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阿尔茨海默病非裔美国人脑组织 BA21 中炎症增加。

Increased inflammation in BA21 brain tissue from African Americans with Alzheimer's disease.

机构信息

Division of Neurotoxicology, National Center for Toxicological Research/Food and Drug Administration, 3900 NCTR Road, Jefferson, AR, 72079, USA.

Division of Systems Biology, National Center for Toxicological Research/Food and Drug Administration, Jefferson, AR, 72079, USA.

出版信息

Metab Brain Dis. 2020 Jan;35(1):121-133. doi: 10.1007/s11011-019-00512-2. Epub 2019 Dec 10.

Abstract

Chronic neuroinflammation is strongly associated with AD and altered peripheral and central levels of chemokines and cytokines have been frequently described in those with AD. Given the increasing evidence of ethnicity-related differences in AD, it was of interest to determine if those altered chemokine and cytokine levels are ethnicity-related. Because African Americans exhibit a higher incidence of AD and increased symptom severity, we explored chemokine and cytokine concentrations in post-mortem brain tissue from the BA21 region of African Americans and Caucasians with AD using multiplex assays. IL-1β, MIG, TRAIL, and FADD levels were significantly increased in African Americans while levels of IL-3 and IL-8 were significantly decreased. Those effects did not interact with gender; however, overall levels of CCL25, CCL26 and CX3CL1 were significantly decreased in women. The NLRP3 inflammasome is thought to be critically involved in AD. Increased activation of this inflammasome in African Americans is consistent with the current results.

摘要

慢性神经炎症与 AD 密切相关,在 AD 患者中经常描述外周和中枢水平的趋化因子和细胞因子发生改变。鉴于 AD 与种族相关差异的证据不断增加,因此确定这些趋化因子和细胞因子水平是否与种族相关是很有意义的。由于非裔美国人患 AD 的发病率更高,且症状严重程度增加,我们使用多重分析方法探索了 AD 患者死后大脑组织 BA21 区域中非裔美国人和高加索人趋化因子和细胞因子的浓度。IL-1β、MIG、TRAIL 和 FADD 的水平在非裔美国人中显著升高,而 IL-3 和 IL-8 的水平则显著降低。这些影响与性别没有相互作用;然而,女性 CCL25、CCL26 和 CX3CL1 的总体水平显著降低。NLRP3 炎性小体被认为在 AD 中起着至关重要的作用。非裔美国人中这种炎性小体的激活增加与目前的结果一致。

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