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对老年小鼠进行褪黑素治疗可使大脑对脂多糖产生更年轻化的反应。

Melatonin treatment in old mice enables a more youthful response to LPS in the brain.

作者信息

Perreau V M, Bondy S C, Cotman C W, Sharman K G, Sharman E H

机构信息

Institute for Brain Aging and Dementia, USA.

出版信息

J Neuroimmunol. 2007 Jan;182(1-2):22-31. doi: 10.1016/j.jneuroim.2006.09.005. Epub 2006 Oct 30.

Abstract

Melatonin modulates the expression of a number of genes related to inflammation and immunity. Declining levels of melatonin with age may thus relate to some of the changes in immune function that occur with age. mRNA expression levels in murine CNS were measured using oligonucleotide microarrays in order to determine whether a dietary melatonin supplement may modify age-related changes in the response to an inflammatory challenge. CB6F1 male mice were fed 40-ppm melatonin for 9 weeks prior to sacrifice at 26.5 months of age, and compared with age-matched untreated controls and 4.5-month-old controls. A subset of both young and old animals was injected i.p. with lipopolysaccharide (LPS). After 3 h, total RNA was extracted from whole brain (excluding brain stem and cerebellum), and individual samples were hybridized to Affymetrix Mouse 430-2.0 arrays. Data were analyzed in Dchip and GeneSpring. Melatonin treatment markedly altered the response in gene expression of older animals subjected to an LPS challenge. These changes in general, caused the response to more closely resemble that of young animals subjected to the same LPS challenge. Thus melatonin treatment effects a major shift in the response of the CNS to an inflammatory challenge, causing a transition to a more youthful mRNA expression profile.

摘要

褪黑素可调节许多与炎症和免疫相关的基因的表达。因此,随着年龄增长褪黑素水平的下降可能与免疫功能随年龄发生的一些变化有关。为了确定膳食补充褪黑素是否可以改变对炎症刺激的反应中与年龄相关的变化,使用寡核苷酸微阵列测量了小鼠中枢神经系统中的mRNA表达水平。在26.5月龄处死前,给CB6F1雄性小鼠喂食40ppm的褪黑素9周,并与年龄匹配的未处理对照和4.5月龄对照进行比较。对年轻和老年动物的一个亚组腹腔注射脂多糖(LPS)。3小时后,从全脑(不包括脑干和小脑)中提取总RNA,并将单个样品与Affymetrix Mouse 430-2.0阵列杂交。在Dchip和GeneSpring中分析数据。褪黑素处理显著改变了接受LPS刺激的老年动物的基因表达反应。总体而言,这些变化使反应更类似于接受相同LPS刺激的年轻动物的反应。因此,褪黑素处理使中枢神经系统对炎症刺激的反应发生了重大转变,导致向更年轻的mRNA表达谱转变。

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