{"title":"Cannabinoids Regulate δ-Opioid Receptors in NG108-15 Hybrid Cells","authors":"R. Toro, S. Spampinato","doi":"10.1211/146080800128735962","DOIUrl":null,"url":null,"abstract":"We have studied the effects of long-term activation of cannabinoid receptors on opioid receptor desensitization and down-regulation. The mouse neuroblastomaxrat glioma hybridoma NG 108-15 cell line was used as it represents a suitable model expressing both cannabinoid CB1 and δ-opioid receptors linked to Gi proteins. \n \n \n \nTwenty-four-hour exposure of NG 108-15 cells to the cannabinoid agonist WIN 55, 212-2 mesylate (200 nM) reduced opioid receptor binding, evaluated in intact cells, by approximately 50%. Down-regulation of δ-opioid receptors was not observed in cells exposed to pertussis toxin for 24 h. In cells that were exposed to the cannabinoid for 24 h, the ability of the δ-opioid receptor agonist [D-Ser2, Leu5, Thr6]enkephalin to inhibit forskolin-stimulated cAMP accumulation was significantly attenuated. The selective cannabinoid receptor antagonist SR 141716A blocked the effects elicited by WIN 55,212-2 on δ-opioid receptor desensitization and down-regulation. \n \n \n \nThese data demonstrate the existence, in NG 108-15 cells, of a complex cross-talk between the cannabinoid and opioid receptors.","PeriodicalId":19946,"journal":{"name":"Pharmacy and Pharmacology Communications","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2000-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacy and Pharmacology Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1211/146080800128735962","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We have studied the effects of long-term activation of cannabinoid receptors on opioid receptor desensitization and down-regulation. The mouse neuroblastomaxrat glioma hybridoma NG 108-15 cell line was used as it represents a suitable model expressing both cannabinoid CB1 and δ-opioid receptors linked to Gi proteins.
Twenty-four-hour exposure of NG 108-15 cells to the cannabinoid agonist WIN 55, 212-2 mesylate (200 nM) reduced opioid receptor binding, evaluated in intact cells, by approximately 50%. Down-regulation of δ-opioid receptors was not observed in cells exposed to pertussis toxin for 24 h. In cells that were exposed to the cannabinoid for 24 h, the ability of the δ-opioid receptor agonist [D-Ser2, Leu5, Thr6]enkephalin to inhibit forskolin-stimulated cAMP accumulation was significantly attenuated. The selective cannabinoid receptor antagonist SR 141716A blocked the effects elicited by WIN 55,212-2 on δ-opioid receptor desensitization and down-regulation.
These data demonstrate the existence, in NG 108-15 cells, of a complex cross-talk between the cannabinoid and opioid receptors.