Potentiation of Opiate Analgesia and Apparent Reversal of Morphine Tolerance by Proglumide
- 27 April 1984
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 224 (4647), 395-396
- https://doi.org/10.1126/science.6546809
Abstract
Exogenous cholecystokinin selectively antagonizes opiate analgesia, which suggests that endogenous cholecystokinin may act physiologically as an opiate antagonist and may play a role in opiate tolerance. The use of the selective cholecystokinin antagonist proglumide provided a test of these hypotheses in rats that were either inexperienced with or tolerant to opiates. Proglumide potentiated analgesia produced by morphine and endogenous opiates and seemed to reverse tolerance. These results suggest that endogenous cholecystokinin systems oppose the action of opiates.This publication has 10 references indexed in Scilit:
- The formalin test in the mouse: a parametric analysis of scoring propertiesPain, 2000
- Nonspecific convulsions are induced by morphine but notd-Ala2-methionine-enkephalinamide at cortical sitesBrain Research, 1984
- Proglumide: Selective Antagonism of Excitatory Effects of Cholecystokinin in Central Nervous SystemScience, 1983
- Evidence for the Neuropeptide Cholecystokinin as an Antagonist of Opiate AnalgesiaScience, 1983
- Organization of Endogenous Opiate and Nonopiate Pain Control SystemsScience, 1982
- Failure of spinal cord serotonin depletion to alter analgesia elicited from the periaqueductal grayBrain Research, 1982
- Proglumide and benzotript: members of a different class of cholecystokinin receptor antagonists.Proceedings of the National Academy of Sciences, 1981
- Analgesia and ptosis caused by caerulein and cholecystokinin octapeptide (CCK-8)Neuropharmacology, 1980
- Antagonism of acupuncture analgesia in man by the narcotic antagonist naloxoneBrain Research, 1977
- Antagonism of stimulation-produced analgesia by p-CPA, a serotonin synthesis inhibitorBrain Research, 1972