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The channel opening rate of adult‐ and fetal‐type mouse muscle nicotinic receptors activated by acetylcholine
Author(s) -
Maconochie David J.,
Steinbach Joe Henry
Publication year - 1998
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.1998.053bx.x
Subject(s) - nicotinic agonist , acetylcholine receptor , acetylcholine , receptor , chemistry , ion channel , endocrinology , medicine , microbiology and biotechnology , biology , biochemistry
1 expressing either the fetal (Q‐F18) or the adult (Q‐A33) complement of nicotinic acetylcholine receptor subunits derived from mouse skeletal muscle. Pulses of ACh were applied to outside‐out patches of cell membrane by means of a fast perfusion system, at concentrations from 100 nM to 10 mM. We obtained current records with intracellular potentials of ‐60 and +40 mV. The goal of this study was to estimate the channel opening rate. 2 By fitting sums of exponentials to averaged responses, we estimated the rate of development of the current on the application of acetylcholine. The rate constant of the predominant exponential component (the on‐rate) ranges over 3 orders of magnitude, from around 100 s −1 (fetal) at low concentrations of ACh to over 100 000 s −1 (fetal and adult) at the highest concentrations. 3 We establish that our measurement of the on‐rate is not limited by technical constraints, and can therefore be related to the rate constants of a kinetic scheme. Our observations are consistent with a model having a rate‐limiting channel opening step with a forwards rate constant (β) of 80 000 s −1 on average for adult receptors and 60 000 s −1 for fetal receptors, and a minimum opening to closing ratio (β/α) of around 33 (adult) or 50 (fetal). The channel opening rate, β, varies from around 30 000 s −1 to well over 100 000 s −1 for different patches. The large variation cannot all be ascribed to errors of measurement, but indicates patch to patch variation.