Department of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Antioxid Redox Signal. 2011 Oct 1;15(7):1779-88. doi: 10.1089/ars.2010.3722. Epub 2011 Apr 11.
Diabetes exacerbates ischemic heart disease morbidity and mortality via incompletely understood mechanisms. Although adiponectin (APN) reduces myocardial ischemia/reperfusion (MI/R) injury in nondiabetic animals, whether APN's cardioprotective actions are altered in diabetes, a pathologic condition with endogenously reduced APN, has never been investigated. High-fat diet (HD)-induced diabetic mice and normal diet (ND) controls were subjected to MI via coronary artery ligation, and given vehicle or APN globular domain (gAPN, 2 μg/g) 10 min before reperfusion. Compared to ND mice (where gAPN exerted pronounced cardioprotection), HD mice manifested greater MI/R injury, and a tripled gAPN dose was requisite to achieve cardioprotective extent seen in ND mice (i.e., infarct size, apoptosis, and cardiac function). APN reduces MI/R injury via AMP-activated protein kinase (AMPK)-dependent metabolic regulation and AMPK-independent antioxidative/antinitrative pathways. Compared to ND, HD mice manifested significantly blunted gAPN-induced AMPK activation, basally and after MI/R (p<0.05). Although both low- and high-dose gAPN equally attenuated MI/R-induced oxidative stress (i.e., NADPH oxidase expression and superoxide production) and nitrative stress (i.e., inducible nitric oxide synthase expression, nitric oxide production, and peroxynitrite formation) in ND mice, only high-dose gAPN efficaciously did so in HD mice. We demonstrate for the first time that HD-induced diabetes diminished both AMPK-dependent and AMPK-independent APN cardioprotection, suggesting an unreported diabetic heart APN resistance.
糖尿病通过尚未完全阐明的机制加重缺血性心脏病的发病率和死亡率。虽然脂联素 (APN) 可减轻非糖尿病动物的心肌缺血/再灌注 (MI/R) 损伤,但在糖尿病状态下,APN 的心脏保护作用是否会改变,这种病理状态下内源性 APN 减少,尚未得到研究。通过冠状动脉结扎使高脂肪饮食 (HD) 诱导的糖尿病小鼠和正常饮食 (ND) 对照组发生 MI,并在再灌注前 10 分钟给予载体或 APN 球状结构域 (gAPN,2μg/g)。与 ND 小鼠相比 (gAPN 在此处表现出明显的心脏保护作用),HD 小鼠表现出更大的 MI/R 损伤,需要增加三倍的 gAPN 剂量才能达到 ND 小鼠中观察到的心脏保护程度 (即梗死面积、凋亡和心脏功能)。APN 通过 AMP 激活的蛋白激酶 (AMPK) 依赖性代谢调节和 AMPK 非依赖性抗氧化/抗硝化途径来减轻 MI/R 损伤。与 ND 相比,HD 小鼠表现出 gAPN 诱导的 AMPK 激活明显减弱,基础状态和 MI/R 后均如此 (p<0.05)。尽管低剂量和高剂量 gAPN 均能同等程度地减轻 ND 小鼠的 MI/R 诱导的氧化应激 (即 NADPH 氧化酶表达和超氧产生) 和硝化应激 (即诱导型一氧化氮合酶表达、一氧化氮产生和过氧亚硝酸盐形成),但只有高剂量 gAPN 在 HD 小鼠中才有效。我们首次证明,HD 诱导的糖尿病降低了 AMPK 依赖性和 AMPK 非依赖性 APN 的心脏保护作用,提示存在一种未被报道的糖尿病心脏 APN 抵抗。