热板试验中胆囊收缩素受体在抗痛性诱导中的作用。

M Rezayat, A Rahnavard, M R Zarrindast
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引用次数: 9

摘要

本研究在小鼠热板实验中评价了胆囊收缩素受体激动剂的抗伤害性作用。皮下注射缩胆素八肽(cholecystokinin-8;0.001, 0.005, 0.01, 0.05和0.1 mg/kg),无硫化胆囊收缩素八肽(胆囊收缩素8u;0.1 mg/kg)或小黄精(0.25 mg/kg)产生抗伤感。给药胆囊收缩素四肽(胆囊收缩素-4;0.25、0.5、1.0 mg/kg)对热板试验无影响。皮下注射选择性胆囊收缩素受体拮抗剂MK-329(0.125、0.25和0.5 mg/kg)或L-365,260(0.125、0.25和0.5 mg/kg),没有产生抗伤害性反应。用胆囊收缩素受体拮抗剂或纳洛酮(0.5 mg/kg和1 mg/kg)预处理小鼠,可显著降低胆囊收缩素-8和小黄精诱导的抗伤害反应。结果表明,单次给药胆囊收缩素受体激动剂可能通过胆囊收缩素受体介导产生抗伤害感受作用。根据吗啡和纳洛酮给药的结果,结论是胆囊收缩素和阿片机制之间可能存在相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of cholecystokinin receptors in induction of antinociception in hot-plate test.

In the present study, the antinociceptive effect of cholecystokinin receptor agonists in the hot-plate test in mice has been evaluated. Subcutaneous administration of cholecystokinin octapeptide (cholecystokinin-8; 0.001, 0.005, 0.01, 0.05, and 0.1 mg/kg), unsulfated cholecystokinin octapeptide (cholecystokinin-8U; 0.1 mg/kg) or caerulein (0.25 mg/kg) produced antinociception. Administration of the cholecystokinin tetrapeptide (cholecystokinin-4; 0.25, 0.5 and 1.0 mg/kg) had no effect in the hot-plate test. Subcutaneous injection of the selective cholecystokinin receptor antagonists, MK-329 (0.125, 0.25 and 0.5 mg/kg) or L-365,260 (0.125, 0.25 and 0.5 mg/kg), produced no antinociceptive response. When the animals were pretreated with the cholecystokinin receptor antagonists or naloxone (0.5 and 1 mg/kg), a significant decrease in the antinociceptive response induced by cholecystokinin-8 and caerulein was obtained. The results indicate that single administration of cholecystokinin receptor agonists could produce an antinociceptive effect which is probably mediated via cholecystokinin receptors. With respect to the results obtained from morphine and naloxone administration, it is concluded that there may be an interaction between cholecystokinin and opiate mechanisms.

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