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Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification

Conductance of gap junctions in many preparations has been shown to be sensitive to cytoplasmic pH, decreasing as pH decreases below 7.5 in fish and amphibian embryos and below 7.1 in crayfish septate axon. We have found a new class of compounds, benzyl acetate derivatives, that reversibly decrease...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275633/
https://www.ncbi.nlm.nih.gov/pubmed/6736125
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description Conductance of gap junctions in many preparations has been shown to be sensitive to cytoplasmic pH, decreasing as pH decreases below 7.5 in fish and amphibian embryos and below 7.1 in crayfish septate axon. We have found a new class of compounds, benzyl acetate derivatives, that reversibly decrease junctional conductance, gj, when applied in low concentration (approximately 1 mM). Simultaneous intracellular pH (pHi) measurements show that the ester effects are attributable to reduction in pHi. The sensitivity of gj to these compounds and the relative lack of side effects make these agents attractive for studies of the role played by gap junctions in normal tissue function. In addition, the finding of cytoplasmic acidification in response to cell exposure to esters suggests caution in interpretation of results obtained using esterified compounds for intracellular loading.
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spelling pubmed-22756332008-05-01 Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification J Cell Biol Articles Conductance of gap junctions in many preparations has been shown to be sensitive to cytoplasmic pH, decreasing as pH decreases below 7.5 in fish and amphibian embryos and below 7.1 in crayfish septate axon. We have found a new class of compounds, benzyl acetate derivatives, that reversibly decrease junctional conductance, gj, when applied in low concentration (approximately 1 mM). Simultaneous intracellular pH (pHi) measurements show that the ester effects are attributable to reduction in pHi. The sensitivity of gj to these compounds and the relative lack of side effects make these agents attractive for studies of the role played by gap junctions in normal tissue function. In addition, the finding of cytoplasmic acidification in response to cell exposure to esters suggests caution in interpretation of results obtained using esterified compounds for intracellular loading. The Rockefeller University Press 1984-07-01 /pmc/articles/PMC2275633/ /pubmed/6736125 Text en Copyright © 1984, This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification
title Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification
title_full Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification
title_fullStr Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification
title_full_unstemmed Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification
title_short Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification
title_sort substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275633/
https://www.ncbi.nlm.nih.gov/pubmed/6736125