首页> 外文期刊>Stress: the international journal on the biology of stress >Regulatory interactions of stress and reward on rat forebrain opioidergic and GABAergic circuitry.
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Regulatory interactions of stress and reward on rat forebrain opioidergic and GABAergic circuitry.

机译:应激和奖励对大鼠前脑阿片肌和GABA能回路的调节相互作用。

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Palatable food intake reduces stress responses, suggesting that individuals may consume such ?comfort? food as self-medication for stress relief. The mechanism by which palatable foods provide stress relief is not known, but likely lies at the intersection of forebrain reward and stress regulatory circuits. Forebrain opioidergic and gamma-aminobutyric acid ergic signaling is critical for both reward and stress regulation, suggesting that these systems are prime candidates for mediating stress relief by palatable foods. Thus, the present study (1) determines how palatable ?comfort? food alters stress-induced changes in the mRNA expression of inhibitory neurotransmitters in reward and stress neurocircuitry and (2) identifies candidate brain regions that may underlie comfort food-mediated stress reduction. We used a model of palatable ?snacking? in combination with a model of chronic variable stress followed by in situ hybridization to determine forebrain levels of pro-opioid and glutamic acid decarboxylase (GAD) mRNA. The data identify regions within the extended amygdala, striatum, and hypothalamus as potential regions for mediating hypothalamic-pituitary-adrenal axis buffering following palatable snacking. Specifically, palatable snacking alone decreased pro-enkephalin-A (ENK) mRNA expression in the anterior bed nucleus of the stria terminalis (BST) and the nucleus accumbens, and decreased GAD65 mRNA in the posterior BST. Chronic stress alone increased ENK mRNA in the hypothalamus, nucleus accumbens, amygdala, and hippocampus; increased dynorphin mRNA in the nucleus accumbens; increased GAD65 mRNA in the anterior hypothalamus and BST; and decreased GAD65 mRNA in the dorsal hypothalamus. Importantly, palatable food intake prevented stress-induced gene expression changes in subregions of the hypothalamus, BST, and nucleus accumbens. Overall, these data suggest that complex interactions exist between brain reward and stress pathways and that palatable snacking can mitigate many of the neurochemical alterations induced by chronic stress.
机译:适量的食物摄入可减轻压力反应,表明个人可能会食用这种“舒适感”。食物作为缓解压力的自我药物。可口食品提供缓解压力的机制尚不清楚,但可能位于前脑奖赏和压力调节回路的交叉点。前脑阿霉素和γ-氨基丁酸的能量信号对于奖励和压力调节均至关重要,表明这些系统是通过可口食品调解压力的主要候选者。因此,本研究(1)确定了如何适口的“舒适感”?食物会改变应激诱导的奖赏和应激神经回路中抑制性神经递质的mRNA表达变化,并且(2)确定可能是安慰性食物介导的应激减轻基础的候选大脑区域。我们使用了可口的“零食”模型。结合慢性可变压力模型,然后原位杂交确定前阿片类药物和谷氨酸脱羧酶(GAD)mRNA的水平。数据确定杏仁核,纹状体和下丘脑扩展区域为可口小吃后介导下丘脑-垂体-肾上腺轴缓冲的潜在区域。具体来说,可口的零食单独降低了纹状体末梢(BST)和伏隔核前床核中的前脑啡肽-A(ENK)mRNA表达,并降低了后部BST中的GAD65 mRNA。单独的慢性应激会增加下丘脑,伏隔核,杏仁核和海马中的ENK mRNA。伏隔核中强啡肽mRNA增加;下丘脑前部和BST中GAD65 mRNA增加;并降低了下丘脑GAD65 mRNA的表达。重要的是,可口的食物摄入可防止下丘脑,BST和伏隔核子区域的应激诱导基因表达变化。总体而言,这些数据表明,大脑奖励与应激途径之间存在复杂的相互作用,美味的零食可以缓解慢性应激引起的许多神经化学改变。

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