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作 者:赵书芬[1] 辛黎[1] 冯甲棣[1] 李亘松[1] 姜锡然[1] 张小玲 聂志伟[1]
机构地区:[1]中国医科大学生理教研室
出 处:《中国应用生理学杂志》1997年第1期57-59,共3页Chinese Journal of Applied Physiology
基 金:国家自然科学基金
摘 要:本研究旨在了解弓状核内的阿片受体在体温调节中的作用。研究使用细胞介素IL1β做致热源。以自动推进器向SD雄性大鼠弓状核微量注射1μ1IL1β。在给药前30min分别向弓状核微量注射通常阿片受体拮抗剂纳洛酮(Nal)、阿片受体μ、δ和κ各自特异性拮抗剂CTAP、NTI和norBNI做预处理,用生理盐水(Sal)做对照。结果表明:IL1β所致的升体温效应能被Nal和CTAP阻断,提示弓状核中的阿片受体(主要是μ受体)参与或介导了IL1β的致热效应;δ和κ受体特异性拮抗剂阻断IL1β所致的体温升高效应不明显。提示δ和κ阿片受体参与体温调节的可能性较小。对照ARH和POAH中阿片受体在IL1β所致发热中的作用可发现:二者作用极为相似,这一结果有力地支持了弓状核是体温调节中枢重要组成部分的观点。The present study is to define the role played by the opioid receptors of ARH in the regulation of body temperature. lμl of IL 1β (as pyrogen) was injected into the ARH of male Sprague Dawley rat with an automatic micromanipulator to induce hyperthermia.30 minutes prior to the injection of pyrogen,the experimental groups were pre treated with general opioid receptor antagonist naloxone (Nal),selective μ,δ,κ receptor antagonists CTAP,NTI,nor BNI respectively.Controls were pre treated with saline.The results showed that IL 1β induced hyperthermia was blocked by Nal and CTAP,suggesting the involvement of, or mediation by,ARH opioid receptors (mainly the μ type) in IL 1β induced hyperthermia.The blockade by δ and κ antagonists was not remarkable.Thus their participation in this process is less likely.The similarity between the roles of opioid receptors of ARH and POAH in IL 1β induced hyperthermia strongly supports the view that ARH may be an important component of the thermoregulatory center.
分 类 号:R338.27[医药卫生—人体生理学]
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