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Noise and Relaxation Studies of Acetylcholine Induced Currents in the Presence of Procaine

Overview
Journal J Physiol
Specialty Physiology
Date 1978 May 1
PMID 671293
Citations 21
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Abstract

1. The effects of procaine on the excitatory effects of acetylcholine (ACh) on Aplysia neurones were studied by analysing the current relaxations induced by voltage steps. Procaine was applied by perfusion and ACh was applied iontophoretically under two sets of experimental conditions designed to produce very different ACh concentrations at the membrane. 2. When ACh was applied at high concentration, the current relaxation following a hyperpolarizing step showed two components at procaine concentrations of about 2 X 10(-5) M; a fast increase was followed by a slow decrease. At high procaine concentrations (greater than 10(-4) M), the relaxation has only one component, corresponding to an exponential current decrease. 3. When ACh was applied at low concentrations, the current relaxation usually showed two components. At low procaine concentrations a fast increase was followed by a slower one; at higher procaine concentrations, a fast decrease preceded the slow increase. 4. All the results can be accounted for by assuming that procaine binds preferentially to the activated receptor-channel complex and converts it into a non-conducting complex. The association and dissociation constants were calculated to be (at 12 degrees C, -80 mV) 1.3 X 10(6) M-1 sec-1 and 10 sec-1.

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References
1.
Furukawa T . Properties of the procaine end-plate potential. Jpn J Physiol. 1957; 7(3):199-212. DOI: 10.2170/jjphysiol.7.199. View

2.
Ascher P, Marty A, Neild T . The mode of action of antagonists of the excitatory response to acetylcholine in Aplysia neurones. J Physiol. 1978; 278:207-35. PMC: 1282345. DOI: 10.1113/jphysiol.1978.sp012300. View

3.
Ascher P, Marty A, Neild T . Life time and elementary conductance of the channels mediating the excitatory effects of acetylcholine in Aplysia neurones. J Physiol. 1978; 278:177-206. PMC: 1282344. DOI: 10.1113/jphysiol.1978.sp012299. View

4.
Neher E, Steinbach J . Local anaesthetics transiently block currents through single acetylcholine-receptor channels. J Physiol. 1978; 277:153-76. PMC: 1282384. DOI: 10.1113/jphysiol.1978.sp012267. View

5.
Adams P . Voltage jump analysis of procaine action at frog end-plate. J Physiol. 1977; 268(2):291-318. PMC: 1283665. DOI: 10.1113/jphysiol.1977.sp011858. View