Tryptophan metabolism via serotonin in rats with hexachlorobenzene experimental porphyria
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 meta...
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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 |
_version_ |
1768543683390472192 |