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Globular adiponectin ameliorates metabolic insulin resistance via AMPK-mediated restoration of microvascular insulin responses

机译:球状脂联素通过AMPK介导的微血管胰岛素反应的恢复改善代谢性胰岛素抵抗

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Hypoadiponectinaemia is closely associated with endothelial dysfunction and insulin resistance, and microvasculature plays a critical role in the regulation of insulin action in muscle. Here we tested whether adiponectin replenishment could improve metabolic insulin sensitivity in male rats fed a high-fat diet (HFD) via the modulation of microvascular insulin responses. Male Sprague-Dawley rats were fed either a HFD or low-fat diet (LFD) for 4weeks. Small resistance artery myograph changes in tension, muscle microvascular recruitment and metabolic response to insulin were determined. Compared with rats fed a LFD, HFD feeding abolished the vasodilatory actions of globular adiponectin (gAd) and insulin on pre-constricted distal saphenous arteries. Pretreatment with gAd improved insulin responses in arterioles isolated from HFD rats, which was blocked by AMP-activated protein kinase (AMPK) inhibition. Similarly, HFD abolished microvascular responses to either gAd or insulin and decreased insulin-stimulated glucose disposal by approximate to 60%. However, supplementing gAd fully rescued insulin's microvascular action and significantly improved the metabolic responses to insulin in HFD male rats and these actions were abolished by inhibition of either AMPK or nitric oxide production. We conclude that HFD induces vascular adiponectin and insulin resistance but gAd administration can restore vascular insulin responses and improve insulin's metabolic action via an AMPK- and nitric oxide-dependent mechanism in male rats.
机译:低脂连蛋白血症与内皮功能障碍和胰岛素抵抗密切相关,并且微脉管系统在肌肉中胰岛素作用的调节中起关键作用。在这里,我们测试了脂联素的补充是否可以通过调节微血管胰岛素反应来改善高脂饮食(HFD)喂养的雄性大鼠的代谢胰岛素敏感性。给雄性Sprague-Dawley大鼠喂食HFD或低脂饮食(LFD)4周。确定了小阻力动脉肌电图在张力,肌肉微血管募集和对胰岛素的代谢反应方面的变化。与饲喂LFD的大鼠相比,饲喂HFD的大鼠消除了球状脂联素(gAd)和胰岛素对预收缩远端隐性动脉的血管舒张作用。用gAd预处理可改善从HFD大鼠分离出的小动脉中的胰岛素反应,该反应被AMP激活的蛋白激酶(AMPK)抑制所阻断。同样,HFD消除了对gAd或胰岛素的微血管反应,并使胰岛素刺激的葡萄糖处置减少了约60%。然而,补充gAd可以完全拯救胰岛素在HFD雄性大鼠中的微血管作用,并显着改善其对胰岛素的代谢反应,而这些作用由于抑制AMPK或一氧化氮的产生而被取消。我们得出的结论是,HFD诱导血管脂联素和胰岛素抵抗,但gAd给药可以通过AMPK和一氧化氮依赖性机制在雄性大鼠中恢复血管胰岛素反应并改善胰岛素的代谢作用。

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