European Journal of Pharmacology, Volumen 217, Issue 2-3, 2018, Pages 137-141
Identifier
dc.identifier.issn
00142999
Identifier
dc.identifier.other
10.1016/0014-2999(92)90833-P
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/161051
Abstract
dc.description.abstract
The antinociceptive action of four Ca2+ channel blockers, nifedipine, nimodipine, verapamil and diltiazem, was evaluated and compared to that of morphine using three algesiometric tests in mice and rats, namely, formalin, writhing and modified hot-plate test. Dose-response curves for all the drugs tested were similar and a significant dose-dependent antinociceptive action was evident in the formalin and writhing tests. However, in the hot-plate test, only nimodipine exhibited a significant analgesic effect, confirming the misleading results previously reported for this test. The findings suggest a pharmacological role of Ca2+ channel blockers in the modulation of antinociception under acute conditions. The analgesic action of Ca2+ channel blockers could be mediated by an increase in the nociceptive threshold resulting from interference with Ca2+ influx at opioid receptors, because Ca2+ influx is critical for the release of neurotransmitters and other substances implicated in nociceptio