首页> 外文期刊>Behavioural Brain Research: An International Journal >An examination of the effects of subthalamic nucleus inhibition or μ-opioid receptor stimulation on food-directed motivation in the non-deprived rat
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An examination of the effects of subthalamic nucleus inhibition or μ-opioid receptor stimulation on food-directed motivation in the non-deprived rat

机译:检验丘脑下核抑制或μ阿片受体刺激对未剥夺大鼠食物定向动机的影响

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The subthalamic nucleus (STN) serves important functions in regulating movement, cognition, and motivation and is connected with cortical and basal ganglia circuits that process reward and reinforcement. In order to further examine the role of the STN on motivation toward food in non-deprived rats, these experiments studied the effects of pharmacological inhibition or μ-opioid receptor stimulation of the STN on the 2-h intake of a sweetened fat diet, the amount of work exerted to earn sucrose on a progressive ratio 2 (PR-2) schedule of reinforcement, and performance on a differential reinforcement of low-rate responding (DRL) schedule for sucrose reward. Separate behavioral groups (N=6-9) were tested following bilateral inhibition of the STN with the GABA A receptor agonist muscimol (at 0-5ng/0.5μl/side) or following μ-opioid receptor stimulation with the agonist D-Ala 2, N-MePhe 4, Gly-ol-enkephalin (DAMGO; at 0, 0.025 or 0.25μg/0.5μl/side). Although STN inhibition increased ambulatory behavior during 2-h feeding sessions, it did not significantly alter intake of the sweetened fat diet. STN inhibition also did not affect the breakpoint for sucrose pellets during a 1-h PR-2 reinforcement schedule or impact the number of reinforcers earned on a 1-h DRL-20s reinforcement schedule in non-deprived rats. In contrast, STN μ-opioid receptor stimulation significantly increased feeding on the palatable diet and reduced the reinforcers earned on a DRL-20 schedule, although DAMGO microinfusions had no effect on PR-2 performance. These data suggest that STN inhibition does not enhance incentive motivation for food in the absence of food restriction and that STN μ-opioid receptors play an important and unique role in motivational processes.
机译:丘脑下核(STN)在调节运动,认知和动机方面起重要作用,并与处理奖励和增强功能的皮质和基底神经节回路相连。为了进一步检查STN在非剥夺大鼠中对食物动机的作用,这些实验研究了STN的药理抑制或μ阿片受体刺激对甜味脂肪饮食2小时摄入的影响。在渐进比率2(PR-2)强化计划中获得蔗糖所进行的工作量,以及在低速响应(DRL)进度表中对蔗糖奖励进行差异强化时的表现。在分别用GABA A受体激动剂麝香酚双侧抑制STN(0-5ng /0.5μl/侧)或用激动剂D-Ala 2刺激μ阿片受体后,测试了单独的行为组(N = 6-9) ,N-MePhe 4,乙二醇-脑啡肽(DAMGO;在0、0.025或0.25μg/0.5μl/面)。尽管STN抑制作用在2小时的喂食期间增加了行走行为,但它并未显着改变甜味脂肪饮食的摄入量。 STN抑制也不会影响1-h PR-2强化时间表中蔗糖颗粒的断点,也不会影响非剥夺大鼠中1-h DRL-20s强化时间表中获得的强化剂数量。相比之下,尽管DAMGO微量输注对PR-2的性能没有影响,但STNμ阿片受体的刺激显着增加了可口饮食的摄食并降低了按DRL-20时间表获得的强化剂。这些数据表明,在没有食物限制的情况下,STN抑制作用不会增强食物的刺激动机,并且STNμ阿片受体在刺激过程中起着重要而独特的作用。

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