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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-19860

Zeilhofer, H U; Möhler, H; Di Lio, A (2009). GABAergic analgesia: new insights from mutant mice and subtype-selective agonists. Trends in Pharmacological Sciences, 30(8):397-402.

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Abstract

gamma-Aminobutyric acid (GABA) is the most abundant inhibitory neurotransmitter in the brain where it regulates many physiological functions including sleep, anxiety, reward and memory formation. GABAergic neurons and ionotropic GABA(A) receptors are also found in the spinal cord dorsal horn where they control the propagation of pain signals from the periphery to higher central nervous system areas. Recent evidence indicates that diminished inhibitory control at this site is a major factor in chronic pain syndromes. So far, this knowledge could not be translated into clinical pain therapy, probably because of the widespread actions of GABA in the central nervous system. The identification of GABA(A) receptor subtypes responsible for spinal antihyperalgesic effects has recently opened new avenues for the development of subtype-selective modulators of GABA(A) receptors. First results raise hopes that such compounds will be active against inflammatory and neuropathic pain but devoid of many of the side-effects of the established benzodiazepine-like drugs.

Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > Institute of Pharmacology and Toxicology
DDC:570 Life sciences; biology
610 Medicine & health
Language:English
Date:July 2009
Deposited On:22 Jul 2009 12:21
Last Modified:27 Nov 2013 20:46
Publisher:Elsevier
ISSN:0165-6147
Publisher DOI:10.1016/j.tips.2009.05.007
PubMed ID:19616317
Citations:Web of Science®. Times Cited: 40
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