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Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel
We have studied the effect of local anesthetics QX 572, which is permanently charged, and benzocaine, which is neutral, on batrachotoxin- activated sodium channels in mouse neuroblastoma N18 cells. The dose- response curves for each drug suggest that QX 752 and benzocaine each act on a single class...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1981
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2215428/ https://www.ncbi.nlm.nih.gov/pubmed/6267160 |
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collection | PubMed |
description | We have studied the effect of local anesthetics QX 572, which is permanently charged, and benzocaine, which is neutral, on batrachotoxin- activated sodium channels in mouse neuroblastoma N18 cells. The dose- response curves for each drug suggest that QX 752 and benzocaine each act on a single class of binding sites. The dissociation constants are 3.15 X 10(-5) M for QX 572 and 2.65 X 10(-4) M for benzocaine. Equilibrium and kinetic experiments indicate that both drugs are competitive inhibitors of batrachotoxin. When benzocaine and QX 572 are present with batrachotoxin, they are much more effective at inhibiting Na+ flux than would be predicted by a one-site model. Our results indicate that QX 572 and benzocaine bind to separate sites, each of which interacts competitively with batrachotoxin. |
format | Text |
id | pubmed-2215428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1981 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22154282008-04-23 Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel J Gen Physiol Articles We have studied the effect of local anesthetics QX 572, which is permanently charged, and benzocaine, which is neutral, on batrachotoxin- activated sodium channels in mouse neuroblastoma N18 cells. The dose- response curves for each drug suggest that QX 752 and benzocaine each act on a single class of binding sites. The dissociation constants are 3.15 X 10(-5) M for QX 572 and 2.65 X 10(-4) M for benzocaine. Equilibrium and kinetic experiments indicate that both drugs are competitive inhibitors of batrachotoxin. When benzocaine and QX 572 are present with batrachotoxin, they are much more effective at inhibiting Na+ flux than would be predicted by a one-site model. Our results indicate that QX 572 and benzocaine bind to separate sites, each of which interacts competitively with batrachotoxin. The Rockefeller University Press 1981-02-01 /pmc/articles/PMC2215428/ /pubmed/6267160 Text en 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 Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel |
title | Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel |
title_full | Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel |
title_fullStr | Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel |
title_full_unstemmed | Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel |
title_short | Local anesthetics QX 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel |
title_sort | local anesthetics qx 572 and benzocaine act at separate sites on the batrachotoxin-activated sodium channel |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2215428/ https://www.ncbi.nlm.nih.gov/pubmed/6267160 |