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有害皮肤刺激对大鼠甩尾反射的易化作用:P物质类似物的拮抗作用。

Facilitation of the tail-flick reflex by noxious cutaneous stimulation in the rat: antagonism by a substance P analogue.

作者信息

Cridland R A, Henry J L

机构信息

Department of Psychiatry, McGill University, Montreal, Que. Canada.

出版信息

Brain Res. 1988 Oct 11;462(1):15-21. doi: 10.1016/0006-8993(88)90579-3.

Abstract

Effects of noxious cutaneous stimulation on the tail flick reflex were examined in the anaesthetized rat. Noxious stimulation was applied by immersing the distal 4 cm of the tail in water at 55 degrees C for 1.5 min. The tail flick reflex was tested at 3 min intervals by applying a noxious radiant heat stimulus to a region of the tail 10 cm proximal to the tip. Tail immersion reduced reaction time to tail flick by 30% and 20% at 0.5 and 3.5 min after immersion, respectively. Reaction time returned to control at 6.5 min and tended to increase above baseline values at 9.5 and 12.5 min. Naloxone (10 mg/kg, i.p.) potentiated the effects of tail immersion on reaction time and prevented the increase above baseline. When the surface temperature of the skin used to evoke the tail flick reflex was raised by 10 degrees C using innocuous radiant heat, reaction time was not significantly different from the control, suggesting that an increase in skin temperature per se is insufficient to account for the response to immersion. Intrathecal administration of a substance P antagonist (1 nmol) attenuated the response to tail immersion. These results indicate that noxious cutaneous stimulation may release an agent in the spinal cord which facilitates the tail flick reflex, and that this agent is antagonized by a substance P antagonist.

摘要

在麻醉大鼠中研究了有害皮肤刺激对甩尾反射的影响。通过将尾巴远端4厘米浸入55摄氏度的水中1.5分钟来施加有害刺激。每隔3分钟,通过对尾巴尖端近端10厘米处的区域施加有害的辐射热刺激来测试甩尾反射。尾巴浸入后0.5分钟和3.5分钟时,甩尾的反应时间分别缩短了30%和20%。反应时间在6.5分钟时恢复到对照水平,并在9.5分钟和12.5分钟时趋于高于基线值。纳洛酮(10毫克/千克,腹腔注射)增强了尾巴浸入对反应时间的影响,并防止了反应时间高于基线值的增加。当使用无害的辐射热将用于诱发甩尾反射的皮肤表面温度升高10摄氏度时,反应时间与对照无显著差异,这表明皮肤温度本身的升高不足以解释对浸入的反应。鞘内注射P物质拮抗剂(1纳摩尔)减弱了对尾巴浸入的反应。这些结果表明,有害的皮肤刺激可能在脊髓中释放一种促进甩尾反射的物质,并且这种物质被P物质拮抗剂所拮抗。

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