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Neural and behavioral responses to systemic immunologic stimuli: a consideration of bacterial T cell superantigens.

机译:对全身免疫刺激的神经和行为反应:细菌T细胞超抗原的考虑。

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摘要

Immune responses represent a source of systemic stress which impacts the brain and modifies various neuroendocrine and behavioral functions. Therefore, the immune system has been conceived of as a potential contributor to stress-related behavioral abnormalities, such as depression. Much of this knowledge has been gained through research focused largely on the administration of cytokines and/or bacterial endotoxin (eg., LPS), which targets innate immune cells, such as macrophages. However, fewer studies have addressed the effects of T cell activation on central nervous system (CNS) function. The discovery and characterization of bacterial superantigens (SAgs) has introduced an important opportunity for studying how T cell activation influences CNS function. Superantigens target unique variable regions of the beta chain of the mouse and human T cell receptor. This is restricted by the class II molecule of the major histocompatibility complex (MHC), and results in the production of a cytokine cascade thatincludes interleukin-2 (IL-2), interferon-gamma (IFNgamma), tumor necrosis factor (TNF) and many other cytokines, including IL-6. The best studied SAgs are the staphylococcal enterotoxins, of which staphylococcal enterotoxins A and B (SEA and SEB), have been shown to produce significant changes in behavior and activation of the hypothalamic-pituitary-adrenal (HPA) axis. Importantly, a T cell requirement was necessary to produce these changes. Furthermore, the anorexic or hypophagic effects of SAg challenge in mice appears to be related to anxiety-like processes, since challenge with both SEA or SEB reduces consumption of mainly novel food or food presented in a novel context. In the present paper, these studies are reviewed and related to known alterations in both anxiogenic and anxiolytic neuropeptides. It is suggested that immunologically-induced changes in the brain activate both categories of neuropeptides, thereby sustaining an adaptive state of arousal that promotes appropriate behavioral adjustments during infectious illness.
机译:免疫反应代表全身压力的来源,它会影响大脑并改变各种神经内分泌和行为功能。因此,人们认为免疫系统是压力相关行为异常(如抑郁症)的潜在贡献者。通过主要集中于针对天然免疫细胞(例如巨噬细胞)的细胞因子和/或细菌内毒素(例如LPS)的管理研究,已经获得了许多此类知识。但是,很少有研究针对T细胞活化对中枢神经系统(CNS)功能的影响。细菌超抗原(SAgs)的发现和表征为研究T细胞活化如何影响CNS功能提供了重要的机会。超抗原靶向小鼠和人类T细胞受体β链的独特可变区。这受到主要组织相容性复合物(MHC)的II类分子的限制,并导致产生细胞因子级联反应,包括白介素2(IL-2),干扰素-γ(IFNgamma),肿瘤坏死因子(TNF)和许多其他细胞因子,包括IL-6。研究最好的SAg是葡萄球菌肠毒素,其中的葡萄球菌肠毒素A和B(SEA和SEB)已显示出行为和激活下丘脑-垂体-肾上腺(HPA)轴的显着变化。重要的是,必须要有T细胞才能产生这些变化。此外,SAg激发在小鼠中的厌食或吞咽作用似乎与焦虑样过程有关,因为用SEA或SEB激发都减少了主要食用新颖食物或出现在新颖环境中的食物的消耗。在本文中,对这些研究进行了综述,并与已知的抗焦虑和抗焦虑神经肽改变有关。有人认为,免疫学上引起的大脑变化激活了两种神经肽,从而维持了一种适应性的唤醒状态,从而在传染病期间促进了适当的行为调节。

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