Modulatory effects of taurine on jejunal contractility

Taurine (2-aminoethanesulfonic acid) is widely distributed in animal tissues and has diverse pharmacological effects. However, the role of taurine in modulating smooth muscle contractility is still controversial. We propose that taurine (5-80 mM) can exert bidirectional modulation on the contractili...

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Main Authors: Q.Y. Yao, D.P. Chen, D.M. Ye, Y.P. Diao, Y. Lin
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2014-12-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2014001201068&lng=en&tlng=en
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author Q.Y. Yao
D.P. Chen
D.M. Ye
Y.P. Diao
Y. Lin
author_facet Q.Y. Yao
D.P. Chen
D.M. Ye
Y.P. Diao
Y. Lin
author_sort Q.Y. Yao
collection DOAJ
description Taurine (2-aminoethanesulfonic acid) is widely distributed in animal tissues and has diverse pharmacological effects. However, the role of taurine in modulating smooth muscle contractility is still controversial. We propose that taurine (5-80 mM) can exert bidirectional modulation on the contractility of isolated rat jejunal segments. Different low and high contractile states were induced in isolated jejunal segments of rats to observe the effects of taurine and the associated mechanisms. Taurine induced stimulatory effects on the contractility of isolated rat jejunal segments at 3 different low contractile states, and inhibitory effects at 3 different high contractile states. Bidirectional modulation was not observed in the presence of verapamil or tetrodotoxin, suggesting that taurine-induced bidirectional modulation is Ca2+ dependent and requires the presence of the enteric nervous system. The stimulatory effects of taurine on the contractility of isolated jejunal segments was blocked by atropine but not by diphenhydramine or by cimetidine, suggesting that muscarinic-linked activation was involved in the stimulatory effects when isolated jejunal segments were in a low contractile state. The inhibitory effects of taurine on the contractility of isolated jejunal segments were blocked by propranolol and L-NG-nitroarginine but not by phentolamine, suggesting that adrenergic β receptors and a nitric oxide relaxing mechanism were involved when isolated jejunal segments were in high contractile states. No bidirectional effects of taurine on myosin phosphorylation were observed. The contractile states of jejunal segments determine taurine-induced stimulatory or inhibitory effects, which are associated with muscarinic receptors and adrenergic β receptors, and a nitric oxide associated relaxing mechanism.
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spelling doaj.art-1a587121aa744e8394582ba4385d02bf2022-12-21T23:34:38ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2014-12-0147121068107410.1590/1414-431X20142890S0100-879X2014001201068Modulatory effects of taurine on jejunal contractilityQ.Y. YaoD.P. ChenD.M. YeY.P. DiaoY. LinTaurine (2-aminoethanesulfonic acid) is widely distributed in animal tissues and has diverse pharmacological effects. However, the role of taurine in modulating smooth muscle contractility is still controversial. We propose that taurine (5-80 mM) can exert bidirectional modulation on the contractility of isolated rat jejunal segments. Different low and high contractile states were induced in isolated jejunal segments of rats to observe the effects of taurine and the associated mechanisms. Taurine induced stimulatory effects on the contractility of isolated rat jejunal segments at 3 different low contractile states, and inhibitory effects at 3 different high contractile states. Bidirectional modulation was not observed in the presence of verapamil or tetrodotoxin, suggesting that taurine-induced bidirectional modulation is Ca2+ dependent and requires the presence of the enteric nervous system. The stimulatory effects of taurine on the contractility of isolated jejunal segments was blocked by atropine but not by diphenhydramine or by cimetidine, suggesting that muscarinic-linked activation was involved in the stimulatory effects when isolated jejunal segments were in a low contractile state. The inhibitory effects of taurine on the contractility of isolated jejunal segments were blocked by propranolol and L-NG-nitroarginine but not by phentolamine, suggesting that adrenergic β receptors and a nitric oxide relaxing mechanism were involved when isolated jejunal segments were in high contractile states. No bidirectional effects of taurine on myosin phosphorylation were observed. The contractile states of jejunal segments determine taurine-induced stimulatory or inhibitory effects, which are associated with muscarinic receptors and adrenergic β receptors, and a nitric oxide associated relaxing mechanism.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2014001201068&lng=en&tlng=enTaurineBidirectional modulationEnteric nervous systemCalcium dependentHomeostasisIntestinal motility
spellingShingle Q.Y. Yao
D.P. Chen
D.M. Ye
Y.P. Diao
Y. Lin
Modulatory effects of taurine on jejunal contractility
Brazilian Journal of Medical and Biological Research
Taurine
Bidirectional modulation
Enteric nervous system
Calcium dependent
Homeostasis
Intestinal motility
title Modulatory effects of taurine on jejunal contractility
title_full Modulatory effects of taurine on jejunal contractility
title_fullStr Modulatory effects of taurine on jejunal contractility
title_full_unstemmed Modulatory effects of taurine on jejunal contractility
title_short Modulatory effects of taurine on jejunal contractility
title_sort modulatory effects of taurine on jejunal contractility
topic Taurine
Bidirectional modulation
Enteric nervous system
Calcium dependent
Homeostasis
Intestinal motility
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2014001201068&lng=en&tlng=en
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