首页> 外文期刊>Behavioural Brain Research: An International Journal >Role of N-methyl-D-aspartate receptors in the long-term effects of repeated social defeat stress on the rewarding and psychomotor properties of cocaine in mice
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Role of N-methyl-D-aspartate receptors in the long-term effects of repeated social defeat stress on the rewarding and psychomotor properties of cocaine in mice

机译:N-甲基-D-天冬氨酸受体在重复社会失败对小鼠可卡因奖励和精神运动特性的长期影响中的作用

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Exposure to social stress increases the vulnerability of experimental animals to the rewarding effects of cocaine and it has been suggested that the glutamatergic system could be involved in these effects of stress. The aim of this work is to determine the role of N-methyl-D-aspartate (NMDA) glutamate receptors in the influence of social stress on the conditioned place preference and locomotor sensitization induced by cocaine. Mice treated with saline or NMDA antagonist memantine (5 or 10 mg/kg) underwent repeated social defeat or were kept in the exploration control condition. After three weeks, all groups (SAL + RSD, M5 + RSD, M10 + RSD, SAL + EXP, M5 + EXP and M10 + EXP) were conditioned with 1 mg/kg of cocaine (experiment 1). After nine weeks, each group was subdivided into two groups: one received saline and the other cocaine (25 mg/kg) on 3 consecutive days. After a 5-day interval, all the animals received a challenge of cocaine (10 mg/kg) and their locomotor activity was registered (experiment 2). Only stressed animals developed place preference, an effect prevented by the low dose of memantine. Control defeated mice (but not those treated with memantine) showed greater activity than mice not exposed to stress. Our results show that glutamate NMDA receptors are involved in the higher vulnerability to cocaine effects provoked by exposure to social defeat. They also suggest that memantine could be a useful therapeutic tool for treatment of cocaine dependent individuals exposed to stress conditions.
机译:暴露于社会压力会使实验动物对可卡因的奖励作用的脆弱性,并且已经提出了谷氨酸体系可以参与这些压力的影响。这项工作的目的是确定N-甲基-D-天冬氨酸(NMDA)谷氨酸受体在社会压力对可卡因诱导的条件偏好和运动致敏的影响下的作用。用盐水或NMDA拮抗剂Memantine(5或10mg / kg)处理的小鼠进行了重复的社会失败,或者在勘探控制条件下保持。三周后,所有组(SAL + RSD,M5 + RSD,M10 + RSD,SAL + EXP,M5 + EXP和M10 + EXP)都有1毫克/千克可卡因(实验1)。九周后,将每组细分为两组:连续3天接受盐水和其他可卡因(25mg / kg)。经过5天的间隔后,所有动物都接受了可卡因(10mg / kg)的挑战,并登记了其运动活性(实验2)。只有强调的动物开发了偏好的偏好,效果低剂量的致致症。控制击败的小鼠(但不是用Memantine处理的小鼠显示出比未暴露于应力的小鼠更大的活性。我们的研究结果表明,谷氨酸NMDA受体参与通过暴露于社会失败引发的可卡因效应的高脆弱性。他们还表明,Memantine可以是一种有用的治疗工具,用于治疗暴露于压力条件的可卡因依赖性个体。

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