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人类I组脊髓各通路中的激活后抑制

Post-activation depression in various group I spinal pathways in humans.

作者信息

Lamy J C, Wargon I, Baret M, Ben Smail D, Milani P, Raoul S, Pénicaud A, Katz R

机构信息

U731 INSERM/UPMC, Service de Médecine Physique et Réadaptation CHU Pitié-Salpêtrière, 75651 Paris cedex 13, France.

出版信息

Exp Brain Res. 2005 Oct;166(2):248-62. doi: 10.1007/s00221-005-2360-4. Epub 2005 Aug 3.

Abstract

This investigation was designed to study the effects of post-activation depression in different spinal pathways fed by group I afferents available to investigation in human subjects. It was precipitated by a recent investigation in the cat showing that-contrary to the general assumption-post-activation depression is not a widespread phenomenon in the spinal cord. In 24 healthy subjects comparison was made between the effects of low and high-test stimulus rates on the monosynaptic Ia excitation, known to be subject to post-activation depression, and on oligosynaptic pathways fed by group I afferents. Both the amplitude of monosynaptic H reflexes and the amount of heteronymous monosynaptic Ia facilitation were significantly smaller at high than at low-test stimulus rates (1-2 s compared with 6-8 s between two consecutive stimuli). So was the amount of reciprocal Ia inhibition of tibialis anterior motoneurones. In contrast, the amount of other non-monosynaptic group I effects directed to the same motor nuclei (peroneal-induced excitation of quadriceps motoneurones, disynaptic non-reciprocal group I inhibition of flexor carpi radialis motoneurones, and D1 inhibition of flexor carpi radialis and soleus H reflexes) were enhanced at high stimulus rates. Results in humans confirm that post-activation depression depends on the type of group I afferents, and/or on the target neurones. The functional significance of the discrepancy between post-activation depression in pure Ia pathways and in other group I pathways is discussed with regard to the fusimotor-driven servo-assistance from Ia afferent discharges.

摘要

本研究旨在探讨在人类受试者中可进行研究的、由I类传入纤维支配的不同脊髓通路中,激活后抑郁的影响。这是由最近一项对猫的研究引发的,该研究表明,与一般假设相反,激活后抑郁在脊髓中并非普遍现象。在24名健康受试者中,比较了低测试刺激率和高测试刺激率对单突触Ia兴奋(已知易受激活后抑郁影响)以及对由I类传入纤维支配的多突触通路的影响。高测试刺激率下(连续两次刺激之间为1 - 2秒,而低测试刺激率为6 - 8秒),单突触H反射的幅度和异源单突触Ia易化量均显著低于低测试刺激率时的水平。胫前运动神经元的Ia交互抑制量也是如此。相比之下,针对相同运动核的其他非单突触I类效应的量(腓总神经诱发的股四头肌运动神经元兴奋、桡侧腕屈肌运动神经元的双突触非交互I类抑制以及桡侧腕屈肌和比目鱼肌H反射的D1抑制)在高刺激率下增强。人类的研究结果证实,激活后抑郁取决于I类传入纤维的类型和/或靶神经元。本文还就Ia传入放电的肌梭运动驱动伺服辅助作用,讨论了纯Ia通路和其他I类通路中激活后抑郁差异的功能意义。

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