首页> 外文期刊>Neuropsychopharmacology >|[mu]|-Opioid Receptors are not Involved in Acute Cocaine-Induced Locomotor Activity nor in Development of Cocaine-Induced Behavioral Sensitization in Mice
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|[mu]|-Opioid Receptors are not Involved in Acute Cocaine-Induced Locomotor Activity nor in Development of Cocaine-Induced Behavioral Sensitization in Mice

机译:|μ|-阿片类药物受体不参与可卡因诱导的自发活动,也不参与可卡因诱导的行为敏化

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Although -opioid receptors have been extensively investigated for their role in drug reinforcement, little is known about the contribution of these receptors to the acute and sensitized locomotor response to cocaine. In this study -opioid receptor involvement in acute cocaine-induced locomotor activity and in the development of cocaine-induced behavioral sensitization was evaluated using -opioid receptor knockout mice and chronic naltrexone (NTX) pretreatment as models. In addition, co-administration of the specific -opioid receptor antagonist CTOP with repeated saline or cocaine injections was used to establish the involvement of -opioid receptors in sensitization to the locomotor stimulant effects of cocaine. The acute locomotor response to cocaine (3, 10, 20, or 30 mg/kg i.p.) of -opioid receptor knockout or chronic NTX pretreated mice was not different from the cocaine response of their respective controls. With respect to cocaine-induced behavioral sensitization, induced by daily injections of 20 mg/kg cocaine for 11 subsequent days, -opioid receptor knockout mice developed behavioral sensitization to the locomotor stimulant effects of cocaine (challenge 10 mg/kg i.p.) comparable to wild-type littermates and the -opioid receptor antagonist CTOP did not affect cocaine-induced sensitization either. However, mice that were pretreated with NTX exhibited augmented cocaine-induced behavioral sensitization relative to placebo pretreated controls, which may be ascribed to increased -opioid receptor levels as has been described for chronic NTX pretreated mice. The present findings suggest that -opioid receptors are not required for the acute locomotor response to cocaine nor are they essential for the development of cocaine-induced behavioral sensitization.
机译:尽管已经对阿片类药物受体在药物增强中的作用进行了广泛研究,但对这些受体对可卡因的急性和致敏运动反应的贡献知之甚少。在这项研究中,使用阿片受体敲除小鼠和慢性纳曲酮(NTX)预处理作为模型,评估了阿片受体参与可卡因诱导的自发活动和可卡因诱导的行为敏化的程度。另外,特异性阿片受体拮抗剂CTOP与反复注射盐水或可卡因的共同给药被用于建立阿片受体参与对可卡因的运动刺激作用的致敏作用。对可卡因(3、10、20或30 mg / kg i.p.)的类阿片受体敲除或慢性NTX预处理小鼠的急性运动反应与它们各自对照的可卡因反应没有不同。关于可卡因诱导的行为致敏作用(通过连续11天每天注射20 mg / kg可卡因引起),-阿片类受体敲除小鼠对可卡因的运动刺激作用(挑战性10 mg / kg ip)产生了与野生动物相当的行为致敏作用。型同窝仔和类阿片受体拮抗剂CTOP也不影响可卡因诱导的致敏作用。然而,相对于安慰剂预处理的对照,用NTX预处理的小鼠表现出可卡因诱导的行为敏化增强,这可能归因于阿片类药物受体水平的增加,如针对慢性NTX预处理的小鼠所述。目前的发现表明,对可卡因的急性运动反应不需要阿片受体,对于可卡因诱导的行为敏化的发展,阿片受体也不是必需的。

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