Hasegawa Y, Ono H
Department of Pharmacy, University of Tokyo, Japan.
Eur J Pharmacol. 1996 Jan 11;295(2-3):211-4. doi: 10.1016/0014-2999(95)00759-8.
In the present study, we examined the effect of the 5-HT1A receptor agonist (+/-)-8-hydroxy-2-(di-n-propylamino)tetralin hydrobromide (8-OH-DPAT), on the mono- and polysynaptic reflexes in intact and spinalized rats. 8-OH-DPAT (10 micrograms/kg i.v.) significantly potentiated the amplitude of the monosynaptic reflex in intact rats. In contrast, 8-OH-DPAT (30 and 100 micrograms/kg i.v.) produced a significant dose-related inhibition of the amplitude of the monosynaptic reflex in spinalized rats. These results suggest that 8-OH-DPAT predominantly excites spinal motor systems at the supraspinal site, and inhibits such systems at a spinal cord site.
在本研究中,我们检测了5-羟色胺1A受体激动剂(±)-8-羟基-2-(二正丙基氨基)四氢萘氢溴酸盐(8-OH-DPAT)对完整大鼠和脊髓横断大鼠单突触和多突触反射的影响。8-OH-DPAT(静脉注射10微克/千克)显著增强了完整大鼠单突触反射的幅度。相反,8-OH-DPAT(静脉注射30和100微克/千克)对脊髓横断大鼠的单突触反射幅度产生了显著的剂量依赖性抑制。这些结果表明,8-OH-DPAT主要在脊髓以上部位兴奋脊髓运动系统,而在脊髓部位抑制该系统。