| Literature DB >> 16246435 |
Linda R Watkins1, Mark R Hutchinson, Ian N Johnston, Steven F Maier.
Abstract
Development of analgesic tolerance and withdrawal-induced pain enhancement present serious difficulties for the use of opioids for pain control. Although neuronal mechanisms to account for these phenomena have been sought for many decades, their bases remain unresolved. Within the past four years, a novel non-neuronal candidate has been uncovered that opposes acute opioid analgesia and contributes to development of opioid tolerance and tolerance-associated pain enhancement. This novel candidate is spinal cord glia. Glia are important contributors to the creation of enhanced pain states via the release of neuroexcitatory substances. New data suggest that glia also release neuroexcitatory substances in response to morphine, thereby opposing its effects. Controlling glial activation could therefore increase the clinical utility of analgesic drugs.Entities:
Mesh:
Substances:
Year: 2005 PMID: 16246435 DOI: 10.1016/j.tins.2005.10.001
Source DB: PubMed Journal: Trends Neurosci ISSN: 0166-2236 Impact factor: 13.837