Journal
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 393, Issue 1-3, Pages 179-195Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/S0014-2999(00)00009-1
Keywords
GTS-21; 40H-GTS-21; alpha 7 receptor-selective agonist
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Funding
- NINDS NIH HHS [NS32888-02] Funding Source: Medline
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The alpha 7-selective agonists 3-(2,4-dimethoxybenzylidene)-anabaseine (GTS-21), also known as DMXB, and 3-(4-hydroxy,2-methoxybenzylidene)anabaseine (4OH-GTS-21) produce a variety of behavioral and cytoprotective effects that may be related to the activation of either large transient currents at high concentrations or small sustained currents at lower agonist concentrations. We are using acutely dissociated hypothalamic neurons, which express a central nervous system (CNS) alpha 7-type receptor, to test a model for the concentration-dependent desensitization of alpha 7-mediated responses. Our results confirm that 40H-GTS-21 is a potent activator of neuronal alpha 7 nicotinic-acetylcholine receptor. The rapid application of agonist leads to a brief period of maximal receptor-activation followed by desensitization. Rise rates, decay rates, and the degree to which current was desensitized were all concentration-dependent. Following the initial peak response to a 300-mu M 4OH-GTS-21 application, current is reduced to baseline values within about 100 ms. Application of 30 mu M 40H-GTS-21 produced both a transient peak current and a sustained current that decayed only slowly after the removal of agonist. In the case of a 300-mu M 40H-GTS-21 application, after agonist was removed, we saw a rebound response up to the level of the 30-mu M sustained current. The data, therefore, suggest that a sufficient level of agonist occupation can be retained on the receptor to promote activation for up to several hundred milliseconds. (C) 2000 Elsevier Science B.V. All rights reserved.
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