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PMID: 2204430 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Mechanism of penetration and of action of local anesthetics in Escherichia coli cells.

Biochimica et biophysica acta ·Vol. 1027 ·No. 3 ·1990-09-07 ·Pages 238-44

Collura V, Letellier L

Abstract

Escherichia coli cells were used to study the mechanism of penetration of local anesthetics and the relationship between permeation and functional properties. We show that both the neutral and the protonated form of dibucaine can be accumulated in the cells. Accumulation of the protonated form occurs in response to a transmembrane electrical potential (negative inside) and results in high trapped concentrations (70 mM). Accumulation can lead to an alkalinization of the internal pH. Low concentrations of dibucaine stimulate the respiration, increase the transmembrane electrical potential and raise the accumulation of solutes. Inhibition of these functions occurs at higher concentrations of the drug. Furthermore, the drug concentration required to inhibit these functions is smaller at alkaline external pH than at acidic external pH, suggesting that the inhibition is mainly due to the neutral form of the anesthetics. Other hydrophobic amines also stimulate and inhibit different membrane functions, their efficiency being correlated to their lipophilicity.

MeSH Terms
Adenosine Triphosphate/metabolism Anesthetics, Local/pharmacokinetics Cell Membrane Permeability/drug effects Dibucaine/pharmacokinetics Escherichia coli/metabolism Hydrogen-Ion Concentration Membrane Potentials/drug effects Oxygen Consumption
Chemicals
Anesthetics, Local Adenosine Triphosphate Dibucaine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Collura V
Laboratoire des Biomembranes, U.A. 1116 CNRS, Université Paris Sud, Orsay, France.
Letellier L
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1990-09-07
Pages
238-44
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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