Glaum S R, Brooks P A, Spyer K M, Miller R J
Department of Pharmacological and Physiological Sciences, University of Chicago, IL 60637.
Brain Res. 1992 Aug 28;589(1):62-8. doi: 10.1016/0006-8993(92)91162-8.
Whole-cell patch clamp recordings were made from neurons in the rat nucleus tractus solitarius (NTS) in transverse brainstem slices. 5-Hydroxytryptamine (5-HT, 100 microM) and the selective 5-HT3 receptor agonist 2-methyl-5-HT (2-CH3-5-HT, 100 microM) depolarized 86% of NTS neurons at resting membrane potential (Vm). This response was resistant to tetrodotoxin (TTX) and Co2+ application. In addition, 2-CH3-5-HT (500 nM-100 microM) increased the amplitude and frequency of both excitatory and inhibitory spontaneous synaptic potentials. This effect was also TTX-resistant, but was abolished by Co2+. The effects of 2-CH3-5-HT on EPSPs and IPSPs evoked by electrical stimulation of the tractus solitarius (TS) were analyzed separately in the presence of bicuculline or 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), respectively. Concentrations of 2-CH3-5-HT between 500 nM and 1 microM decreased the amplitude of evoked EPSPs and IPSPs with similar potency. The selective 5-HT3 receptor antagonists ICS 205-930 (10 nM) and MDL 72222 (10 microM) reversibly blocked the effects of 2-CH3-5-HT at all doses examined. It is concluded that 5-HT3 receptors can mediate both pre- and postsynaptic responses in the NTS.
在横断脑干切片中,对大鼠孤束核(NTS)中的神经元进行全细胞膜片钳记录。5-羟色胺(5-HT,100微摩尔)和选择性5-HT3受体激动剂2-甲基-5-HT(2-CH3-5-HT,100微摩尔)使86%处于静息膜电位(Vm)的NTS神经元发生去极化。该反应对河豚毒素(TTX)和Co2+的应用具有抗性。此外,2-CH3-5-HT(500纳摩尔-100微摩尔)增加了兴奋性和抑制性自发突触电位的幅度和频率。这种效应也对TTX具有抗性,但被Co2+消除。分别在荷包牡丹碱或6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)存在的情况下,分析了2-CH3-5-HT对孤束(TS)电刺激诱发的兴奋性突触后电位(EPSP)和抑制性突触后电位(IPSP)的影响。500纳摩尔至1微摩尔之间的2-CH3-5-HT浓度以相似的效力降低了诱发的EPSP和IPSP的幅度。选择性5-HT3受体拮抗剂ICS 205-930(10纳摩尔)和MDL 72222(10微摩尔)在所有检测剂量下均可逆地阻断了2-CH3-5-HT的作用。得出的结论是,5-HT3受体可介导NTS中的突触前和突触后反应。