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长期高脂饮食会加重对小型隐匿性缺血性中风的细胞反应。

Prolonged High Fat Diet Worsens the Cellular Response to a Small, Covert-like Ischemic Stroke.

机构信息

Division of BioMedical Sciences, Memorial University, 300 Prince Philip Drive, St. John's, NL, Canada, A1B 3V6.

Division of BioMedical Sciences, Memorial University, 300 Prince Philip Drive, St. John's, NL, Canada, A1B 3V6.

出版信息

Neuroscience. 2019 May 15;406:637-652. doi: 10.1016/j.neuroscience.2019.01.050. Epub 2019 Feb 4.

DOI:10.1016/j.neuroscience.2019.01.050
PMID:30731155
Abstract

Obesity is associated with worse neurological outcomes following overt ischemic strokes. The majority of strokes however, are covert, small strokes that often evade detection. How obesity impacts the cellular response to covert strokes is unclear. Here, we used a diet-induced obesity model by feeding mice a high fat diet (HFD) and examining its impact on the behavioral and cellular responses to either an Endothelin-1-induced focal ischemic stroke or a saline injection (control). Specifically, we examined cells in regions with different levels of blood perfusion: the non-perfused core, the hypo-perfused surround and the perfused region around the infarct. We show that HFD selectively exacerbated the response to stroke but not to saline injections. Stroke affected the composition of microglia/macrophages, astrocytes and neurons within each region of perfusion. In the non-perfused core, the majority of cells were Iba-1+ microglia and macrophages. HFD resulted in a greater infiltration of CD68+ macrophages into the infarct core while CD68+ /TMEM119+ microglia were reduced. Furthermore, there was a trend towards an increased spread of the astrogliosis scar from the infarct border in the HFD condition. Within the hypo-perfused region, significantly fewer neurons survived in HFD-fed mice than Chow-fed mice, suggesting that neurons in the HFD condition have an increased vulnerability. In summary, diet-induced obesity exacerbates covert-like stroke injuries by worsening the cellular responses in the varying levels of perfusion across the infarct.

摘要

肥胖与明显缺血性中风后神经功能恶化有关。然而,大多数中风是隐匿性的小中风,往往难以察觉。肥胖对隐匿性中风后细胞反应的影响尚不清楚。在这里,我们使用高脂肪饮食(HFD)喂养小鼠的饮食诱导肥胖模型,研究其对内皮素-1诱导的局灶性缺血性中风或盐水注射(对照)后行为和细胞反应的影响。具体来说,我们检查了具有不同血流灌注水平的区域中的细胞:未灌注核心、低灌注周围和梗塞周围的灌注区域。我们发现 HFD 选择性地加剧了对中风的反应,但对盐水注射没有影响。中风影响了每个灌注区域中小胶质细胞/巨噬细胞、星形胶质细胞和神经元的组成。在未灌注核心中,大多数细胞是 Iba-1+小胶质细胞和巨噬细胞。HFD 导致 CD68+巨噬细胞更多地浸润梗塞核心,而 CD68+ / TMEM119+小胶质细胞减少。此外,在 HFD 条件下,星形胶质细胞瘢痕从梗塞边界的扩散有增加的趋势。在低灌注区域,HFD 喂养的小鼠中存活的神经元明显少于 Chow 喂养的小鼠,这表明 HFD 条件下的神经元更易受损。总之,饮食诱导的肥胖通过加重梗塞区域不同血流灌注水平的细胞反应,加剧了隐匿性样中风损伤。

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