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巴比妥酸盐引起豚鼠嗅皮质切片中抑制电位增强。

A barbiturate induced intensification of the inhibitory potential in slices of guinea-pig olfactory cortex.

作者信息

Scholfield C N

出版信息

J Physiol. 1978 Feb;275:559-66. doi: 10.1113/jphysiol.1978.sp012208.

Abstract
  1. A study has been made of the effect of barbiturates on membrane constants and synaptic potentials of neurones in the isolated guinea-pig olfactory cortex slice. 2. Normally, a long depolarizing i.p.s.p. follows the e.p.s.p. Pentobarbitone (0.1 mM) produced a tenfold increase in the duration of the high conductance phase of this i.p.s.p. 3. The i.p.s.p. was potentiated increasingly with higher barbiturate concentrations from 0.02 to 1.0 mM-pentobarbitone and 0.2 to 5 mM-phenobarbitone. 4. The resting membrane conductance, the initial phase of the e.p.s.p. and the threshold for the action potential were unaffected at lower concentrations. 5. The highest barbiturate doses increased the resting membrane conductance. This was associated with a depolarization of about 14 mV maximally and resulted in smaller synaptic potentials. The effect was probably generated by the same mechanism as the i.p.s.p. 6. This fortifies the idea that barbiturates have a primary action on prolonging inhibition rather than a depression in the excitatory potential.
摘要
  1. 已经对巴比妥类药物对豚鼠离体嗅皮层切片中神经元的膜常数和突触电位的影响进行了研究。2. 正常情况下,在兴奋性突触后电位(e.p.s.p.)之后会出现一个长时程的去极化抑制性突触后电位(i.p.s.p.)。戊巴比妥(0.1 mM)使该i.p.s.p.的高电导阶段的持续时间增加了十倍。3. 随着巴比妥类药物浓度升高,从0.02至1.0 mM的戊巴比妥和0.2至5 mM的苯巴比妥,i.p.s.p.的增强作用越来越明显。4. 在较低浓度下,静息膜电导、e.p.s.p.的初始阶段以及动作电位的阈值均未受影响。5. 最高剂量的巴比妥类药物增加了静息膜电导。这与最大约14 mV的去极化相关,并导致较小的突触电位。这种效应可能是由与i.p.s.p.相同的机制产生的。6. 这强化了这样一种观点,即巴比妥类药物的主要作用是延长抑制作用,而不是抑制兴奋性电位。

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PHARMACOLOGICAL STUDIES ON PRESYNAPTIC INHIBITION.突触前抑制的药理学研究
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