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THE EFFECT IN VITRO OF VOLATILE ANESTHETICS ON THE ACTIVITY OF CHOLINESTERASES 1
Author(s) -
BRASWELL L. M.,
KITZ R. J.
Publication year - 1977
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1977.tb07784.x
Subject(s) - anesthetic , enflurane , isoflurane , acetylcholinesterase , chemistry , methoxyflurane , aché , in vivo , halothane , potency , in vitro , cholinesterase , enzyme , pharmacology , biochemistry , stereochemistry , anesthesia , organic chemistry , biology , medicine , microbiology and biotechnology
— Because the mechanism of anesthesia is unknown, the relationship between anesthetics and enzymes essential to brain function may be an important one. Therefore, the effect of 8 volatile anesthetics on the enzymatic activity of solubilized, purified dog brain and human erythrocyte acetylcholinesterase (AChE) and human serum cholinesterase (ChE) was studied in vitro. Serum ChE was found to be insensitive to saturated solutions of all the anesthetics studied. However, brain and erythrocyte AChE were reversibly inhibited in a dose‐dependent manner by all 8 anesthetics in concentrations exceeding those used in clinical practice. Kinetic analysis revealed a mixed (competitive, non‐competitive) type of inhibition with the exception of the ether‐crythrocyte AChE interaction which was characterized by competitive inhibition. Ether and methoxyflurane were found to depress the AChE activity the most and isoflurane and enflurane the least. The concentrations of anesthetic in the gas phase necessary for 50% inhibition of erythrocyte AChE activity (I 50 ) were calculated for 5 anesthetics and found to correlate with their water‐gas partition coefficients. These data suggest that the effect in vitro of volatile anesthetics on the catalytic activity of cholinesterases is a variable one and may be unrelated to anesthetic potency in vivo. The implications of these data concerning anesthetic‐active site interactions are discussed.