Hasegawa Y, Ono H
Department of Pharmacy, Branch Hospital, Faculty of Medicine, University of Tokyo, Japan.
Brain Res. 1996 Oct 28;738(1):158-61. doi: 10.1016/0006-8993(96)00991-2.
We investigated the effect of 5-HT1A receptor agonist (-/+)-8-hydroxy-2-(di-N-propylamino)tetraline (8-OH-DPAT) and the 5-HT2A/2C receptor agonist (-/+)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI) on monosynaptic transmission in spinalized rats. 8-OH-DPAT significantly inhibited the excitation of alpha-motoneurons evoked by monosynaptic transmission without a direct effect on alpha-motoneuron excitation. DOI potentiated the excitation of alpha-motoneurons by both direct stimulation and monosynaptic transmission. These results indicate that activation of 5-HT1A receptors inhibits monosynaptic transmission, whereas activation of 5-HT2A/2C receptors enhances it.
我们研究了5-羟色胺1A受体激动剂(±)-8-羟基-2-(二-N-丙基氨基)四氢萘(8-OH-DPAT)和5-羟色胺2A/2C受体激动剂(±)-1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(DOI)对脊髓损伤大鼠单突触传递的影响。8-OH-DPAT显著抑制单突触传递诱发的α运动神经元兴奋,而对α运动神经元兴奋无直接影响。DOI通过直接刺激和单突触传递增强α运动神经元的兴奋。这些结果表明,5-羟色胺1A受体的激活抑制单突触传递,而5-羟色胺2A/2C受体的激活则增强单突触传递。