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Role of taurine on acid secretion in the rat stomach

BACKGROUND: Taurine has chemical structure similar to an inhibitory neurotransmitter, γ-aminobutyric acid (GABA). Previous studies on GABA in the stomach suggest GABAergic neuron is involved in acid secretion, but the effects of taurine are poor understood. METHODS: The effects of taurine on acid se...

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Autores principales: Huang, Kai-Han, Chang, Chia-Chieh, Ho, Jau-Der, Lu, Ruey-Hwa, Tsai, Li Hsueh
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042912/
https://www.ncbi.nlm.nih.gov/pubmed/21294907
http://dx.doi.org/10.1186/1423-0127-18-11
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author Huang, Kai-Han
Chang, Chia-Chieh
Ho, Jau-Der
Lu, Ruey-Hwa
Tsai, Li Hsueh
author_facet Huang, Kai-Han
Chang, Chia-Chieh
Ho, Jau-Der
Lu, Ruey-Hwa
Tsai, Li Hsueh
author_sort Huang, Kai-Han
collection PubMed
description BACKGROUND: Taurine has chemical structure similar to an inhibitory neurotransmitter, γ-aminobutyric acid (GABA). Previous studies on GABA in the stomach suggest GABAergic neuron is involved in acid secretion, but the effects of taurine are poor understood. METHODS: The effects of taurine on acid secretion, signal transduction, and localization of taurinergic neurons were determined in the rat stomach using everted whole stomach, RIA kit and immunohistochemical methods. RESULTS: We used antibodies against taurine-synthesizing enzyme, cysteine sulfuric acid decarboxylase (CSAD), and taurine. CSAD- and taurine-positive cells were found in the muscle and mucosal layers. Distributions of CSAD- and taurine-positive cells in both mucosal and muscle layers were heterogeneous in the stomach. Taurine at 10(-9)~10(-4 )M induced acid secretion, and the maximum secretion was at 10(-5 )M, 1.6-fold higher than the spontaneous secretion. Taurine-induced acid secretion was completely inhibited by bicuculline and atropine but not by cimetidine, proglumide, or strychnine. Atropine and tetrodotoxin (TTX) completely inhibited the acid secretion induced by low concentrations of taurine and partially inhibited induced by high concentrations. Verapamil, a calcium blocker agent, inhibited acid output elicited by taurine. We assumed all Ca(2+ )channels involved in the response to these secretagogues were equally affected by verapamil. Intracellular cAMP (adenosine 3', 5'-monophosphat) in the stomach significantly increased with taurine treatment in a dose-dependent manner. High correlation (r=0.859, p < 0.001) of taurine concentrations with cAMP was observed. CONCLUSIONS: Our results demonstrated for the first time in taurine-induced acid secretion due to increase intracellular calcium may act through the A type of GABA receptors, which are mainly located on cholinergic neurons though cAMP pathway and partially on nonneuronal cells in the rat stomach.
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spelling pubmed-30429122011-02-23 Role of taurine on acid secretion in the rat stomach Huang, Kai-Han Chang, Chia-Chieh Ho, Jau-Der Lu, Ruey-Hwa Tsai, Li Hsueh J Biomed Sci Research BACKGROUND: Taurine has chemical structure similar to an inhibitory neurotransmitter, γ-aminobutyric acid (GABA). Previous studies on GABA in the stomach suggest GABAergic neuron is involved in acid secretion, but the effects of taurine are poor understood. METHODS: The effects of taurine on acid secretion, signal transduction, and localization of taurinergic neurons were determined in the rat stomach using everted whole stomach, RIA kit and immunohistochemical methods. RESULTS: We used antibodies against taurine-synthesizing enzyme, cysteine sulfuric acid decarboxylase (CSAD), and taurine. CSAD- and taurine-positive cells were found in the muscle and mucosal layers. Distributions of CSAD- and taurine-positive cells in both mucosal and muscle layers were heterogeneous in the stomach. Taurine at 10(-9)~10(-4 )M induced acid secretion, and the maximum secretion was at 10(-5 )M, 1.6-fold higher than the spontaneous secretion. Taurine-induced acid secretion was completely inhibited by bicuculline and atropine but not by cimetidine, proglumide, or strychnine. Atropine and tetrodotoxin (TTX) completely inhibited the acid secretion induced by low concentrations of taurine and partially inhibited induced by high concentrations. Verapamil, a calcium blocker agent, inhibited acid output elicited by taurine. We assumed all Ca(2+ )channels involved in the response to these secretagogues were equally affected by verapamil. Intracellular cAMP (adenosine 3', 5'-monophosphat) in the stomach significantly increased with taurine treatment in a dose-dependent manner. High correlation (r=0.859, p < 0.001) of taurine concentrations with cAMP was observed. CONCLUSIONS: Our results demonstrated for the first time in taurine-induced acid secretion due to increase intracellular calcium may act through the A type of GABA receptors, which are mainly located on cholinergic neurons though cAMP pathway and partially on nonneuronal cells in the rat stomach. BioMed Central 2011-02-05 /pmc/articles/PMC3042912/ /pubmed/21294907 http://dx.doi.org/10.1186/1423-0127-18-11 Text en Copyright ©2011 Huang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Huang, Kai-Han
Chang, Chia-Chieh
Ho, Jau-Der
Lu, Ruey-Hwa
Tsai, Li Hsueh
Role of taurine on acid secretion in the rat stomach
title Role of taurine on acid secretion in the rat stomach
title_full Role of taurine on acid secretion in the rat stomach
title_fullStr Role of taurine on acid secretion in the rat stomach
title_full_unstemmed Role of taurine on acid secretion in the rat stomach
title_short Role of taurine on acid secretion in the rat stomach
title_sort role of taurine on acid secretion in the rat stomach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042912/
https://www.ncbi.nlm.nih.gov/pubmed/21294907
http://dx.doi.org/10.1186/1423-0127-18-11
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