Division of Endocrinology and Metabolism, Department of Medicine, University of Virginia Health System, Charlottesville, VA.
Diabetes. 2023 Jul 1;72(7):918-931. doi: 10.2337/db22-0745.
Inflammation-induced vascular insulin resistance is an early event in diet-induced obesity and contributes to metabolic insulin resistance. To examine whether exercise and glucagon-like peptide 1 (GLP-1) receptor agonism, alone or in combination, modulate vascular and metabolic insulin actions during obesity development, we performed a euglycemic insulin clamp in adult male rats after 2 weeks of high-fat diet feeding with either access to a running wheel (exercise), liraglutide, or both. Rats exhibited increased visceral adiposity and blunted microvascular and metabolic insulin responses. Exercise and liraglutide alone each improved muscle insulin sensitivity, but their combination fully restored insulin-mediated glucose disposal rates. The combined exercise and liraglutide intervention enhanced insulin-mediated muscle microvascular perfusion, reduced perivascular macrophage accumulation and superoxide production in the muscle, attenuated blood vessel inflammation, and improved endothelial function, along with increasing endothelial nucleus translocation of NRF2 and increasing endothelial AMPK phosphorylation. We conclude that exercise and liraglutide synergistically enhance the metabolic actions of insulin and reduce vascular oxidative stress and inflammation in the early stage of obesity development. Our data suggest that early combination use of exercise and GLP-1 receptor agonism might be an effective strategy in preventing vascular and metabolic insulin resistance and associated complications during the development of obesity.
Inflammation-induced vascular insulin resistance occurs early in diet-induced obesity and contributes to metabolic insulin resistance. We examined whether exercise and GLP-1 receptor agonism, alone or in combination, modulate vascular and metabolic insulin actions during obesity development. We found that exercise and liraglutide synergistically enhanced the metabolic actions of insulin and reduced perimicrovascular macrophage accumulation, vascular oxidative stress, and inflammation in the early stage of obesity development. Our data suggest that early combination use of exercise and a GLP-1 receptor agonist might be an effective strategy in preventing vascular and metabolic insulin resistance and associated complications during the development of obesity.
炎症引起的血管胰岛素抵抗是饮食诱导肥胖的早期事件,并导致代谢性胰岛素抵抗。为了研究运动和胰高血糖素样肽 1(GLP-1)受体激动剂单独或联合使用是否在肥胖发展过程中调节血管和代谢胰岛素作用,我们在高脂饮食喂养 2 周后,对成年雄性大鼠进行了正葡萄糖胰岛素钳夹,这些大鼠可以使用跑步轮(运动)、利拉鲁肽或两者兼用。大鼠表现出内脏脂肪增加和微血管及代谢胰岛素反应减弱。运动和利拉鲁肽单独使用均可改善肌肉胰岛素敏感性,但两者联合使用可完全恢复胰岛素介导的葡萄糖清除率。联合运动和利拉鲁肽干预增强了胰岛素介导的肌肉微血管灌注,减少了肌肉中的血管周围巨噬细胞积累和超氧化物产生,减轻了血管炎症,改善了内皮功能,同时增加了内皮核中 NRF2 的易位和内皮 AMPK 的磷酸化。我们得出结论,运动和利拉鲁肽协同增强了胰岛素的代谢作用,并在肥胖发展的早期阶段降低了血管的氧化应激和炎症。我们的数据表明,早期联合使用运动和 GLP-1 受体激动剂可能是预防肥胖发展过程中血管和代谢性胰岛素抵抗及相关并发症的有效策略。