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Evaluation of autoreceptor-mediated control of [3H]acetylcholine release in rat and human neocortex
Authors:C. Albrecht  H. G. Bloss  R. Jackisch  T. J. Feuerstein
Affiliation:Sektion Klinische Neuropharmakologie der Neurologischen Universit?tsklinik, Neurozentrum, Breisacher Strasse 64, D-79106 Freiburg, Germany, e-mail: feuer@ukl.uni-freiburg.de, Tel.: +49-761-270-5280, Fax: +49-761-270-5281, DE
Neurochirurgische Universit?tsklinik, Neurozentrum, Breisacher Strasse 64, D-79106 Freiburg, Germany, DE
Pharmakologisches Institut der Universit?t Freiburg, Hansastrasse 9a, D-79104 Freiburg, Germany, DE
Abstract:In order to assess the autoinhibitory control of endogenous acetylcholine (ACh) in rat and human neocortex, slices of these tissues were prelabelled with [(3)H]choline, superfused continuously and stimulated electrically using various frequencies in the presence or absence of drugs. The autoinhibitory feedback control of [(3)H]ACh release was operative - despite the absence of blockers of ACh esterase - at stimulation frequencies >/= 3 Hz in rat and >/= 6 Hz in human neocortex tissue. At these frequencies the muscarinic antagonist atropine (0.1 microM) disinhibited the release of [(3)H]ACh in both species. Estimation of the biophase concentration of ACh near the autoreceptor in the rat neocortex from concentration-response curves of the muscarinic agonist oxotremorine revealed that at 3 Hz about 25% of the autoreceptors were activated by endogenously released ACh. This estimation is consistent with an increase in [(3)H]ACh release to about 120% of control values by complete blockade of autoreceptors with atropine. The observation that in human neocortical tissue presynaptic autoinhibition of [(3)H]ACh release is operative at stimulation frequencies >/= 6 Hz suggests that selective blockade of autoinhibition may also increase ACh release in the cortex of Alzheimer's disease patients, without additional blockade of the enzyme acetylcholinesterase.
Keywords:  Human neocortex  Rat neocortex  Acetylcholine release  Autoinhibition  Alzheimer’  s disease
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