman porphyria cutanea tarda priority journal protein metabolism rat regulatory mechanism tissue level tryptophan brain level tryptophan metabolism urinary excretion One of the three pathways for the metabolisation of dietary tryptophan is the formation of serotonin. Tryptophan hydroxylase catalyses the formation of 5-hydroxytryptophan, the first and regulatory step of this biosynthesis. The aim of the present work is to study alterations in this tryptophan metabolism in rats with experimental Porphyria Cutanea Tarda induced by hexachlorobenzene. With this purpose, the content of tryptophan and its metabolites related to the serotonin pathway are determined by HPLC techniques, in tissues (brain, liver and gut) and in fluids (blood, plasma and urine) of controls and hexachlorobenzene-porphyric rats. In these experimental-porphyric animals, we determine a significant increase in the excretion of 5-hydroxyindole acetic acid in urine and a decrease in the content of serotonin in small gut, respect to controls. Significant increases in contents of serotonin in 24-hr urine and tryptophan in liver are also found. No other significant variations for the different metabolites are detected in any of the tissues and fluids studied. Brain and liver activities of the rate-limiting enzyme tryptophan hydroxylase can only be measured in porphyric rats. Our results agree with an increased turnover of gastrointestinal serotonin derived from dietary tryptophan and its excretion as urinary 5-hydroxyindole acetic acid, which is formed in liver. An increased serotonin pathway in porphyric livers is confirmed by the measured increase in the activity of hepatic tryptophan hydroxylase. The absence of neurological symptoms in patients with Porphyria Cutanea Tarda could be related to the absence of a statistically significant variation in serotonin content shown in brain. © 2003 Elsevier Science Inc. All rights reserved. Fil:Llambías, E.B.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:San Martín De Viale, L.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2003 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00062952_v66_n1_p35_Llambias http://hdl.handle.net/20.500.12110/paper_00062952_v66_n1_p35_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
Metabolites of tryptophan pathway via serotonin
Porphyria Cutanea Tarda
Tryptophan
Tryptophan hydroxylase
5 hydroxyindoleacetic acid
5 hydroxytryptophan
hexachlorobenzene
serotonin
tryptophan
tryptophan hydroxylase
amino acid blood level
amino acid urine level
animal experiment
animal model
animal tissue
article
controlled study
enzyme activity
female
high performance liquid chromatography
nonhuman
porphyria cutanea tarda
priority journal
protein metabolism
rat
regulatory mechanism
tissue level
tryptophan brain level
tryptophan metabolism
urinary excretion
spellingShingle Experimental hepatic porphyria
Hexachlorobenzene
Metabolites of tryptophan pathway via serotonin
Porphyria Cutanea Tarda
Tryptophan
Tryptophan hydroxylase
5 hydroxyindoleacetic acid
5 hydroxytryptophan
hexachlorobenzene
serotonin
tryptophan
tryptophan hydroxylase
amino acid blood level
amino acid urine level
animal experiment
animal model
animal tissue
article
controlled study
enzyme activity
female
high performance liquid chromatography
nonhuman
porphyria cutanea tarda
priority journal
protein metabolism
rat
regulatory mechanism
tissue level
tryptophan brain level
tryptophan metabolism
urinary excretion
Llambías, Elena Blanca Cecilia
San Martín de Viale, Leonor Carmen
Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
topic_facet Experimental hepatic porphyria
Hexachlorobenzene
Metabolites of tryptophan pathway via serotonin
Porphyria Cutanea Tarda
Tryptophan
Tryptophan hydroxylase
5 hydroxyindoleacetic acid
5 hydroxytryptophan
hexachlorobenzene
serotonin
tryptophan
tryptophan hydroxylase
amino acid blood level
amino acid urine level
animal experiment
animal model
animal tissue
article
controlled study
enzyme activity
female
high performance liquid chromatography
nonhuman
porphyria cutanea tarda
priority journal
protein metabolism
rat
regulatory mechanism
tissue level
tryptophan brain level
tryptophan metabolism
urinary excretion
description One of the three pathways for the metabolisation of dietary tryptophan is the formation of serotonin. Tryptophan hydroxylase catalyses the formation of 5-hydroxytryptophan, the first and regulatory step of this biosynthesis. The aim of the present work is to study alterations in this tryptophan metabolism in rats with experimental Porphyria Cutanea Tarda induced by hexachlorobenzene. With this purpose, the content of tryptophan and its metabolites related to the serotonin pathway are determined by HPLC techniques, in tissues (brain, liver and gut) and in fluids (blood, plasma and urine) of controls and hexachlorobenzene-porphyric rats. In these experimental-porphyric animals, we determine a significant increase in the excretion of 5-hydroxyindole acetic acid in urine and a decrease in the content of serotonin in small gut, respect to controls. Significant increases in contents of serotonin in 24-hr urine and tryptophan in liver are also found. No other significant variations for the different metabolites are detected in any of the tissues and fluids studied. Brain and liver activities of the rate-limiting enzyme tryptophan hydroxylase can only be measured in porphyric rats. Our results agree with an increased turnover of gastrointestinal serotonin derived from dietary tryptophan and its excretion as urinary 5-hydroxyindole acetic acid, which is formed in liver. An increased serotonin pathway in porphyric livers is confirmed by the measured increase in the activity of hepatic tryptophan hydroxylase. The absence of neurological symptoms in patients with Porphyria Cutanea Tarda could be related to the absence of a statistically significant variation in serotonin content shown in brain. © 2003 Elsevier Science Inc. All rights reserved.
author Llambías, Elena Blanca Cecilia
San Martín de Viale, Leonor Carmen
author_facet Llambías, Elena Blanca Cecilia
San Martín de Viale, Leonor Carmen
author_sort Llambías, Elena Blanca Cecilia
title Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
title_short Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
title_full Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
title_fullStr Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
title_full_unstemmed Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
title_sort tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
publishDate 2003
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00062952_v66_n1_p35_Llambias
http://hdl.handle.net/20.500.12110/paper_00062952_v66_n1_p35_Llambias
work_keys_str_mv AT llambiaselenablancacecilia tryptophanmetabolismviaserotonininratswithhexachlorobenzeneexperimentalporphyria
AT sanmartindevialeleonorcarmen tryptophanmetabolismviaserotonininratswithhexachlorobenzeneexperimentalporphyria
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