Department of Anesthesiology, Pharmacology and Therapeutics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Clin Endocrinol (Oxf). 2011 Jun;74(6):705-13. doi: 10.1111/j.1365-2265.2011.03979.x.
Patients with diabetes experience increased cardiovascular complications after cardiac surgery. Hyperglycaemia predicts increased mortality after myocardial infarction and may influence cardiovascular risk in humans. Impaired prosurvival phosphatase and tensin homologue on chromosome 10 (PTEN)-Akt signalling could be an important feature of the diabetic heart rendering it resistant to preconditioning. This study was designed to evaluate for differences and relationships of myocardial PTEN-Akt-related signalling and baseline glycaemic control marker in type 2 diabetic and nondiabetic patients undergoing coronary artery bypass surgery.
Right atrial biopsies and coronary sinus blood were obtained from 18 type 2 diabetic and 18 nondiabetic patients intraoperatively. Expression and phosphorylation of Akt, endothelial nitric oxide synthase (eNOS), Bcl-2 and PTEN were evaluated by Western blot. Plasma 15-F(2t) -isoprostane concentrations were evaluated by liquid chromatography-mass spectrometry.
PTEN expression and 15-F(2t) -isoprostane concentrations were significantly higher in diabetic patients. Increased fasting blood glucose levels correlated with increased coronary sinus plasma 15-F(2t) -isoprostane concentrations. Increased cardiac 15-F(2t) -isoprostane generation was highly correlated with myocardial PTEN expression. Bcl-2 expression and eNOS phosphorylation were significantly lower in diabetic compared with nondiabetic patients. Akt phosphorylation tended to be lower in diabetic patients; however, this tendency failed to reach statistical significance.
The current results suggest that prosurvival PTEN-Akt signalling is impaired in the diseased diabetic myocardium. Hyperglycaemia and increased oxidative stress may contribute to this phenomenon. These findings strengthen the understanding of the underlying biologic mechanisms of cardiac injury in diabetic patients, which could facilitate development of new treatments to prevent cardiovascular complications in this high-risk population.
糖尿病患者在心脏手术后会经历增加的心血管并发症。高血糖预测心肌梗死后的死亡率增加,并且可能影响人类的心血管风险。受损的生存促进磷酸酶和张力蛋白同源物 on chromosome 10 (PTEN)-Akt 信号可能是糖尿病心脏的一个重要特征,使其对预处理有抗性。本研究旨在评估 2 型糖尿病和非糖尿病患者在接受冠状动脉旁路手术后心肌 PTEN-Akt 相关信号和基线血糖控制标志物的差异和关系。
术中从 18 例 2 型糖尿病患者和 18 例非糖尿病患者中获取右心房活检和冠状窦血。通过 Western blot 评估 Akt、内皮型一氧化氮合酶 (eNOS)、Bcl-2 和 PTEN 的表达和磷酸化。通过液相色谱-质谱法评估血浆 15-F(2t)-isoprostane 浓度。
糖尿病患者的 PTEN 表达和 15-F(2t)-isoprostane 浓度显著升高。空腹血糖水平升高与冠状窦血浆 15-F(2t)-isoprostane 浓度升高相关。增加的心脏 15-F(2t)-isoprostane 生成与心肌 PTEN 表达高度相关。与非糖尿病患者相比,糖尿病患者的 Bcl-2 表达和 eNOS 磷酸化显著降低。Akt 磷酸化在糖尿病患者中倾向于降低;然而,这种趋势未达到统计学意义。
目前的结果表明,在患病的糖尿病心肌中,生存促进的 PTEN-Akt 信号受损。高血糖和增加的氧化应激可能导致这种现象。这些发现加强了对糖尿病患者心脏损伤潜在生物学机制的理解,这可能有助于开发新的治疗方法来预防这一高危人群的心血管并发症。