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猫后肢Ⅲ类肌肉传入纤维电刺激对γ运动神经元的作用。

Actions on gamma-motoneurones elicited by electrical stimulation of group III muscle afferent fibres in the hind limb of the cat.

作者信息

Appelberg B, Hulliger M, Johansson H, Sojka P

出版信息

J Physiol. 1983 Feb;335:275-92. doi: 10.1113/jphysiol.1983.sp014533.

Abstract

The reflex actions evoked by electrical stimulation of group III muscle afferent fibres were investigated with micro-electrode recordings from ninety-three gamma-motoneurones projecting to hind-limb muscles of cats anaesthetized with chloralose. For seventy-eight of the ninety-three gamma-cells the frequency of occurrence and types of effects mediated via group II and group III muscle fibres were compared. Seventy-seven of the cells tested at intensities which excited group III and seventy-five of the cells tested at intensities which excited both group II and group III afferent fibres were classified as either static or dynamic, using the method of mesencephalic stimulation (Appelberg, 1981). The responsiveness of the whole sample of gamma-motoneurones to inputs from group III muscle fibres was high and comparable to that found with group II fibres. It was found that group III muscle fibres acted preferentially on static gamma-motoneurones. In contrast, group II fibres acted preferentially on dynamic gamma-motoneurones. Both excitatory and inhibitory effects were provoked by stimulation of group III fibres. Generally excitation was more frequent than inhibition. A strong dominance of excitation over inhibition was found in flexor muscles, and a weaker prevalence of excitation was also encountered in extensor muscles. This prevalence of excitation in extensor gamma-motoneurones is in contrast to the striking predominance of group III-evoked inhibition of extensor alpha-motoneurones as described by the flexion reflex afferents concept. A comparative survey is also given of the patterns of responses elicited in individual posterior biceps-semitendinosus and gastrocnemius-soleus gamma-cells by stimulation of group II and group III fibres. These data further corroborate the view that reflexes from high-threshold muscle afferent fibres to gamma-motoneurones are organized differently from those to alpha-motoneurones. The functional implications of these findings are discussed. It is proposed that the pools of gamma-motoneurones should be considered as integrative systems intercalated between descending and reflex pathways on the one hand and the skeletomotor neurones on the other. The descending messages and the multisensory peripheral information, integrated in the fusimotor neurones, undergo final adjustment in the muscle spindle. The link to the skeletomotor neurones is formed by the primary spindle afferents. These constitute a final common input, conveying integrated detailed polymodal feed-back, to the central nervous system. This new concept is referred to as the 'final common input' hypothesis.

摘要

采用微电极记录技术,对93个投射至用氯醛糖麻醉的猫后肢肌肉的γ运动神经元进行研究,以探究电刺激Ⅲ类肌传入纤维所诱发的反射活动。在这93个γ细胞中,对其中78个细胞比较了经由Ⅱ类和Ⅲ类肌纤维介导的效应的发生频率和类型。使用中脑刺激方法(阿佩尔贝里,1981年),在能兴奋Ⅲ类纤维的强度下对77个细胞进行测试,在能同时兴奋Ⅱ类和Ⅲ类传入纤维的强度下对75个细胞进行测试,并将这些细胞分为静态或动态两类。γ运动神经元全样本对Ⅲ类肌纤维输入的反应性很高,与对Ⅱ类纤维的反应性相当。研究发现,Ⅲ类肌纤维优先作用于静态γ运动神经元。相比之下,Ⅱ类纤维优先作用于动态γ运动神经元。刺激Ⅲ类纤维可引发兴奋和抑制两种效应。一般来说,兴奋比抑制更频繁。在屈肌中发现兴奋对抑制有很强的优势,在伸肌中也遇到兴奋的较弱优势。伸肌γ运动神经元中这种兴奋的优势与屈肌反射传入概念所描述的Ⅲ类诱发的伸肌α运动神经元抑制的显著优势形成对比。还对刺激Ⅱ类和Ⅲ类纤维在单个后二头肌 - 半腱肌和腓肠肌 - 比目鱼肌γ细胞中引发的反应模式进行了比较研究。这些数据进一步证实了这样一种观点,即从高阈值肌传入纤维到γ运动神经元的反射与到α运动神经元反射的组织方式不同。讨论了这些发现的功能意义。有人提出,γ运动神经元池应被视为一方面介于下行和反射通路与另一方面的骨骼肌运动神经元之间的整合系统。下行信息和多感觉外周信息在梭内运动神经元中整合,在肌梭中进行最终调整。与骨骼肌运动神经元的联系由初级肌梭传入纤维形成。这些构成了最终的共同输入,向中枢神经系统传递整合的详细多模式反馈。这个新概念被称为“最终共同输入”假说。

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本文引用的文献

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Supraspinal control of the muscle spindles and its significance.肌梭的脊髓上控制及其意义。
J Physiol. 1953 Dec 29;122(3):498-523. doi: 10.1113/jphysiol.1953.sp005017.
8
Descending monosynaptic and reflex control of gamma-motoneurones.γ运动神经元的下行单突触和反射控制
Acta Physiol Scand. 1969 Apr;75(4):592-613. doi: 10.1111/j.1748-1716.1969.tb04414.x.
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Comments on reflex actions evoked by electrical stimulation of group II muscle afferents.
Brain Res. 1977 Feb 25;122(3):551-5. doi: 10.1016/0006-8993(77)90466-8.

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