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全身麻醉剂对青蛙离体脊髓根部反应的作用。

The action of general anaesthetic agents on root responses of the frog isolated spinal cord.

作者信息

Richens A

出版信息

Br J Pharmacol. 1969 Jun;36(2):294-311. doi: 10.1111/j.1476-5381.1969.tb09507.x.

Abstract
  1. The action of volatile and barbiturate general anaesthetic agents on synaptic transmission in the frog isolated spinal cord has been studied by recording ventral root synaptic potentials and spike discharges evoked by volleys in a dorsal root and in the lateral column fibres.2. Some observations on the distribution of the lateral column fibres and the characteristics of the dorsal root potentials have been presented.3. Volatile agents depressed and eventually abolished all components of the ventral root responses. Failure of motoneurone discharge was the result of two factors, a decrease in the slope of the synaptic potential and an elevation of the critical depolarization required to trigger propagated impulses.4. Barbiturate compounds, in contrast, readily abolished polysynaptic components of the ventral root responses, but the short latency discharge produced by lateral column stimulation was potentiated, and was accompanied by a lowering of the firing threshold of motoneurones. The mechanism of this potentiation by barbiturate compounds is discussed.5. It is concluded that volatile agents act predominantly on the initial segment and subsynaptic elements of the motoneurone, whereas barbiturate compounds depress the presynaptic or postsynaptic components of interneuronal synapses.
摘要
  1. 通过记录由背根和外侧柱纤维的电刺激串诱发的腹根突触电位和动作电位发放,研究了挥发性和巴比妥类全身麻醉药对离体蛙脊髓突触传递的作用。

  2. 已对外侧柱纤维的分布和背根电位的特征进行了一些观察。

  3. 挥发性药物抑制并最终消除了腹根反应的所有成分。运动神经元发放失败是两个因素的结果,即突触电位斜率的降低和触发动作电位所需的临界去极化的升高。

  4. 相比之下,巴比妥类化合物很容易消除腹根反应的多突触成分,但外侧柱刺激产生的短潜伏期发放增强,并且伴有运动神经元发放阈值的降低。讨论了巴比妥类化合物这种增强作用的机制。

  5. 得出的结论是,挥发性药物主要作用于运动神经元的起始段和突触下成分,而巴比妥类化合物则抑制中间神经元突触的突触前或突触后成分。

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本文引用的文献

1
The interpretation of potential changes in the spinal cord.脊髓潜在变化的解读。
J Physiol. 1938 Apr 14;92(3):276-321. doi: 10.1113/jphysiol.1938.sp003603.
2
Motor mechanisms of the anuran brain.
J Comp Neurol. 1950 Jun;92(3):241-91. doi: 10.1002/cne.900920302.
3
[Synaptic potentials and central nervous system transmission].[突触电位与中枢神经系统传递]
Arch Int Physiol. 1952 Feb;60(1):33-93. doi: 10.3109/13813455209145032.
6
PHARMACOLOGICAL STUDIES ON PRESYNAPTIC INHIBITION.突触前抑制的药理学研究
J Physiol. 1963 Oct;168(3):500-30. doi: 10.1113/jphysiol.1963.sp007205.
8
PHARMACOLOGICAL STUDIES ON THE PRIMARY AFFERENT DEPOLARIZATION OF THE TOAD SPINAL CORD.蟾蜍脊髓初级传入去极化的药理学研究
Pflugers Arch Gesamte Physiol Menschen Tiere. 1963 Jul 2;277:325-46. doi: 10.1007/BF00362515.

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