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可乐定在猴子体内的镇痛作用部位及方式。

The site and the mode of analgesic actions exerted by clonidine in monkeys.

作者信息

Wang Y C, Su C F, Lin M T

出版信息

Exp Neurol. 1985 Dec;90(3):479-88. doi: 10.1016/0014-4886(85)90146-3.

Abstract

We used intracerebral administration of clonidine in monkeys to map effective sites for analgesia. The jaw opening reflex elicited by tooth pulp stimulation was used for analgesia testing. We found that the most consistently effective sites for analgesia in monkeys are in at least three brain regions: the diencephalic periventricular gray, the dorsal raphe nuclei, and the periaqueductal gray. In addition, the analgesia induced by intracerebral administration of clonidine was effectively antagonized by pretreatment of animals with either naloxone (a narcotic antagonist) or yohimbine (an alpha-adrenergic antagonist). These results suggest the existence of an opiate and an adrenergic antinociceptive mechanism in the diencephalic periventricular gray, the dorsal raphe nuclei, and the periaqueductal gray activated by clonidine in primates.

摘要

我们通过向猴子脑内注射可乐定来绘制镇痛有效位点。利用牙髓刺激引发的张口反射进行镇痛测试。我们发现,在猴子中最持续有效的镇痛位点至少分布在三个脑区:间脑脑室周围灰质、中缝背核和导水管周围灰质。此外,用纳洛酮(一种麻醉拮抗剂)或育亨宾(一种α-肾上腺素能拮抗剂)预处理动物可有效拮抗脑内注射可乐定所诱导的镇痛作用。这些结果表明,在灵长类动物中,可乐定激活的间脑脑室周围灰质、中缝背核和导水管周围灰质中存在阿片类和肾上腺素能抗伤害感受机制。

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