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麻醉猫大脑诱发电位的长潜伏期成分。

The long-latency component of cerebral evoked potentials in anesthetized cats.

作者信息

Lee K H, Kim J, Chung J M

出版信息

J Neurosurg. 1986 Sep;65(3):392-7. doi: 10.3171/jns.1986.65.3.0392.

Abstract

A late component of the cortical evoked potential elicited by somatosensory afferent input was studied in cats anesthetized with alpha-chloralose. Cortical evoked potentials were recorded from the somatosensory-motor cortex during stimulation of the sural nerve with graded intensities. The stimulus intensity was adjusted to activate A alpha beta fibers only, then both A alpha beta and A delta fibers, and both A and C fibers, as judged by afferent volleys monitored from the sural nerve proximal to the stimulating site. In addition to early components reported previously, a very late component was identified at a latency of 400 to 600 msec following stimulation of the sural nerve with intensities above threshold for A delta fibers. A further increase in stimulation intensity to include activation of C fibers did not reveal any more components. This late component was depressed by a systemic intravenous injection of morphine (2 mg/kg), and intravenous naloxone (0.1 mg/kg) reversed the effect of morphine. The late component of the evoked potential could also be recorded from subcortical tissue after decortication of the sensorimotor cortex. From these results, it appears that a very late component of the cortical evoked potential can be recorded from cats anesthetized with alpha-chloralose. The late component is evoked by activation of peripheral A delta fibers. Furthermore, its morphine sensitivity suggests that this component may be elicited by nociceptive afferent fibers. If further investigations prove this, the late component, which is analogous to human long-latency potentials, could be used in an experimental model for pain research.

摘要

在用α-氯醛糖麻醉的猫身上,研究了体感传入输入所诱发的皮质诱发电位的一个晚期成分。在用不同强度刺激腓肠神经时,从体感运动皮质记录皮质诱发电位。根据在刺激部位近端的腓肠神经监测到的传入冲动,将刺激强度调整为仅激活Aαβ纤维,然后同时激活Aαβ和Aδ纤维,以及A和C纤维。除了先前报道的早期成分外,在用高于Aδ纤维阈值的强度刺激腓肠神经后,在400至600毫秒的潜伏期发现了一个非常晚期的成分。进一步增加刺激强度以包括C纤维的激活,并未发现更多成分。全身静脉注射吗啡(2毫克/千克)可抑制这个晚期成分,静脉注射纳洛酮(0.1毫克/千克)可逆转吗啡的作用。在感觉运动皮质去皮质后,也可从皮质下组织记录到诱发电位的晚期成分。从这些结果来看,似乎在用α-氯醛糖麻醉的猫身上可以记录到皮质诱发电位的一个非常晚期的成分。这个晚期成分是由外周Aδ纤维的激活所诱发的。此外,其对吗啡的敏感性表明这个成分可能是由伤害性传入纤维诱发的。如果进一步的研究证实了这一点,那么这个类似于人类长潜伏期电位的晚期成分可用于疼痛研究的实验模型。

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[Evoked potentials and pain. II. Comparative study of subjective sensations, late components of the cortical potentials and afferent volleys].
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