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Synergistic effect of cholecystokinin octapeptide and angiotensin II in reversal of morphine induced analgesia in rats.

作者信息

Han Nian-Lin, Luo Fei, Bian Zhu-Ping, Han Ji-Sheng

机构信息

Neuroscience Research Institute, Beijing Medical University, Beijing 100083, PR China Department of Physiology, Yian-Bei Nursing School, Datong, Shanxi, PR China.

出版信息

Pain. 2000 Apr;85(3):465-469. doi: 10.1016/S0304-3959(99)00294-8.

DOI:10.1016/S0304-3959(99)00294-8
PMID:10781920
Abstract

The aim of this paper is to study the synergistic anti-analgesic effect of angiotensin II (Ang II) plus cholecystokinin octapeptide (CCK-8). Our previous studies have shown that both CCK-8 and Ang II are potent anti-opioid substances. Intracerebroventricular (i.c.v.) injection of CCK-8 or Ang II dose-dependently antagonizes morphine-induced analgesia (MIA). In the present study, we observed the combined effect of CCK-8 and Ang II in antagonizing MIA. CCK-8 and Ang II were injected intracerebroventricularly to rats in various proportions and doses. The results were analyzed with isobolographic analysis. Combined injection of CCK-8 and Ang II in a ratio of 1 ng: 2.5 microg or 1 ng: 5 microg produced significantly greater effect in antagonizing MIA. The ED(50) of the two ratios are only 18.5% and 27.5%, respectively, of the theoretical dose of simple addition. We conclude that CCK-8 and Ang II used in such dose ratios may antagonize MIA synergistically.

摘要

相似文献

1
Synergistic effect of cholecystokinin octapeptide and angiotensin II in reversal of morphine induced analgesia in rats.
Pain. 2000 Apr;85(3):465-469. doi: 10.1016/S0304-3959(99)00294-8.
2
Cholecystokinin octapeptide (CCK-8) antagonizes morphine analgesia in nucleus accumbens of the rat via the CCK-B receptor.
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3
[Antagonism of morphine analgesia and electroacupuncture analgesia by cholecystokinin octapeptide (CCK-8) administered in periaqueductal gray (PAG) of the rabbits].
Sheng Li Xue Bao. 1989 Aug;41(4):388-94.
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Is cholecystokinin octapeptide (CCK-8) a candidate for endogenous anti-opioid substrates?胆囊收缩素八肽(CCK-8)是内源性抗阿片样物质底物的候选物吗?
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Differential effects of sulfated cholecystokinin octapeptide and proglumide injected intrathecally on antinociception induced by beta-endorphin and morphine administered intracerebroventricularly in mice.鞘内注射硫酸化胆囊收缩素八肽和丙谷胺对小鼠脑室内注射β-内啡肽和吗啡诱导的镇痛作用的差异影响。
Eur J Pharmacol. 1990 Apr 25;179(3):329-38. doi: 10.1016/0014-2999(90)90173-4.
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[Cholecystokinin octapeptide (CCK-8) antagonizes morphine analgesia in amygdala of the rat].[胆囊收缩素八肽(CCK-8)拮抗大鼠杏仁核中的吗啡镇痛作用]
Sheng Li Xue Bao. 1993 Oct;45(5):470-8.
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Involvement of different subtypes of cholecystokinin receptors in opioid antinociception in the mouse.不同亚型的胆囊收缩素受体在小鼠阿片类镇痛中的作用
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Cholecystokinin administered intrathecally selectively antagonizes intracerebroventricular beta-endorphin-induced tail-flick inhibition in the mouse.鞘内注射胆囊收缩素可选择性拮抗小鼠脑室内β-内啡肽诱导的甩尾抑制。
J Pharmacol Exp Ther. 1992 Mar;260(3):1086-92.
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Reversal of tolerance to morphine but no potentiation of morphine-induced analgesia by antiserum against cholecystokinin octapeptide.
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10
Intracerebroventricular administration of angiotensin II attenuates morphine-induced analgesia in mice.
Neuropharmacology. 1985 Nov;24(11):1131-4. doi: 10.1016/0028-3908(85)90204-7.

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