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去甘氨酰胺9、(精氨酸8)加压素和加压素抗血清对大鼠静脉注射可卡因自我给药习得的影响。

Effects of desglycinamide9, (Arg8) vasopressin and vasopressin antiserum on the acquisition of intravenous cocaine self-administration in the rat.

作者信息

de Vry J, Donselaar I, van Ree J M

机构信息

Rudolf Magnus Institute for Pharmacology, Medical Faculty, University of Utrecht, The Netherlands.

出版信息

Life Sci. 1988;42(26):2709-15. doi: 10.1016/0024-3205(88)90247-0.

DOI:10.1016/0024-3205(88)90247-0
PMID:3290606
Abstract

The effect of the vasopressin neuropeptide desglycinamide9, (Arg8) vasopressin (DGAVP) on the acquisition of intravenous cocaine self-administration was studied. Rats were tested under conditions of reduced body weight in a continuous reinforcement operant procedure, during five daily 3 h sessions. Under these conditions, the rate of self-administration obtained with 0.125 and 0.25, but not 0.063 mg.ml-1 cocaine, exceeded the rate obtained with saline. Daily pretreatment with DGAVP (5 micrograms/rat, s.c.) decreased self-administration of 0.125 and 0.25 mg.ml-1 cocaine to the level obtained with saline, but had no effect on self-administration of 0.063 mg.ml-1 cocaine and saline. Using a similar procedure, it was shown that daily intracerebroventricular pretreatment with vasopressin antiserum significantly increased self-administration of 0.125 mg.ml-1 cocaine, without affecting self-administration of 0.063 and 0.25 mg.ml-1 cocaine and saline. The results support previous findings obtained with vasopressin neuropeptides in drug self-administration studies and suggest that DGAVP decreases the acquisition of cocaine self-administration by attenuating the reinforcing effects of cocaine and that endogenous vasopressin may be involved in the acquisition of cocaine self-administration.

摘要

研究了血管加压素神经肽去甘氨酰胺9,(精氨酸8)血管加压素(DGAVP)对静脉注射可卡因自我给药习得的影响。在连续强化操作性程序中,在体重减轻的条件下对大鼠进行测试,每天进行5次,每次3小时。在这些条件下,0.125和0.25(而非0.063mg/ml)可卡因的自我给药速率超过了生理盐水的给药速率。每天皮下注射DGAVP(5微克/只大鼠)预处理可使0.125和0.25mg/ml可卡因的自我给药量降至生理盐水的给药水平,但对0.063mg/ml可卡因和生理盐水的自我给药量没有影响。采用类似程序表明,每天脑室注射血管加压素抗血清预处理可显著增加0.125mg/ml可卡因的自我给药量,而不影响0.063和0.25mg/ml可卡因以及生理盐水的自我给药量。这些结果支持了先前在药物自我给药研究中使用血管加压素神经肽获得的发现,并表明DGAVP通过减弱可卡因的强化作用降低了可卡因自我给药的习得,且内源性血管加压素可能参与了可卡因自我给药的习得。

相似文献

1
Effects of desglycinamide9, (Arg8) vasopressin and vasopressin antiserum on the acquisition of intravenous cocaine self-administration in the rat.去甘氨酰胺9、(精氨酸8)加压素和加压素抗血清对大鼠静脉注射可卡因自我给药习得的影响。
Life Sci. 1988;42(26):2709-15. doi: 10.1016/0024-3205(88)90247-0.
2
Vasopressin neuropeptides and acquisition of heroin and cocaine self-administration in rats.血管加压素神经肽与大鼠海洛因和可卡因自我给药行为的习得
Life Sci. 1988;42(10):1091-9. doi: 10.1016/0024-3205(88)90565-6.
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The effect of desglycinamide-(Arg8)-vasopressin (DGAVP) on the acquisition of free-choice alcohol drinking in rhesus monkeys.去甘氨酰胺-(精氨酸8)-加压素(DGAVP)对恒河猴自由选择饮酒习性形成的影响。
Alcohol Clin Exp Res. 1991 Feb;15(1):72-9. doi: 10.1111/j.1530-0277.1991.tb00520.x.
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Vasopressin(1-8) (des-glycinamide9-[Arg8]vasopressin) is an endogenous peptide present in rat plasma.
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Des-Gly-vasopressin improves acquisition and slows extinction of autoshaped behavior.去甘氨加压素可改善自动形成行为的习得并减缓其消退。
Eur J Pharmacol. 1983 Apr 22;89(1-2):43-51. doi: 10.1016/0014-2999(83)90606-4.
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Des-Gly9-[Arg8]-vasopressin may facilitate methadone detoxification of heroin addicts.
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Food deprivation and acquisition of intravenous cocaine self-administration in rats: effect of naltrexone and haloperidol.
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Studies on desglycinamide arginine vasopressin and scopolamine in a modified/lever-touch autoshaping model of learning/memory in rats.在大鼠学习/记忆的改良/杠杆触碰自动成型模型中对去甘氨酰胺精氨酸加压素和东莨菪碱的研究。
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Differential effects of DGAVP on acquisition and extinction of active avoidance behavior.去甘氨酰精氨酸加压素(DGAVP)对主动回避行为的习得和消退的不同影响。
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Analysis of the influence of vasopressin neuropeptides on social recognition of rats.血管加压素神经肽对大鼠社会认知的影响分析
Eur Neuropsychopharmacol. 1991 May;1(2):123-6. doi: 10.1016/0924-977x(91)90713-5.

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Arginine vasopressin gene expression changes within the nucleus accumbens during environment elicited cocaine-conditioned response in rats.在大鼠环境诱发可卡因条件反应过程中,伏隔核内精氨酸加压素基因表达的变化。
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Transport of desglycinamide-arginine vasopressin across the blood-brain barrier in rats as evaluated by the unit impulse response methodology.
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Pharm Res. 1990 Mar;7(3):293-8. doi: 10.1023/a:1015838532048.