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5-HT3 receptor channels in dissociated rat superior cervical ganglion neurons.

机译:离体大鼠上颈神经节神经元中的5-HT 3受体通道。

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摘要

1. Whole-cell and single-channel voltage-clamp techniques were used to record the 5-HT3 receptor-mediated currents in neurons freshly dissociated from rat superior cervical ganglia. 2. Whole-cell currents elicited by brief pressure ejection of 5-HT (10 microM) reversed at -4.5 mV when extracellular and intracellular solutions mainly contained NaCl and CsCl. The peak current-voltage relation showed modest inward rectification that was fully developed within less than 2 ms of the applied voltage step. 3. With prolonged application of 5-HT (10 microM) using a fast perfusion system, the response desensitized in two phases with fast and slow time constants of 0.57 and 6.0 s at -74 mV. The time constants showed little voltage dependence; however, the relative amplitude of the two components was significantly dependent on voltage. The time course of desensitization was not affected by agents that increase the levels of intracellular cyclic AMP. 4. The relative permeability of the channel was determined from reversal potential changes. The channel passed small cations non-selectively, with permeability ratios (PX/PNa) of 0.93 and 1.24 for Cs+ and K+. The organic cations Tris and glucosamine were measurably permeant with permeability ratios of 0.19 and 0.06. Ca2+ was fairly permeant with a relative permeability of 0.55 in 20 mM solution and of 0.16 when the concentration of CaCl2 was increased to 115 mM. No permeability was detected for Cl-. 5. Fluctuation analysis of the whole-cell current revealed an apparent single-channel current of approximately 0.18 pA at -74 mV. 6. 5-HT-activated single-channel currents were recorded in excised outside-out patches. When 5-HT (10 microM) was delivered by pressure ejection, channel openings appeared rapidly with a delay of 28 ms. The unitary current was about approximately 0.80 pA at -74 mV. The channel activity induced by bath perfusion of 5-HT (0.8 microM) was significantly reduced by 100 nM of the 5-HT3 receptor-specific antagonists 3-tropanyl-3,5-dichlorobenzoate (MDL 72222) or 3-tropanyl-indole-3-carboxylate (ICS 205-930). 7. The single-channel current-voltage relation was non-linear, with moderate inward rectification similar to that of the whole-cell current. The chord conductance of the channel decreased with membrane depolarization from 14.6 pS at -104 mV to only 9.9 pS at -54 mV. Open-time distributions consisted of two components with mean time constants of 0.45 and 2.8 ms at -104 mV. Burst-length distributions were also made up of two components with time constants of 0.45 and 4.6 ms.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.使用全细胞和单通道电压钳技术记录从大鼠上颈神经节新鲜分离的神经元中5-HT3受体介导的电流。 2.当细胞外和细胞内溶液主要含有NaCl和CsCl时,由5-HT(10 microM)的短暂压力喷射引起的全细胞电流在-4.5 mV时反转。峰值电流-电压关系显示出适度的内向整流,该内向整流在所施加电压阶跃的不到2 ms内完全显现。 3.通过使用快速灌注系统长时间使用5-HT(10 microM),在-74 mV时,快速和慢速时间常数分别为0.57和6.0 s的两个阶段使响应减敏。时间常数几乎没有电压依赖性。但是,这两个分量的相对幅度明显取决于电压。脱敏的时间过程不受增加细胞内环状AMP水平的药物的影响。 4.通道的相对磁导率由反向电位变化确定。通道非选择性地通过小阳离子,对于Cs +和K +,渗透率比(PX / PNa)为0.93和1.24。有机阳离子Tris和氨基葡萄糖可测量地渗透,渗透率分别为0.19和0.06。 Ca2 +相当渗透,在20 mM溶液中的相对渗透率为0.55,而当CaCl2的浓度增加到115 mM时的相对渗透率为0.16。没有检测到Cl-的渗透性。 5.全电池电流的波动分析显示,在-74 mV时,表观单通道电流约为0.18 pA。 6.将5-HT激活的单通道电流记录在切除的外露斑块中。通过压力喷射输送5-HT(10 microM)时,通道开口迅速出现,延迟28 ms。在-74 mV时,单位电流约为0.80 pA。 100 nM 5-HT3受体特异性拮抗剂3-tropanyl-3,5-dichlorobenzoate(MDL 72222)或3-tropanyl-吲哚-100-M可以显着降低5-HT(0.8 microM)的浴灌注诱导的通道活性。 3-羧酸盐(ICS 205-930)。 7.单通道电流-电压关系是非线性的,具有适度的向内整流,类似于全电池电流。随着膜的去极化,通道的弦电导从-104 mV的14.6 pS降低到-54 mV的9.9 pS。开放时间分布包括两个成分,在-104 mV时的平均时间常数为0.45和2.8 ms。突发长度分布还由两个时间常数分别为0.45和4.6 ms的分量组成(抽象截断为400字)

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