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首页> 外文期刊>PLoS One >Prolonged Restraint Stress Increases IL-6, Reduces IL-10, and Causes Persistent Depressive-Like Behavior That Is Reversed by Recombinant IL-10
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Prolonged Restraint Stress Increases IL-6, Reduces IL-10, and Causes Persistent Depressive-Like Behavior That Is Reversed by Recombinant IL-10

机译:长时间的约束压力会增加IL-6,降低IL-10,并导致持续的抑郁样行为,这种行为会被重组IL-10逆转

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Altered inflammatory cytokine profiles are often observed in individuals suffering from major depression. Recent clinical work reports on elevated IL-6 and decreased IL-10 in depression. Elevated IL-6 has served as a consistent biomarker of depression and IL-10 is proposed to influence depressive behavior through its ability to counterbalance pro-inflammatory cytokine expression. Clinical and animal studies suggest a role for IL-10 in modifying depressive behavior. Murine restraint stress (RST) is regularly employed in the study of behavioral and biological symptoms associated with depressive disorders. While responses to acute RST exposure have been widely characterized, few studies have examined the ongoing and longitudinal effects of extended RST and fewer still have examined the lasting impact during the post-stress period. Consistent with clinical data, we report that a protocol of prolonged murine RST produced altered cytokine profiles similar to those observed in major depressive disorder. Parallel to these changes in circulating cytokines, IL-10 mRNA expression was diminished in the cortex and hippocampus throughout the stress period and following cessation of RST. Moreover, chronic RST promoted depressive-like behavior throughout the 28-day stress period and these depressive-like complications were maintained weeks after cessation of RST. Because of the correlation between IL-10 suppression and depressive behavior and because many successful antidepressant therapies yield increases in IL-10, we examined the effects of IL-10 treatment on RST-induced behavioral changes. Behavioral deficits induced by RST were reversed by exogenous administration of recombinant IL-10. This work provides one of the first reports describing the biological and behavioral impact following prolonged RST and, taken together, this study provides details on the correlation between responses to chronic RST and those seen in depressive disorders.
机译:通常在患有严重抑郁症的个体中观察到炎性细胞因子谱的改变。最近的临床工作报道了抑郁症中IL-6升高和IL-10降低。升高的IL-6一直是抑郁症的一致生物标志物,有人提出IL-10通过其平衡促炎性细胞因子表达的能力来影响抑郁行为。临床和动物研究表明IL-10在改变抑郁行为中的作用。在与抑郁症相关的行为和生物学症状的研究中,经常使用鼠约束应激(RST)。尽管对急性RST暴露的反应已得到广泛表征,但很少有研究检查过延长RST的持续影响和纵向影响,而很少有人研究过应激后期间的持久影响。与临床数据一致,我们报告延长鼠RST的协议产生的细胞因子谱改变与主要抑郁症中观察到的相似。与循环细胞因子的这些变化平行,在整个应激期和RST停止后,皮质和海马中IL-10 mRNA的表达均降低。此外,慢性RST在整个28天的压力期间都促进了抑郁样行为,并且这些抑郁样并发症在RST停止后数周得以维持。由于IL-10抑制与抑郁行为之间的相关性,并且由于许多成功的抗抑郁药在IL-10中的产生量增加,因此我们研究了IL-10治疗对RST诱导的行为变化的影响。通过外源给予重组IL-10可以逆转RST诱导的行为缺陷。这项工作提供了描述长期RST后生物学和行为影响的第一份报告之一,并且合在一起,本研究提供了对慢性RST反应与抑郁症所见反应之间相关性的详细信息。

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