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Effects of hypoxia and glucose-removal condition on muscle contraction of the smooth muscles of porcine urinary bladder
To elucidate the dependence of aerobic energy metabolism and utilization of glucose in contraction of urinary bladder smooth muscle, we investigated the changes in the reduced pyridine nucleotide (PNred) fluorescence, representing glycolysis activity, and determined the phosphocreatine (PCr) and ATP...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751117/ https://www.ncbi.nlm.nih.gov/pubmed/26369431 http://dx.doi.org/10.1292/jvms.15-0269 |
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author | NAGAI, Yuta KANEDA, Takeharu MIYAMOTO, Yasuyuki NURUKI, Takaomi KANDA, Hidenori URAKAWA, Norimoto SHIMIZU, Kazumasa |
author_facet | NAGAI, Yuta KANEDA, Takeharu MIYAMOTO, Yasuyuki NURUKI, Takaomi KANDA, Hidenori URAKAWA, Norimoto SHIMIZU, Kazumasa |
author_sort | NAGAI, Yuta |
collection | PubMed |
description | To elucidate the dependence of aerobic energy metabolism and utilization of glucose in contraction of urinary bladder smooth muscle, we investigated the changes in the reduced pyridine nucleotide (PNred) fluorescence, representing glycolysis activity, and determined the phosphocreatine (PCr) and ATP contents of the porcine urinary bladder during contractions induced by high K(+) or carbachol (CCh) and with and without hypoxia (achieved by bubbling N(2) instead of O(2)) or in a glucose-free condition. Hyperosmotic addition of 65 mM KCl (H-65K(+)) and 1 µM CCh induced a phasic contraction followed by a tonic contraction. A glucose-free physiological salt solution (PSS) did not change the subsequent contractile responses to H-65K(+) and CCh. However, hypoxia significantly attenuated H-65K(+)- and CCh-induced contraction. H-65K(+) and CCh induced a sustained increase in PNred fluorescence, representing glycolysis activity. Hypoxia enhanced H-65K(+)- and CCh-induced increases in PNred fluorescence, whereas glucose-free PSS decreased these increases, significantly. In the presence of H-65K(+), hypoxia decreased the PCr and ATP contents; however, the glucose-free PSS did not change the PCr contents. In conclusion, we demonstrated that high K(+)- and CCh-induced contractions depend on aerobic metabolism and that an endogenous substrate may be utilized to maintain muscle contraction in a glucose-free PSS in the porcine urinary bladder. |
format | Online Article Text |
id | pubmed-4751117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47511172016-02-26 Effects of hypoxia and glucose-removal condition on muscle contraction of the smooth muscles of porcine urinary bladder NAGAI, Yuta KANEDA, Takeharu MIYAMOTO, Yasuyuki NURUKI, Takaomi KANDA, Hidenori URAKAWA, Norimoto SHIMIZU, Kazumasa J Vet Med Sci Pharmacology To elucidate the dependence of aerobic energy metabolism and utilization of glucose in contraction of urinary bladder smooth muscle, we investigated the changes in the reduced pyridine nucleotide (PNred) fluorescence, representing glycolysis activity, and determined the phosphocreatine (PCr) and ATP contents of the porcine urinary bladder during contractions induced by high K(+) or carbachol (CCh) and with and without hypoxia (achieved by bubbling N(2) instead of O(2)) or in a glucose-free condition. Hyperosmotic addition of 65 mM KCl (H-65K(+)) and 1 µM CCh induced a phasic contraction followed by a tonic contraction. A glucose-free physiological salt solution (PSS) did not change the subsequent contractile responses to H-65K(+) and CCh. However, hypoxia significantly attenuated H-65K(+)- and CCh-induced contraction. H-65K(+) and CCh induced a sustained increase in PNred fluorescence, representing glycolysis activity. Hypoxia enhanced H-65K(+)- and CCh-induced increases in PNred fluorescence, whereas glucose-free PSS decreased these increases, significantly. In the presence of H-65K(+), hypoxia decreased the PCr and ATP contents; however, the glucose-free PSS did not change the PCr contents. In conclusion, we demonstrated that high K(+)- and CCh-induced contractions depend on aerobic metabolism and that an endogenous substrate may be utilized to maintain muscle contraction in a glucose-free PSS in the porcine urinary bladder. The Japanese Society of Veterinary Science 2015-09-14 2016-01 /pmc/articles/PMC4751117/ /pubmed/26369431 http://dx.doi.org/10.1292/jvms.15-0269 Text en ©2016 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Pharmacology NAGAI, Yuta KANEDA, Takeharu MIYAMOTO, Yasuyuki NURUKI, Takaomi KANDA, Hidenori URAKAWA, Norimoto SHIMIZU, Kazumasa Effects of hypoxia and glucose-removal condition on muscle contraction of the smooth muscles of porcine urinary bladder |
title | Effects of hypoxia and glucose-removal condition on muscle contraction of the
smooth muscles of porcine urinary bladder |
title_full | Effects of hypoxia and glucose-removal condition on muscle contraction of the
smooth muscles of porcine urinary bladder |
title_fullStr | Effects of hypoxia and glucose-removal condition on muscle contraction of the
smooth muscles of porcine urinary bladder |
title_full_unstemmed | Effects of hypoxia and glucose-removal condition on muscle contraction of the
smooth muscles of porcine urinary bladder |
title_short | Effects of hypoxia and glucose-removal condition on muscle contraction of the
smooth muscles of porcine urinary bladder |
title_sort | effects of hypoxia and glucose-removal condition on muscle contraction of the
smooth muscles of porcine urinary bladder |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751117/ https://www.ncbi.nlm.nih.gov/pubmed/26369431 http://dx.doi.org/10.1292/jvms.15-0269 |
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