Wang D S, Xu T L, Pang Z P, Li J S
Department of Anatomy and K.K. Leung Brain Research Centre, Fourth Military Medical University, Xi'an 710032.
Sheng Li Xue Bao. 1998 Dec;50(6):656-62.
Using nystatin-perforated whole-cell recording configuration, the modulatory effect of serotonin (5-hydroxytryptamine, 5-HT) on taurine (Tau)-activated current (ITau) was investigated in neurons dissociated from the rat sacral dorsal commissural nucleus (SDCN). The results are as follows: (1) Tau acted on strychnine-sensitive glycine (Gly) receptors and elicited inward currents at a holding potential (VH) of -40 mV in SDCN neurons; (2)in a range of 0.01 to 100 mumol/L, 5-HT enhanced ITau in a concentration-dependent manner; (3) both the reversal potential of Tau and the binding affinity of Tau to Gly receptor were not affected by 5-HT; (4) when the neurons were loaded with 3 mumol/L chelerythrine, application of 1 mumol/L 5-HT failed to enhance ITau. The above results thus indicate that intracellular PKC pathway is at least partially involved in the enhancement of ITau by 5-HT. In accordance with our previous study, it is suggested that 5-HT may play an important antinociceptive function in SDCN through enhanced Gly and Tau inhibitory effects.
采用制霉菌素穿孔全细胞记录模式,在从大鼠骶髓后连合核(SDCN)分离的神经元中研究了5-羟色胺(5-HT)对牛磺酸(Tau)激活电流(ITau)的调制作用。结果如下:(1)Tau作用于士的宁敏感的甘氨酸(Gly)受体,并在SDCN神经元-40 mV的钳制电位(VH)下引发内向电流;(2)在0.01至100 μmol/L范围内,5-HT以浓度依赖的方式增强ITau;(3)Tau的反转电位和Tau与Gly受体的结合亲和力均不受5-HT影响;(4)当神经元用3 μmol/L白屈菜红碱处理后,施加1 μmol/L 5-HT不能增强ITau。上述结果表明,细胞内PKC途径至少部分参与了5-HT对ITau的增强作用。与我们之前的研究一致,提示5-HT可能通过增强Gly和Tau的抑制作用在SDCN中发挥重要的抗伤害感受功能。