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[乙酰胆碱在疼痛的皮质下行调制中的作用]

[Involvement of acetylcholine in corticofugal modulation of pain].

作者信息

Xu W, Yan Y, Shi H, Chen Z

机构信息

Institute of Acupuncture and Moxibustion, China Academy of TCM, Beiaing.

出版信息

Zhen Ci Yan Jiu. 1992;17(2):99-103.

PMID:1288933
Abstract

We have found that after intraperitoneal injecting atropine the analgesic effect of both stimulating Sm I cortex and acupuncture were decreased. It suggests that acetylcholine (ACh) may be involved in the corticofugal modulation of pain. In order to elucidate this idea the effects of stimulating Sm I cortex on tail flick latency (TFL) after ventrical microinjecting atropine were investigated. The experiments were carried out on Wistar rats. Under the state of anaesthesia a pair of silver ball electrodes were put on the dura for electrical stimulating Sm I and the ipsilateral ventricle was cannulated for microinjecting atropine. Recordings were made 5-6 hours or 24 hours after operation. Immediately after cessation of stimulating SmI and 1', 2', 3.5', 5', 7.5', 10' and 15' later TFL were measured consecutively. The results were as follows: 1. The mean value of TFL was 2.44 +/- 0.11 sec (n = 20). It was prolonged (p < 0.05) within 0'-5' after stimulation of SmI. Therefore, it indicated that analgesic effects were produced by stimulating SmI cortex. 2. It was found that under the background of microinjecting atropine (10 micrograms/2 microliters) TFL remained unchanged after stimulating SmI cortex (n = 10, P > 0.05). There was a significant difference between the two treatments: simple stimulating SmI and atropine plus stimulating SmI at the same animals in TFL (P < 0.05) within 0' and 1' after cessation of stimulating SmI. It indicated that the analgesic effects of stimulating SmI cortex were decreased by blocking M-receptors. 3. Under the background of microinjecting normal saline.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们发现,腹腔注射阿托品后,刺激体感皮层I区和针刺的镇痛效果均降低。这表明乙酰胆碱(ACh)可能参与了痛觉的皮质传出调制。为了阐明这一观点,我们研究了脑室微量注射阿托品后刺激体感皮层I区对甩尾潜伏期(TFL)的影响。实验在Wistar大鼠上进行。在麻醉状态下,将一对银球电极置于硬脑膜上以电刺激体感皮层I区,并将同侧脑室插管用于微量注射阿托品。在术后5 - 6小时或24小时进行记录。在停止刺激体感皮层I区后立即以及随后的1'、2'、3.5'、5'、7.5'、10'和15'连续测量甩尾潜伏期。结果如下:1. 甩尾潜伏期的平均值为2.44±0.11秒(n = 20)。刺激体感皮层I区后0' - 5'内其延长(p < 0.05)。因此,表明刺激体感皮层I区可产生镇痛作用。2. 发现在微量注射阿托品(10微克/2微升)的背景下,刺激体感皮层I区后甩尾潜伏期保持不变(n = 10,P > 0.05)。在同一动物中,单纯刺激体感皮层I区与阿托品加刺激体感皮层I区这两种处理在停止刺激体感皮层I区后的0'和1'时甩尾潜伏期存在显著差异(P < 0.05)。这表明阻断M受体可降低刺激体感皮层I区的镇痛效果。3. 在微量注射生理盐水的背景下。(摘要截断于250字)

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