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AMPK 激活可减轻炎症反应,从而降低健康和糖尿病小鼠对环境 PM 引起的代谢紊乱。

AMPK activation attenuates inflammatory response to reduce ambient PM-induced metabolic disorders in healthy and diabetic mice.

机构信息

Department of Environmental Health, School of Public Health and the Key Laboratory of Public Health Safety, Ministry of Education, Fudan University, Shanghai, China.

Shanghai Key Laboratory of Meteorology and Health, Shanghai, China.

出版信息

Ecotoxicol Environ Saf. 2019 Sep 15;179:290-300. doi: 10.1016/j.ecoenv.2019.04.038. Epub 2019 May 6.

Abstract

Epidemiological and experimental studies have indicated that ambient fine particulate matter (PM) exposure is associated with the occurrence and development of metabolic disorders such as obesity and type 2 diabetes mellitus (T2DM). However, the mechanism is not clear yet, and there are few studies to explore the possible prevention measure. In this study, C57BL/6 and db/db mice were exposed to concentrated PM or filtered air using Shanghai Meteorological and Environmental Animal Exposure System (Shanghai-METAS) for 12 weeks. From week 11, some of the mice were assigned to receive a subcutaneous injection of AMPK activator (AICAR). Lipid metabolism, glucose tolerance, insulin sensitivity and energy homeostasis were measured. Meanwhile, the respiratory, systemic and visceral fat inflammatory response was detected. The results showed that PM exposure induced the impairments of glucose tolerance, insulin resistance, lipid metabolism disorders and disturbances of energy metabolism in both C57BL/6 and db/db mice. These impairments might be consistent with the increased respiratory, circulating and visceral adipose tissue (VAT) inflammatory response, which was characterized by the release of IL-6 and TNF-α in lung, serum and VAT. More importantly, AICAR administration led to the significant enhancement of energy metabolism, elevation of AMPK as well as the decreased IL-6 and TNF-α in VAT of PM-exposed mice, which suggesting that AMPK activation might attenuate the inflammatory responses in VAT via the inhibition of MAPKs and NFκB. The study indicated that exposure to ambient PM under the concentration which is often seen in some developing countries could induce the occurrence of metabolic disorders in normal healthy mice and exacerbate metabolic disorders in diabetic mice. The adverse impacts of PM on insulin sensitivity, energy homeostasis, lipid metabolism and inflammatory response were associated with AMPK inhibition. AMPK activation might inhibit PM-induced metabolic disorders via inhibition of inflammatory cytokines release. These findings suggested that AMPK activation is a potential therapy to prevent some of the metabolic disorders attributable to air pollution exposure.

摘要

流行病学和实验研究表明,环境细颗粒物(PM)暴露与肥胖和 2 型糖尿病(T2DM)等代谢紊乱的发生和发展有关。然而,其机制尚不清楚,且很少有研究探索可能的预防措施。在这项研究中,使用上海气象环境动物暴露系统(Shanghai-METAS)使 C57BL/6 和 db/db 小鼠暴露于浓缩 PM 或过滤空气中 12 周。从第 11 周开始,一些小鼠被分配接受 AMPK 激活剂(AICAR)的皮下注射。测量脂质代谢、葡萄糖耐量、胰岛素敏感性和能量平衡。同时,检测呼吸、全身和内脏脂肪炎症反应。结果表明,PM 暴露导致 C57BL/6 和 db/db 小鼠的葡萄糖耐量受损、胰岛素抵抗、脂质代谢紊乱和能量代谢紊乱。这些损伤可能与呼吸、循环和内脏脂肪组织(VAT)炎症反应的增加一致,其特征是肺、血清和 VAT 中释放白细胞介素 6(IL-6)和肿瘤坏死因子-α(TNF-α)。更重要的是,AICAR 给药导致 PM 暴露小鼠的能量代谢显著增强、AMPK 升高以及 VAT 中 IL-6 和 TNF-α 降低,这表明 AMPK 激活可能通过抑制 MAPKs 和 NFκB 来减轻 VAT 中的炎症反应。该研究表明,在一些发展中国家经常出现的浓度下暴露于环境 PM 可导致正常健康小鼠发生代谢紊乱,并使糖尿病小鼠的代谢紊乱恶化。PM 对胰岛素敏感性、能量平衡、脂质代谢和炎症反应的不利影响与 AMPK 抑制有关。AMPK 激活可能通过抑制炎症细胞因子的释放来抑制 PM 诱导的代谢紊乱。这些发现表明,AMPK 激活是预防一些归因于空气污染暴露的代谢紊乱的潜在疗法。

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