Ulugol, ADost, TDokmeci, DAkpolat, MKaradag, CHDokmeci, I2024-06-122024-06-1220000300-9564https://doi.org/10.1007/s007020070074https://hdl.handle.net/20.500.14551/22735Morphine has long been known to have potent effects on body temperature. It has been suggested that both N-methl-D-aspartate (NMDA) receptors and nitric oxide (NO) pathway are involved in thermoregulation and also known to play important roles in some of morphine effects. The aim of this study was therefore to investigate the contribution of NMDA receptors and NO to the thermoregulatory effect of morphine. Morphine produced a hypothermic effect, especially at the dose of 10 mg/kg. Ketamine (5-40 mg/kg, i.p.) and N-G-nitro-L-arginine-methyl ester (L-Name, 1-100 mg/kg i.p.) also produced hypothermic effects with their higher doses. At doses which themselves produced no effect on colonic temperature in mice, both ketamine (10 mg/kg, i.p.) and L-NAME (10 mg/kg, i.p.) enhanced the hypothermic effect of morphine (10 mg/kg i.p.). These results further support the relationship between NO and NMDA receptors and suggest a possible role of NMDA-NO pathway in the thermoregulatory effect of morphine.en10.1007/s007020070074info:eu-repo/semantics/closedAccessNMDANitric OxideMorphineHypothermiaCompetitive AntagonistPlace PreferenceNervous-SystemSpinal-CordRatInhibitionToleranceSynthaseInterleukin-1-BetaAcetylcholineArticle1075515521Q2WOS:0000869879000012-s2.0-003405972011072747Q2