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Correlation of the inhibitory post-synaptic potential of motoneurones with the latency and time course of inhibition of monosynaptic reflexes.运动神经元抑制性突触后电位与单突触反射抑制的潜伏期和时程的相关性。
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The afferent volleys responsible for spinal proprioceptive reflexes in man.负责人类脊髓本体感受反射的传入冲动。
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Spinal inhibition in man: depression of the soleus H reflex by stimulation of the nerve to the antagonist muscle.人类的脊髓抑制:通过刺激拮抗肌的神经来抑制比目鱼肌的H反射。
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Pathophysiology of dystonias.肌张力障碍的病理生理学
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Transmission in the spinal reciprocal Ia inhibitory pathway preceding willed movements of the human wrist.人类手腕自主运动之前脊髓交互性Ia抑制通路中的信号传导。
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Reflex effects of muscle afferents on antagonist studied on single firing motor units in man.在人体单个放电运动单位上研究肌肉传入神经对拮抗剂的反射作用。
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Synaptic actions of single interneurones mediating reciprocal Ia inhibition of motoneurones.介导运动神经元相互 Ia 抑制的单个中间神经元的突触作用。
J Physiol. 1972 May;222(3):623-42. doi: 10.1113/jphysiol.1972.sp009818.
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Reciprocal Ia inhibition during voluntary movements in man.人类随意运动期间的交互性Ia抑制。
Exp Brain Res. 1974;21(5):529-40. doi: 10.1007/BF00237171.
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Reciprocal group I inhibition on triceps surae motoneurons in man.人类小腿三头肌运动神经元的交互性I组抑制
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10
Transmission of corticospinal IPSPs to cat forelimb motoneurones via high cervical propriospinal neurones and La inhibitory interneurones.皮质脊髓抑制性突触后电位通过高颈段脊髓固有神经元和拉什曼抑制性中间神经元向猫前肢运动神经元的传递。
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人类前臂肌肉之间的交互抑制。

Reciprocal inhibition between the muscles of the human forearm.

作者信息

Day B L, Marsden C D, Obeso J A, Rothwell J C

出版信息

J Physiol. 1984 Apr;349:519-34. doi: 10.1113/jphysiol.1984.sp015171.

DOI:10.1113/jphysiol.1984.sp015171
PMID:6737302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1199352/
Abstract

Peripheral and central mechanisms of reciprocal inhibition between antagonist muscles in the forearm have been studied in ten human subjects. H reflexes were evoked in flexor muscles by stimulating the median nerve with single shocks at around motor threshold intensity. Peripheral inhibition of the flexor H reflex was produced by motor threshold stimulation with a single shock of the radial nerve supplying the extensor muscles. The conditioning radial nerve stimulus produced inhibition of the flexor H reflex consisting of three phases. In some individuals, an H reflex could be evoked in extensor muscles of the forearm. Stimulation of the median nerve produced inhibition of the extensor H reflex with a similar time course to that from extensors to flexors. The first phase of inhibition was apparent when the test median nerve shock was given from 1 ms before to 3 ms after the conditioning radial nerve shock. It was abrupt in onset and short in duration and could be evoked with a conditioning stimulus intensity as low as 0.75 X motor threshold. The second and third phases of inhibition were evident when the conditioning radial nerve stimulus preceded the median nerve test shock by 5 to 50, and 50 to 500 ms respectively. The characteristics of these later phases of inhibition are to be the subject of a separate report. The difference in timing of the peak initial short-latency inhibition from extensor to flexor and from flexor to extensor muscles enabled an estimate to be made of the central synaptic delay of the inhibitory process. This method yielded a central delay of 0.95 ms in excess of that of the H reflex. We conclude that the first phase of inhibition is mediated via large group I afferents acting through a single inhibitory interneurone . Central inhibition of the flexor H reflex was demonstrated with the radial nerve anaesthetized by injection of local anaesthetic at the elbow. Subjects were asked to try to contract the paralysed extensor muscles. Under this condition, attempted voluntary wrist extension inhibited the flexor H reflex even though no movement occurred. A shock was delivered to the radial nerve at a site proximal to the anaesthetic block. When the shock was applied in conjunction with an attempted voluntary contraction of the paralysed extensor muscles, the depth of inhibition was greater than that predicted from the effect of either a shock or a willed contraction acting independently.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

对10名受试者的前臂拮抗肌之间交互抑制的外周和中枢机制进行了研究。通过在运动阈值强度附近用单次电刺激正中神经来诱发屈肌中的H反射。用单次电刺激支配伸肌的桡神经进行运动阈值刺激,从而产生屈肌H反射的外周抑制。条件性桡神经刺激产生的屈肌H反射抑制包括三个阶段。在一些个体中,可在前臂伸肌中诱发H反射。刺激正中神经对伸肌H反射产生抑制,其时间进程与从伸肌到屈肌的抑制相似。当测试正中神经电刺激在条件性桡神经电刺激前1毫秒至后3毫秒给予时,第一阶段的抑制很明显。其起始突然,持续时间短,且可由低至0.75倍运动阈值的条件刺激强度诱发。当条件性桡神经刺激分别先于正中神经测试电刺激5至50毫秒和50至500毫秒时,第二和第三阶段的抑制明显。这些后期抑制阶段的特征将在另一篇报告中阐述。从伸肌到屈肌以及从屈肌到伸肌的初始短潜伏期抑制峰值在时间上的差异,使得能够对抑制过程的中枢突触延迟进行估计。该方法得出的中枢延迟比H反射的中枢延迟长0.95毫秒。我们得出结论,第一阶段的抑制是通过经由单个抑制性中间神经元起作用的大的I类传入纤维介导的。通过在肘部注射局部麻醉剂使桡神经麻醉,证明了屈肌H反射的中枢抑制。要求受试者尝试收缩麻痹的伸肌。在这种情况下,尽管没有运动发生,但试图进行的自愿性腕部伸展抑制了屈肌H反射。在麻醉阻滞近端的部位对桡神经进行电刺激。当该电刺激与试图对麻痹的伸肌进行自愿收缩同时施加时,抑制深度大于单独的电刺激或意志收缩所产生效应的预测值。(摘要截短于400字)