Effects of calcium channel antagonists and Bay K 8644 on the analgesic response to pentazocine and U 50488H
Author
dc.contributor.author
Quijada, L.
Author
dc.contributor.author
Germany, A.
Author
dc.contributor.author
Hernández, A.
Author
dc.contributor.author
Contreras, E.
Admission date
dc.date.accessioned
2018-12-20T14:34:19Z
Available date
dc.date.available
2018-12-20T14:34:19Z
Publication date
dc.date.issued
1992
Cita de ítem
dc.identifier.citation
General Pharmacology, Volumen 23, Issue 5, 2018, Pages 837-842
Identifier
dc.identifier.issn
03063623
Identifier
dc.identifier.other
10.1016/0306-3623(92)90234-B
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/156497
Abstract
dc.description.abstract
1. 1. The effects of diltiazem, nifedipine and verapamil and the calcium channel agonist Bay K 8644 on the analgesic responses to the subcutaneous (s.c.) or intracerebroventricular (i.c.v.) administration of pentazocine and U 50488H were investigated in mice. 2. 2. The three calcium channel antagonists and Bay K 8644 reduced the number of writhes induced by the intraperitoneal administration of acetic acid. 3. 3. The analgesic responses to the low doses of pentazocine (s.c.) were additive with the effects of diltiazem, nifedipine or Bay K 8644; while, in contrast, the higher doses produced underadditive responses. Only verapamil increased the effects of the i.c.v. administration of the opioid. 4. 4. The effects of U 50488H (s.c.) were additive with those of diltiazem and Bay K 8644; verapamil only increased the response to the lower dose of the opioid. Nifedipine plus pentazocine always induced underadditive responses. The i.c.v. effects of U 50488H were only increased by verapamil. 5.