Kolaeva S H, Lee T F, Wang L C, Paproski S M
Institute of Biological Physics, U.S.S.R. Academic of Sciences, Pushchino, Moscow Region.
Brain Res Bull. 1990 Sep;25(3):407-10. doi: 10.1016/0361-9230(90)90228-r.
Intracerebroventricular injection of neokyotorphin (NKT) (0.5-2.0 micrograms) caused a dose-related increase in body temperature (Tb) of rats maintained at 28 degrees C. The change in Tb of the rat induced by the optimal dose of NKT (1 microgram) was attenuated when the rat was exposed to 18 degrees C. At both ambient temperatures, heat production was not affected but heat loss was significantly reduced at 28 degrees C in rats receiving 1 microgram NKT. Pretreatment with naloxone (5 mg/kg, IP) significantly reduced the hyperthermic effect induced by NKT (1 microgram). These results suggest that NKT can affect the prevailing thermoregulatory heat loss activities and this effect may be mediated through stimulated release of endogenous opioids.
向脑室内注射新强啡肽(NKT)(0.5 - 2.0微克)会使处于28摄氏度环境下的大鼠体温(Tb)呈剂量依赖性升高。当大鼠处于18摄氏度环境时,由最佳剂量NKT(1微克)诱导的大鼠Tb变化减弱。在两种环境温度下,接受1微克NKT的大鼠产热未受影响,但在28摄氏度时散热显著减少。用纳洛酮(5毫克/千克,腹腔注射)预处理可显著降低NKT(1微克)诱导的体温过高效应。这些结果表明,NKT可影响主要的体温调节散热活动,且这种效应可能通过刺激内源性阿片类物质释放来介导。