首页> 外文期刊>The Journal of Physiology >Kinetic analysis of voltage-dependent potentiation and block of the glycine alpha 3 receptor by a neuroactive steroid analogue.
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Kinetic analysis of voltage-dependent potentiation and block of the glycine alpha 3 receptor by a neuroactive steroid analogue.

机译:对神经活性类固醇类似物的电压依赖性增强和甘氨酸α3受体阻滞的动力学分析。

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We examined the actions of a carboxylated analogue of pregnanolone ((3alpha,5beta)-20-oxopregnane-3-carboxylic acid; 3alphaCOOH5betaP) on receptors composed of glycine receptor alpha3 subunits, expressed in Xenopus oocytes. This analogue both inhibits and potentiates this receptor; potentiation increases with more negative membrane potentials while block increases with less negative membrane potentials. We used a second analogue ((3alpha,5beta)-3-hydroxymethylpregnan-20-one; 3alphaCH(2)OH5betaP) to examine the mechanism for voltage-dependent potentiation. This analogue potentiates but does not block the glycine alpha3 receptor. Steady-state responses and current relaxations following voltage jumps support the idea that the voltage dependence of potentiation indirectly arises from a voltage dependence for channel activation by glycine, rather than an intrinsic voltage dependence for potentiation. Potentiation results from a slowing of the channel deactivation rate. In the absence of steroid, at a low [glycine] current relaxations after a voltage jump show two exponential components, with a weighted average time constant of approximately 425 ms (-50 mV, 22 degrees C). The rate for channel deactivation increases at more negative potentials (e-fold per 170 mV) whereas activation decreases (e-fold per 230 mV). The probability a channel is active at a high [glycine] is greater than 0.9. The addition of 10 microM 3alphaCH(2)OH5betaP decreases the deactivation rate by 6.3-fold (-50 mV). Voltage-dependent block by 3alphaCOOH5betaP is consistent with simple open-channel block, with voltage dependence reflecting interactions of the charge on the analogue with the electrical field. Block and unblock have equal but opposite dependence on membrane potential, and the charge on 3alphaCOOH5betaP senses approximately 70% of the membrane field at the blocking site. The apparent forward rate for block, however, is very slow (2 x 10(5) m(-1) s(-1)).
机译:我们检查了孕烯醇酮的羧化类似物((3α,5β)-20-氧杂戊烷-3-羧酸;3αCOOH5βP)对非洲爪蟾卵母细胞中表达的甘氨酸受体α3亚基受体的作用。该类似物既抑制又增强了该受体。负膜电位越高,电位增强作用越强,而负膜电位越低,阻滞作用增强。我们使用了第二个类似物((3alpha,5beta)-3-hydroxymethylpregnan-20-one; 3alphaCH(2)OH5betaP)检查电压依赖性增强的机制。该类似物增强但不阻断甘氨酸α3受体。电压跃变后的稳态响应和电流松弛支持这样的想法,即电位的电压依赖性间接源于甘氨酸激活通道的电压依赖性,而不是电位的固有电压依赖性。增强作用是由通道失活速率减慢导致的。在没有类固醇的情况下,在低[甘氨酸]电流时,电压跃变后的弛豫表现出两个指数成分,加权平均时间常数约为425毫秒(-50 mV,22摄氏度)。通道失活的速率在更多的负电势下增加(每170 mV e倍),而激活降低(每230 mV的e倍)。通道在高[甘氨酸]时处于活动状态的概率大于0.9。 10 microM 3alphaCH(2)OH5betaP的添加使失活速率降低6.3倍(-50 mV)。 3alphaCOOH5betaP的电压依赖性阻断与简单的开放通道阻断相一致,电压依赖性反映了模拟物上电荷与电场的相互作用。阻滞和解阻对膜电位的依赖性相同但相反,并且3alphaCOOH5betaP上的电荷感测了阻滞位点约70%的膜场。但是,块的视在正向速率非常慢(2 x 10(5)m(-1)s(-1))。

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