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首页> 外文期刊>Brain, Behavior, and Immunity >Thalamic mast cell activity is associated with sign-tracking behavior in rats
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Thalamic mast cell activity is associated with sign-tracking behavior in rats

机译:丘脑桅杆细胞活性与大鼠的签字跟踪行为有关

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Highlights ? Sign-tracking rats have more thalamic mast cells than goal-tracking rats. ? Sign-tracking rats have more degranulated mast cells than goal-tracking rats. ? Central blockade of mast cell activity with cromolyn blocks sign-tracking. Abstract Mast cells are resident immune cells in the thalamus that can degranulate and release hundreds of signaling molecules (i.e., monoamines, growth factors, and cytokines) both basally and in response to environmental stimuli. Interestingly, mast cell numbers in the brain show immense individual variation in both rodents and humans. We used a Pavlovian conditioned approach (PCA) procedure to examine whether mast cells are associated with individual variation in the attribution of incentive-motivational value to reward-related cues. During the PCA procedure, a lever response-independently predicts the delivery of a food pellet into a magazine, and over training sessions three conditioned responses (CRs) develop: sign-tracking (lever-directed CRs), goal-tracking (magazine-directed CRs), and an intermediate response (both CRs). In Experiment 1, we measured thalamic mast cell number/activation using toluidine blue and demonstrated that sign-trackers have increased degranulated (activated) but not granulated (inactive) mast cells. In Experiment 2, we infused the mast cell inhibitor, cromolyn (200 μg/rat; i.c.v.), immediately before five daily PCA training sessions and demonstrated that mast cell inhibition selectively impairs the acquisition of sign-tracking behavior. Taken together, these results demonstrate that thalamic mast cells contribute to the attribution of incentive-motivational value to reward-related cues and suggest that mast cell inhibition may be a novel target for addiction treatment.
机译:强调 ?签署跟踪大鼠比目标跟踪大鼠更多的丘陵桅杆细胞。还签署跟踪大鼠比目标跟踪大鼠具有更多较劣质的桅杆细胞。还Cromolyn块标志跟踪的桅杆细胞活动中央封锁。摘要肥大细胞是丘脑中的驻留免疫细胞,其在血管腺中可以在基本上和响应于环境刺激的情况下脱节和释放数百个信号分子(即单胺,生长因子和细胞因子)。有趣的是,大脑中的肥大细胞数表现出啮齿动物和人类的巨大个体变异。我们使用了Pavlovian条件方法(PCA)程序来检查桅杆细胞是否与各个变异相关的激励 - 激励价值与奖励相关的线索。在PCA程序期间,杠杆响应 - 独立地预测食品颗粒的输送到杂志上,并在培训会话上进行三个条件响应(CRS)开发:签署跟踪(Lever-Poribed CRS),目标跟踪(杂志 - 导向CRS)和中间响应(两个CR)。在实验1中,我们使用甲苯氨基蓝色测量丘脑桅杆细胞数/活化,并证明符号跟踪器具有增加的溶液(活化)但不造粒(无效)肥大细胞。在实验2中,我们将肥大细胞抑制剂(200μg/大鼠; I.C.V.)注入,在每日五次PCA培训课程之前,并表明桅杆细胞抑制选择性地损害了签名跟踪行为的获取。总之,这些结果表明,丘脑桅杆细胞有助于归因于奖励相关的提示,并表明肥大细胞抑制可以是成瘾治疗的新靶标。

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