Abstract: | Present study revealed the stimulatory effects of δ opioid receptor on intracellular Ca2+ concentration (Ca2+]i) in SH-SY5Y cells. Fura-2 based single cell fluorescence ratio (F345/F380) was used to monitor the fluctuation of Ca2+]i. Application of the selective delta-opioid receptor agonist alone, D-Pen2,5]-enkephalin (DPDPE), hardly had any effects on cells cultivated for 3–10 days. However, after the cells had been pre-stimulated with cholinoceptor agonist, carbachol, variable calcium elevation was found in 59% of the cultures. The response was naltridole-reversible and dose-dependent, and was abolished completely by thapsigargin (TG) treatment but not by administration of CdCl2 or 0-Ca2+ bath solutions. DPDPE-mediated Ca2+]i elevation was abolished by pertussis toxin (PTX) pretreatment but not cholera toxin (CTX), indicating coupling via G proteins of Gi/Go subfamily. In 17.5% of the responding cells, biphase response was found which may be due to both the stimulatory and the inhibitory effects of opioid. On the other hand, in acutely dissociated cells, DPPDE alone induced Ca2+]i increase in 50% of the cultures. The probability and the amplitude of the elevation were decreased considerably by application of nifedipine or 0-Ca2+ bath solution and was little affected by application of TG. DPDPE activated Ca2+]i increase via a PTX-insensitive and CTX-sensitive pathway suggesting coupling through Gs subunit. All these indicated the opioid modulated the intracellular Ca2+ regulation system through different pathways. SH-SY5Y cell line might be a suitable model for the investigation of the complex mechanism which underlies opioid function. |