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神经降压素、β-内啡肽和蛙皮素对小鼠乙醇诱导行为的影响。

The effects of neurotensin, beta-endorphin, and bombesin on ethanol-induced behaviors in mice.

作者信息

Luttinger D, Frye G D, Nemeroff C B, Prange A J

出版信息

Psychopharmacology (Berl). 1983;79(4):357-63. doi: 10.1007/BF00433418.

DOI:10.1007/BF00433418
PMID:6304802
Abstract

The effects of the three peptides neurotensin, beta-endorphin, and bombesin on ethanol-induced behaviors were studied in mice. Intracisternal administration of these peptides to mice prolonged the duration of sleep induced by ethanol (5.2 g/kg). Neurotensin and beta-endorphin also enhanced ethanol-induced hypothermia. None of the peptides, when administered alone, produced sleep. However, all three compounds impaired the aerial righting reflex and induced sleep when followed by an IP dose of ethanol (3.5 g/kg), which alone did not induce sleep. These results, taken together with previous findings, suggest that neuropeptides may be involved in the complex mechanisms of action of ethanol on the CNS.

摘要

研究了三种肽——神经降压素、β-内啡肽和蛙皮素对小鼠乙醇诱导行为的影响。向小鼠脑池内注射这些肽可延长乙醇(5.2克/千克)诱导的睡眠时间。神经降压素和β-内啡肽还增强了乙醇诱导的体温过低。单独注射这些肽均不会产生睡眠。然而,当腹腔注射乙醇(3.5克/千克,单独使用该剂量不会诱导睡眠)后,这三种化合物均会损害空中翻正反射并诱导睡眠。这些结果与之前的研究结果共同表明,神经肽可能参与了乙醇对中枢神经系统作用的复杂机制。

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1
The effects of neurotensin, beta-endorphin, and bombesin on ethanol-induced behaviors in mice.神经降压素、β-内啡肽和蛙皮素对小鼠乙醇诱导行为的影响。
Psychopharmacology (Berl). 1983;79(4):357-63. doi: 10.1007/BF00433418.
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本文引用的文献

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Antagonism of ethanol induced sleep-time by alpha-msh, MSH/ACTH4-10 and naloxone.α-促黑素、促黑素/促肾上腺皮质激素4-10和纳洛酮对乙醇诱导睡眠时间的拮抗作用。
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Acute and chronic ethanol treatment changes endorphin levels in brain and pituitary.
Psychopharmacology (Berl). 1980;68(3):221-7. doi: 10.1007/BF00428107.
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Modification of the actions of ethanol by centrally active peptides.中枢活性肽对乙醇作用的调节
Peptides. 1981;2 Suppl 1:99-106. doi: 10.1016/0196-9781(81)90063-2.
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Enhancement of ethanol-induced sedation and hypothermia by centrally administered neurotensin, beta-endorphin and bombesin.
Neuropharmacology. 1981 Mar;20(3):305-9. doi: 10.1016/0028-3908(81)90139-8.
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