Harvey J A, Welsh S E, Hood H, Romano A G
Department of Pharmacology, Allegheny University of the Health Sciences, Philadelphia, PA 19129, USA.
Psychopharmacology (Berl). 1999 Jan;141(2):162-8. doi: 10.1007/s002130050820.
This study examined the role of the serotonin 5-HT2 receptor in motor function by examining the effect of antagonists on the motor performance of a cranial nerve reflex, the nictitating membrane (NM) reflex of the rabbit. The NM reflex was elicited by varying intensities of a tactile stimulus and the magnitudes of the elicited responses were measured at each intensity. Dose-response curves were obtained for the effects of several 5-HT2 receptor antagonists on response magnitude. d-Bro-molysergic acid diethylamide (BOL), LY-53,857 and ketanserin had no significant effect on the magnitude of the NM reflex, indicating that they are neutral antagonists. However, the 5-HT2 receptor antagonists ritanserin, MDL-11,939 and mianserin produced a significant reduction in response magnitude with no significant effects on response frequency, suggesting that they were acting as inverse agonists at the 5-HT2 receptor. The reduction in reflex magnitude produced by mianserin (10 micromol/kg) was fully blocked by BOL (5.8 micromol/kg), supporting the conclusion that mianserin was producing a reduction in reflex magnitude through an effect at the 5-HT2 receptor. The occurrence of inverse agonism suggests the possible existence of constitutive activity in vivo. We conclude that the 5-HT2 receptor (either 2A or 2C) plays an important role in motor function, perhaps by providing a tonic influence on motor systems.
本研究通过检测拮抗剂对家兔脑神经反射——瞬膜(NM)反射运动表现的影响,来探讨5-羟色胺5-HT2受体在运动功能中的作用。通过改变触觉刺激的强度来引发NM反射,并在每种强度下测量引发反应的幅度。获得了几种5-HT2受体拮抗剂对反应幅度影响的剂量反应曲线。d-溴麦角酸二乙酰胺(BOL)、LY-53,857和酮色林对NM反射的幅度没有显著影响,表明它们是中性拮抗剂。然而,5-HT2受体拮抗剂利坦色林、MDL-11,939和米安色林使反应幅度显著降低,而对反应频率没有显著影响,这表明它们在5-HT2受体上作为反向激动剂起作用。米安色林(10微摩尔/千克)引起的反射幅度降低被BOL(5.8微摩尔/千克)完全阻断,这支持了米安色林通过对5-HT2受体的作用导致反射幅度降低的结论。反向激动作用的出现表明体内可能存在组成性活性。我们得出结论,5-HT2受体(2A或2C)在运动功能中起重要作用,可能是通过对运动系统提供一种紧张性影响。