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Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle
This study was designed to investigate the effects of polyamines on mechanical contraction and voltage-dependent calcium current (VDCC) of guinea-pig gastric smooth muscle. Mechanical contraction and calcium channel current (I(Ba)) were recorded by isometric tension recording and whole-cell patch cl...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693568/ https://www.ncbi.nlm.nih.gov/pubmed/17297251 http://dx.doi.org/10.3346/jkms.2007.22.1.48 |
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author | Kim, Young Chul Sim, Jae Hoon Kim, Young Ho Kwon, Seong-Chun Lee, Sang Jin Kim, Seung Ryul Kim, Dong Woon Park, Seon-Mee Youn, Sei Jin Lee, Sang-Jeon Xing, De-Gang Xu, Wen-Xie Kim, Ki Whan |
author_facet | Kim, Young Chul Sim, Jae Hoon Kim, Young Ho Kwon, Seong-Chun Lee, Sang Jin Kim, Seung Ryul Kim, Dong Woon Park, Seon-Mee Youn, Sei Jin Lee, Sang-Jeon Xing, De-Gang Xu, Wen-Xie Kim, Ki Whan |
author_sort | Kim, Young Chul |
collection | PubMed |
description | This study was designed to investigate the effects of polyamines on mechanical contraction and voltage-dependent calcium current (VDCC) of guinea-pig gastric smooth muscle. Mechanical contraction and calcium channel current (I(Ba)) were recorded by isometric tension recording and whole-cell patch clamp technique. Spermine, spermidine and putrescine inhibited spontaneous contraction of the gastric smooth muscle in a concentration-dependent manner. Spermine (2 mM) reduced high K(+) (50 mM)-induced contraction to 16±6.4% of the control (n=9), and significantly inhibited I(Ba) in a reversible manner (p<0.05; IC(50)=0.8 mM). Pre- and post-treatment of tissue with spermine (2-5 mM, n=10) also inhibited acetylcholine (10 µM)-induced phasic contraction to 5±6.4% of the control. Inhibitory effect of spermine on I(Ba) was observed at a wide range of test potentials of current/voltage (I/V) relationship (p<0.05), and steady-state activation of I(Ba) was shifted to the right by spermine (p<0.05). Spermidine and putrescine (1 mM each) also inhibited I(Ba) to 51±5.7% and 81±5.3% of the control, respectively. And putrescine (1 mM) inhibited I(Ba) at whole tested potentials (p<0.05) without significant change of kinetics (p<0.05). Finally, 5 mM putrescine also inhibited high K(+)-induced contraction to 53±7.1% of the control (n=4). These findings suggest that polyamines inhibit contractions of guinea-pig gastric smooth muscle via inhibition of VDCC. |
format | Text |
id | pubmed-2693568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-26935682009-06-11 Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle Kim, Young Chul Sim, Jae Hoon Kim, Young Ho Kwon, Seong-Chun Lee, Sang Jin Kim, Seung Ryul Kim, Dong Woon Park, Seon-Mee Youn, Sei Jin Lee, Sang-Jeon Xing, De-Gang Xu, Wen-Xie Kim, Ki Whan J Korean Med Sci Original Article This study was designed to investigate the effects of polyamines on mechanical contraction and voltage-dependent calcium current (VDCC) of guinea-pig gastric smooth muscle. Mechanical contraction and calcium channel current (I(Ba)) were recorded by isometric tension recording and whole-cell patch clamp technique. Spermine, spermidine and putrescine inhibited spontaneous contraction of the gastric smooth muscle in a concentration-dependent manner. Spermine (2 mM) reduced high K(+) (50 mM)-induced contraction to 16±6.4% of the control (n=9), and significantly inhibited I(Ba) in a reversible manner (p<0.05; IC(50)=0.8 mM). Pre- and post-treatment of tissue with spermine (2-5 mM, n=10) also inhibited acetylcholine (10 µM)-induced phasic contraction to 5±6.4% of the control. Inhibitory effect of spermine on I(Ba) was observed at a wide range of test potentials of current/voltage (I/V) relationship (p<0.05), and steady-state activation of I(Ba) was shifted to the right by spermine (p<0.05). Spermidine and putrescine (1 mM each) also inhibited I(Ba) to 51±5.7% and 81±5.3% of the control, respectively. And putrescine (1 mM) inhibited I(Ba) at whole tested potentials (p<0.05) without significant change of kinetics (p<0.05). Finally, 5 mM putrescine also inhibited high K(+)-induced contraction to 53±7.1% of the control (n=4). These findings suggest that polyamines inhibit contractions of guinea-pig gastric smooth muscle via inhibition of VDCC. The Korean Academy of Medical Sciences 2007-02 2007-02-28 /pmc/articles/PMC2693568/ /pubmed/17297251 http://dx.doi.org/10.3346/jkms.2007.22.1.48 Text en Copyright © 2007 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Young Chul Sim, Jae Hoon Kim, Young Ho Kwon, Seong-Chun Lee, Sang Jin Kim, Seung Ryul Kim, Dong Woon Park, Seon-Mee Youn, Sei Jin Lee, Sang-Jeon Xing, De-Gang Xu, Wen-Xie Kim, Ki Whan Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle |
title | Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle |
title_full | Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle |
title_fullStr | Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle |
title_full_unstemmed | Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle |
title_short | Effects of Polyamines on Contractility of Guinea-Pig Gastric Smooth Muscle |
title_sort | effects of polyamines on contractility of guinea-pig gastric smooth muscle |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693568/ https://www.ncbi.nlm.nih.gov/pubmed/17297251 http://dx.doi.org/10.3346/jkms.2007.22.1.48 |
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