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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >MULTIPLE LIPOPOLYSACCHARIDE (LPS) INJECTIONS ALTER INTERLEUKIN 6 (IL-6), IL-7, IL-10 AND IL-6 AND IL-7 RECEPTOR MRNA IN CNS AND SPLEEN
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MULTIPLE LIPOPOLYSACCHARIDE (LPS) INJECTIONS ALTER INTERLEUKIN 6 (IL-6), IL-7, IL-10 AND IL-6 AND IL-7 RECEPTOR MRNA IN CNS AND SPLEEN

机译:多种脂多糖(LPS)注射在CNS和脾脏中改变白细胞介素6(IL-6),IL-7,IL-10和IL-6和IL-7受体mRNA

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Neuroinflammation is proposed to be an important component in the development of several central nervous system (CNS) disorders including depression, Alzheimer's disease, Parkinson's disease, and traumatic brain injury. However, exactly how neuroinflammation leads to, or contributes to, these central disorders is unclear. The objective of the study was to examine and compare the expression of mRNAs for interleukin-6 (IL-6), IL-7, IL-10 and the receptors for IL-6 (IL-6R) and IL-7 (IL-7R) using in situ hybridization in discrete brain regions and in the spleen after multiple injections of 3 mg/kg lipopolysaccharide (LPS), a model of neuroinflammation. In the spleen, LPS significantly elevated IL-6 mRNA expression, then IL-10 mRNA, with no effect on IL-7 or IL-7R mRNA, while significantly decreasing IL-6R mRNA expression. In the CNS, LPS administration had the greatest effect on IL-6 and IL-6R mRNA. LPS increased IL-6 mRNA expression only in non neuronal cells throughout the brain, but significantly elevated IL-6R mRNA in neuronal populations, where observed, except the cerebellum. LPS resulted in variable effects on IL-10 mRNA, and had no effect on IL-7 or IL-7R mRNA expression. These studies indicate that LPS-induced neuroinflammation has substantial but variable effects on the regional and cellular patterns of CNS IL-6, IL-7 and IL-10, and for IL-6R and IL-7R mRNA expression. It is apparent that administration of LPS can affect non-neuronal and neuronal cells in the brain. Further research is required to determine how CNS inflammatory changes associated with IL-6, IL-10 and IL-6R could in turn contribute to the development of CNS neurological disorders. Published by Elsevier Ltd on behalf of IBRO.
机译:提出神经源性炎症是在若干中枢神经系统(CNS)疾病的发展中的重要组成部分,包括抑郁症,阿尔茨海默病,帕金森病和创伤性脑损伤。然而,究竟是如何使神经引起的炎症如何导致或有助于这些中枢紊乱尚不清楚。该研究的目的是检查和比较IL-6(IL-6R)和IL-7(IL-)的白细胞介素-6(IL-6),IL-7,IL-10和受体的MRNA的表达(IL-7)(IL- 7R)在分立脑区中使用原位杂交和在脾脏中的3mg / kg脂多糖(LPS)中的脾脏中,是神经引发模型。在脾脏中,LPS显着升高IL-6 mRNA表达,然后是IL-10 mRNA,对IL-7或IL-7R mRNA没有影响,同时显着降低IL-6R mRNA表达。在CNS中,LPS施用对IL-6和IL-6R mRNA具有最大的影响。 LPS仅在整个脑中的非神经元细胞中增加IL-6 mRNA表达,但除了小脑外,观察到的神经元群体中的IL-6R mRNA显着升高。 LPS导致IL-10 mRNA导致可变效应,对IL-7或IL-7R mRNA表达没有影响。这些研究表明,LPS诱导的神经炎性对CNS IL-6,IL-7和IL-10的区域和细胞图案具有重要但可变的影响,以及IL-6R和IL-7R mRNA表达。显然,LPS的给药可以影响大脑中的非神经元和神经元细胞。需要进一步的研究来确定与IL-6,IL-10和IL-6R相关的CNS炎症变化又有助于CNS神经系统疾病的发育。由elsevier有限公司代表银布发布。

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