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高脂饮食诱导的肥胖导致肠道 Th17/Treg 失衡,损害肠道屏障,并加重小鼠的焦虑样行为。

High-fat diet-induced obesity causes intestinal Th17/Treg imbalance that impairs the intestinal barrier and aggravates anxiety-like behavior in mice.

机构信息

Department of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou 510655, China; Biomedical Innovation Center, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou 510530, China.

Department of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou 510655, China; Biomedical Innovation Center, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou 510530, China.

出版信息

Int Immunopharmacol. 2024 Mar 30;130:111783. doi: 10.1016/j.intimp.2024.111783. Epub 2024 Mar 7.

Abstract

The prevalence of autism spectrum disorders (ASD) has been steadily increasing, and growing evidence suggests a link between high-fat diet (HFD), obesity, and ASD; however, the mechanism underlying this association remains elusive. Herein, BTBR T + tf/J (BTBR) inbred mice (a mouse ASD model) and C57Bl/6J (C57) mice were fed an HFD and normal diet (ND) for 8 weeks (groups: C57 + ND, C57 + HFD, BTBR + ND, and BTBR + HFD). Subsequently, mice underwent behavioral assessments, followed by intestinal tissues harvesting to detect expression of intestinal barrier proteins and inflammatory factors and immune cell numbers, and a correlation analysis. HFD-fed BTBR mice developed obesity, elevated blood sugar, significantly aggravated anxiety-like behaviors, impaired intestinal barrier function, intestinal inflammation with elevated CD4IL17 T (Th17) cells and reduced CD4Foxp3 T (Treg) cells, exhibiting reduced expression of proteins related to AMPK regulatory pathway (AMPK, p-AMPK, SIRT1). Correlation analysis revealed that the degree of behavioral anxiety, the degree of intestinal barrier damage, the severity of intestinal inflammation, and the degree of immune cell imbalance positively correlated with each other. Accordingly, HFD-induced obesity may cause intestinal Th17/Treg imbalance via the AMPK-SIRT1 pathway, leading to an inflammatory environment in the intestine, impairing intestinal barrier function, and ultimately aggravating anxiety-like behaviors in mice.

摘要

自闭症谱系障碍 (ASD) 的患病率一直在稳步上升,越来越多的证据表明高脂肪饮食 (HFD)、肥胖症和 ASD 之间存在关联;然而,这种关联的机制仍不清楚。在此,我们使用 BTBR T + tf / J(BTBR)近交系小鼠(一种 ASD 模型小鼠)和 C57Bl/6J(C57)小鼠进行了 8 周的高脂肪饮食和正常饮食喂养(分组:C57 + ND、C57 + HFD、BTBR + ND 和 BTBR + HFD)。随后,对小鼠进行行为评估,然后采集肠道组织以检测肠道屏障蛋白和炎症因子以及免疫细胞数量的表达,并进行相关性分析。HFD 喂养的 BTBR 小鼠出现肥胖、血糖升高、焦虑样行为明显加重、肠道屏障功能受损、肠道炎症伴 CD4IL17 T(Th17)细胞升高和 CD4Foxp3 T(Treg)细胞减少,表现出与 AMPK 调节通路(AMPK、p-AMPK、SIRT1)相关的蛋白表达减少。相关性分析显示,行为焦虑程度、肠道屏障损伤程度、肠道炎症严重程度和免疫细胞失衡程度相互之间呈正相关。因此,HFD 诱导的肥胖可能通过 AMPK-SIRT1 通路引起肠道 Th17/Treg 失衡,导致肠道炎症环境,损害肠道屏障功能,并最终加重小鼠的焦虑样行为。

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