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振动长期作用过程中网状结构与边缘系统相互关系的电生理研究

Electrophysiological study of reticulo-limbic interrelationships during prolonged action of vibration.

作者信息

Minasyan S M, Baklavadzhyan O G

机构信息

Department of Human and Animal Physiology, State University, Erevan.

出版信息

Neurosci Behav Physiol. 1987 Nov-Dec;17(6):531-8. doi: 10.1007/BF01186354.

DOI:10.1007/BF01186354
PMID:3441286
Abstract

Phasic changes in the bioelectrical activity of the dorsal hippocampus (field CA3), the mesencephalic reticular formation, and several regions of the neocortex and the reticulo-cortical evoked potentials were measured under conditions of the action of prolonged vibration (3 months) in electrophysiological experiments with rabbits. Daily three-hour vibration during the first month of the experiment evoked an activation reaction in the EEG, characterized by a desynchronization effect in the neocortex and hippocampus and by the stabilization of the v rhythm in the mesencephalic reticular formation. Noted against this background was a certain facilitation in the reticulo-cortical evoked potentials, more pronounced in the neocortex, and a decline in the ascending activational influence of the mesencephalic reticular formation. The three-month action of vibration exerted an inhibitory influence on reticulo-cortical interrelationships, expressed in a decline in the compound bioelectrical activity of the cortex and subcortical formations, the excitability of the mesencephalic reticular formation, and the suppression of reticulo-cortical evoked potentials. At the same time an elongation of the latent periods of the positive phases of the evoked potentials, a decline in their amplitude, and a reduction of the negative phase in limbic structures was noted. The question of the physiological mechanism of development of vibrational pathology is discussed.

摘要

在对家兔进行的电生理实验中,在长时间振动(3个月)作用的条件下,测量了背侧海马体(CA3区)、中脑网状结构、新皮质的几个区域以及网状结构 - 皮质诱发电位的生物电活动的阶段性变化。在实验的第一个月,每天3小时的振动在脑电图中引发了一种激活反应,其特征是新皮质和海马体出现去同步化效应,中脑网状结构的v节律稳定。在此背景下,网状结构 - 皮质诱发电位有一定程度的易化,在新皮质中更为明显,同时中脑网状结构的上行激活影响下降。振动3个月的作用对网状结构 - 皮质的相互关系产生了抑制作用,表现为皮质和皮质下结构的复合生物电活动下降、中脑网状结构的兴奋性下降以及网状结构 - 皮质诱发电位的抑制。同时,观察到诱发电位正相潜伏期延长、幅度下降以及边缘结构中负相减小。文中讨论了振动性病理发展的生理机制问题。

相似文献

1
Electrophysiological study of reticulo-limbic interrelationships during prolonged action of vibration.振动长期作用过程中网状结构与边缘系统相互关系的电生理研究
Neurosci Behav Physiol. 1987 Nov-Dec;17(6):531-8. doi: 10.1007/BF01186354.
2
[Electrophysiologic study of reticulo-limbic relations during long-term exposure to vibration].[长期暴露于振动过程中网状结构与边缘系统关系的电生理研究]
Fiziol Zh SSSR Im I M Sechenova. 1987 Jan;73(1):20-7.
3
[Dependence of the spectrum of electrical activity of the neocortex and hippocampus in rabbits on the intensity of the stimulation of the midbrain reticular formation].[家兔新皮层和海马电活动频谱对中脑网状结构刺激强度的依赖性]
Zh Vyssh Nerv Deiat Im I P Pavlova. 1988 Mar-Apr;38(2):313-22.
4
[Neuronal mechanisms of reticulocortical activation].[网状皮质激活的神经元机制]
Zh Vyssh Nerv Deiat Im I P Pavlova. 1981 Jan-Feb;31(1):129-39.
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Zh Vyssh Nerv Deiat Im I P Pavlova. 1975 Sep-Oct;25(5):1076-82.
6
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Zh Vyssh Nerv Deiat Im I P Pavlova. 1994 Nov-Dec;44(6):1038-45.
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[Evoked responses and impulse activity of the neocortex during the startle response following stimulation of the midbrain reticular formation].
Zh Vyssh Nerv Deiat Im I P Pavlova. 1980 Jan-Feb;30(1):97-104.
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Increased regularity of activity of cortical neurons in learning due to disinhibitory effect of reinforcement.由于强化的去抑制作用,学习过程中皮层神经元活动的规律性增加。
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本文引用的文献

1
EEG records from cortical and deep brain structures during centrifugal and vibrational accelerations in cats and monkeys.猫和猴子在离心和振动加速过程中皮层及深部脑结构的脑电图记录。
Ire Trans Biomed Electron. 1961 Jul;8:182-8. doi: 10.1109/tbmel.1961.4322895.
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The rabbit diencephalon in stereotaxic coordinates.立体定位坐标下的兔间脑。
J Comp Neurol. 1954 Dec;101(3):801-24. doi: 10.1002/cne.901010307.
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Hippocampal electrical activity in arousal.觉醒状态下的海马体电活动。
J Neurophysiol. 1954 Nov;17(6):533-57. doi: 10.1152/jn.1954.17.6.533.
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Drug action on the electrical activity of the hippocampus.药物对海马体电活动的作用。
Int Rev Neurobiol. 1965;8:77-138. doi: 10.1016/s0074-7742(08)60756-4.