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导水管周围灰质中的CCK(B)受体参与大鼠冷水甩尾试验中的电针镇痛作用。

CCK(B) receptors in the periaqueductal grey are involved in electroacupuncture antinociception in the rat cold water tail-flick test.

作者信息

Chen X H, Geller E B, Adler M W

机构信息

Department of Pharmacology, Temple University School of Medicine, Philadelphia, PA 19140, USA.

出版信息

Neuropharmacology. 1998 Jun;37(6):751-7. doi: 10.1016/s0028-3908(98)00028-8.

DOI:10.1016/s0028-3908(98)00028-8
PMID:9707289
Abstract

Cholecystokinin octapeptide (CCK-8) (0.25-2.0 ng), the CCK(A) receptor antagonist L-364,718 (60-100 ng) or the CCK(B) receptor antagonist L-365,260 (0.3125-1.25 ng) was administered into the periaqueductal grey (PAG) of male SD rats. The antinociceptive effect induced by electroacupuncture (EA) stimulation of different frequencies was then measured by the cold water tail-flick (CWT) test. The results showed that (1) microinjection of CCK-8 into the PAG can significantly block the antinociceptive effect induced by all frequencies of EA stimulation. The effectiveness of the blockade was 100 > 2 Hz. In addition, CCK-8 blocks the antinociception seen following termination of the electrical stimulation at 100 Hz; (2) microinjection of L-365,260 (1.25 ng) into the PAG significantly increased the 100 Hz EA antinociceptive effect but not the 2 Hz EA antinociceptive effect and microinjection of L-364,718 into PAG did not affect either 2 or 100 Hz EA antinociception. These results demonstrate that CCK-8 in the PAG can antagonize the antinociceptive effect induced by EA stimulation, and the CCK effect is likely to be mediated by the CCK(B) receptor, but not the CCK(A) receptor.

摘要

将八肽胆囊收缩素(CCK - 8)(0.25 - 2.0纳克)、CCK(A)受体拮抗剂L - 364,718(60 - 100纳克)或CCK(B)受体拮抗剂L - 365,260(0.3125 - 1.25纳克)注入雄性SD大鼠的导水管周围灰质(PAG)。然后通过冷水甩尾(CWT)试验测量不同频率电针(EA)刺激诱导的抗伤害感受作用。结果表明:(1)向PAG微量注射CCK - 8可显著阻断所有频率EA刺激诱导的抗伤害感受作用。阻断效果为100 > 2赫兹。此外,CCK - 8可阻断100赫兹电刺激终止后出现的抗伤害感受;(2)向PAG微量注射L - 365,260(1.25纳克)可显著增强100赫兹EA的抗伤害感受作用,但不影响2赫兹EA的抗伤害感受作用,而向PAG微量注射L - 364,718对2赫兹或100赫兹EA的抗伤害感受均无影响。这些结果表明,PAG中的CCK - 8可拮抗EA刺激诱导的抗伤害感受作用,且CCK的作用可能由CCK(B)受体介导,而非CCK(A)受体。

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