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高脂饮食喂养的小鼠中髓系沉默调节蛋白 1 缺乏加重海马炎症。

Myeloid sirtuin1 deficiency aggravates hippocampal inflammation in mice fed high-fat diets.

机构信息

Department of Anatomy and Convergence Medical Science, Bio Anti-aging Medical Research Center, Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju, Gyeongnam 52727, Republic of Korea.

Department of Thoracic and Cardiovascular Surgery, Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju, Gyeongnam 52727, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2018 May 23;499(4):1025-1031. doi: 10.1016/j.bbrc.2018.04.044. Epub 2018 Apr 10.

Abstract

Chronic low-grade inflammation-induced insulin resistance is associated with neuroinflammation. Myeloid sirtuin1 (SIRT1) deficiency aggravates high-fat diet (HFD)-induced insulin resistance. However, the function of myeloid-specific SIRT1 in the hippocampus of obese mice is largely unknown. To address this question, we fed myeloid SIRT1 knockout (KO) mice a HFD for 40 weeks. We found that HFD-fed SIRT1 KO mice had increased insulin resistance and macrophage infiltration in adipose tissue than wild type (WT) mice. Levels of HFD-induced lipocalin-2 (LCN2) were lower in SIRT1 KO mice than in WT. HFD-induced hippocampal LCN2 expression was lower in HFD-fed SIRT1 KO mice than in WT. Hippocampal acetylation of nuclear factor-κB (NF-κB) and amyloid precursor protein levels were higher in HFD-fed SIRT1 KO mice than in HFD-fed WT mice. Taken together, our results suggest that targeted induction of the anti-inflammatory effects of SIRT1 and LCN2 may help prevent obesity-associated insulin resistance and neuroinflammation.

摘要

慢性低度炎症引起的胰岛素抵抗与神经炎症有关。髓系沉默信息调节因子 1(SIRT1)缺乏会加重高脂肪饮食(HFD)诱导的胰岛素抵抗。然而,肥胖小鼠海马中髓系特异性 SIRT1 的功能在很大程度上是未知的。为了解决这个问题,我们用高脂肪饮食喂养髓系 SIRT1 敲除(KO)小鼠 40 周。我们发现,与野生型(WT)小鼠相比,高脂肪饮食喂养的 SIRT1 KO 小鼠表现出更高的胰岛素抵抗和脂肪组织中巨噬细胞浸润。SIRT1 KO 小鼠中高脂肪饮食诱导的脂联素 2(LCN2)水平低于 WT 小鼠。与 WT 小鼠相比,高脂肪饮食喂养的 SIRT1 KO 小鼠海马中 LCN2 的表达也较低。与高脂肪饮食喂养的 WT 小鼠相比,SIRT1 KO 小鼠海马中核因子-κB(NF-κB)的乙酰化和淀粉样前体蛋白水平更高。综上所述,我们的结果表明,靶向诱导 SIRT1 和 LCN2 的抗炎作用可能有助于预防肥胖相关的胰岛素抵抗和神经炎症。

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