Jiacai Yang, Lin Zhang, Jian-Ping Dai, Jun Zeng, Xiao-Xuan Chen, Ze-Feng Xie, Kang-Sheng Li, Yun Su
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Thereafter, mice in the acute stress group received a single 60-min cat exposure, and mice in the chronic group received daily 60-min cat exposure for 14 consecutive days. The plasma CS and TNF-α were determined by ELISA, the hypothalamic CRH mRNA and hippocampal GR mRNA were detected by real-time PCR, and the hippocampal GR protein was detected by western blot analysis.</p><p><strong>Results: </strong>The results revealed that the levels of plasma CS were significantly elevated after chronic predatory exposure in both right-pawed and left-pawed mice; the right-pawed mice exhibited a higher plasma CS level than the left-pawed mice. Similarly, the acute or chronic cat exposure could induce the release of plasma TNF-α, and the left-pawed mice tended to show a higher level after the acute stress. Chronic stress significantly upregulated the expression of hypothalamic CRH mRNA in both left-pawed and right-pawed mice. Normally, the left-pawed mice exhibited a higher GR expression in the hippocampus than the right-pawed mice. After the cat exposure, the expression of GR in both left-pawed and right-pawed mice was revealed to be greatly downregulated.</p><p><strong>Conclusion: </strong>Our findings indicate that predatory stress can invoke a differential response of stressful elements in behavior-lateralized mice. 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引用次数: 0
摘要
背景:掠食性应激作为一种心理应激源可引起下丘脑-垂体-肾上腺(HPA)轴的激活,该轴参与神经免疫内分泌网络的对话。大脑已被证明通过侧化的方式调节下丘脑轴的活动。在本研究中,我们研究了行为侧化小鼠HPA回路的关键元件,包括CRH、GR和多功能细胞因子,以确定它们在捕食者暴露时的变化。方法:将行为偏侧小鼠分为左爪小鼠和右爪小鼠。此后,急性应激组小鼠接受单次60分钟猫暴露,慢性应激组小鼠连续14天每天接受60分钟猫暴露。ELISA法检测血浆CS和TNF-α, real-time PCR法检测下丘脑CRH mRNA和海马GR mRNA, western blot法检测海马GR蛋白。结果:右脚和左脚小鼠慢性掠食性暴露后血浆CS水平均显著升高;右撇子小鼠的血浆CS水平高于左撇子小鼠。同样,急性或慢性猫暴露均可诱导血浆TNF-α的释放,且左爪小鼠在急性应激后往往表现出更高的水平。慢性应激显著上调左、右脚小鼠下丘脑CRH mRNA的表达。正常情况下,左爪小鼠海马GR表达高于右爪小鼠。猫暴露后,左、右爪小鼠中GR的表达均明显下调。结论:我们的研究结果表明,掠夺性应激可以引起行为侧化小鼠应激因素的差异反应。其中一些由行为侧化形成的反应可能有助于促进对各种刺激的适应。
Differential responses of stressful elements to predatory exposure in behavior-lateralized mice.
Background: Predatory stress as a psychological stressor can elicit the activation of the hypothalamic-pituitary-adrenal (HPA) axis, which is involved in the dialogue of the neuroimmunoendocrine network. The brain has been proven to regulate the activity of the HPA axis by way of lateralization. In the present study, we probed the pivotal elements of the HPA circuitry including CRH, GR and a multifunctional cytokine in behavior-lateralized mice to determine their changes when the animals were subjected to predator exposure.
Methods: Behavior-lateralized mice were classified into left-pawed and right-pawed mice through a paw-preference test. Thereafter, mice in the acute stress group received a single 60-min cat exposure, and mice in the chronic group received daily 60-min cat exposure for 14 consecutive days. The plasma CS and TNF-α were determined by ELISA, the hypothalamic CRH mRNA and hippocampal GR mRNA were detected by real-time PCR, and the hippocampal GR protein was detected by western blot analysis.
Results: The results revealed that the levels of plasma CS were significantly elevated after chronic predatory exposure in both right-pawed and left-pawed mice; the right-pawed mice exhibited a higher plasma CS level than the left-pawed mice. Similarly, the acute or chronic cat exposure could induce the release of plasma TNF-α, and the left-pawed mice tended to show a higher level after the acute stress. Chronic stress significantly upregulated the expression of hypothalamic CRH mRNA in both left-pawed and right-pawed mice. Normally, the left-pawed mice exhibited a higher GR expression in the hippocampus than the right-pawed mice. After the cat exposure, the expression of GR in both left-pawed and right-pawed mice was revealed to be greatly downregulated.
Conclusion: Our findings indicate that predatory stress can invoke a differential response of stressful elements in behavior-lateralized mice. Some of these responses shaped by behavioral lateralization might be helpful for facilitating adaption to various stimuli.
期刊介绍:
A well-established journal in the field of behavioral and cognitive neuroscience, Behavioral and Brain Functions welcomes manuscripts which provide insight into the neurobiological mechanisms underlying behavior and brain function, or dysfunction. The journal gives priority to manuscripts that combine both neurobiology and behavior in a non-clinical manner.