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Relaxation measurements on the acetylcholine receptor.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 1975 Sep; Vol. 72 (9), pp. 3496-500. - Publication Year :
- 1975
-
Abstract
- In Electrophorus electroplaques, the agonist-induced postsynaptic conductance depends on membrane potential. During steady exposure to agonists, after a voltage step the conductance relaxes on a millisecond time scale, exponentially approaching a new equilibrium value. The relaxation rate constant k is an instantaneous function of voltage, insensitive to the past or present conductance. Two components sum to form k. A concentration-sensitive component increases linearly with agonist concentration and decreases during desensitization or exposure to curare. Thus this component reflects the average frequency at which acetylcholine receptors are opening. The voltage-sensitive component, obtained by extrapolating k to zero agonist concentration, increases at more positive potentials. For acetylcholine, the voltage-sensitive component equals the rate constant for the exponential decay of postsynaptic currents; it thus seems to be the closing rate for active receptors. The voltage-sensitive component has the relative amplitudes acetylcholine less than carbamoylcholine less than decamethonium, and for each agonist equals the closing rate determined from "noise" measurements at neuromuscular junctions. The kinetic data explain several aspects of the steady-state conductance induced by agonists, but shed no light on apparent cooperative effects.
- Subjects :
- Acetylcholine pharmacology
Action Potentials
Animals
Carbachol pharmacology
Decamethonium Compounds pharmacology
Dose-Response Relationship, Drug
Electric Organ metabolism
Electrophorus
Kinetics
Membrane Potentials
Models, Neurological
Structure-Activity Relationship
Acetylcholine metabolism
Receptors, Cholinergic drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 0027-8424
- Volume :
- 72
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 1059136
- Full Text :
- https://doi.org/10.1073/pnas.72.9.3496