Title |
Subtype-selective GABAA receptor mimetics—novel antihyperalgesic agents?
|
---|---|
Published in |
Journal of Molecular Medicine, March 2009
|
DOI | 10.1007/s00109-009-0454-3 |
Pubmed ID | |
Authors |
Hanns Ulrich Zeilhofer, Robert Witschi, Katharina Hösl |
Abstract |
Agonists at the benzodiazepine-binding site of ionotropic gamma-aminobutyric acid (GABA(A)) receptors are in clinical use as hypnotics, anxiolytics, and anticonvulsants since the early 1960. Analgesic effects of classical benzodiazepines have occasionally been reported in certain subgroups of patients suffering from chronic pain or after spinal delivery through intrathecal catheters. However, these drugs are generally not considered as analgesics but should in fact be avoided in patients with chronic pain. Recent evidence from genetically modified mice now indicates that agents targeting only a subset of benzodiazepine (GABA(A)) receptors should provide pronounced antihyperalgesic activity against inflammatory and neuropathic pain. Several such compounds have been developed recently, which exhibit significant antihyperalgesia in mice and rats and appear to be devoid of the typical side-effects of classical benzodiazepines. |
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Geographical breakdown
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Austria | 2 | 6% |
Germany | 1 | 3% |
United States | 1 | 3% |
Unknown | 29 | 88% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 7 | 21% |
Student > Master | 7 | 21% |
Student > Bachelor | 4 | 12% |
Professor > Associate Professor | 4 | 12% |
Researcher | 3 | 9% |
Other | 6 | 18% |
Unknown | 2 | 6% |
Readers by discipline | Count | As % |
---|---|---|
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Neuroscience | 5 | 15% |
Pharmacology, Toxicology and Pharmaceutical Science | 4 | 12% |
Chemistry | 2 | 6% |
Other | 3 | 9% |
Unknown | 3 | 9% |