Otago School of Medical Sciences, Department of Physiology and HeartOtago, University of Otago, 270 Great King Street, Dunedin, 9016, New Zealand.
Otago School of Medical Sciences, Department of Medicine and HeartOtago, University of Otago, Dunedin, New Zealand.
Cardiovasc Diabetol. 2018 Jun 14;17(1):89. doi: 10.1186/s12933-018-0732-x.
Calcium/calmodulin-dependent kinase II-delta (CaMKIIδ) activity is enhanced during hyperglycemia and has been shown to alter intracellular calcium handling in cardiomyocytes, ultimately leading to reduced cardiac performance. However, the effects of CaMKIIδ on cardiac contractility during type 2 diabetes are undefined.
We examined the expression and activation of CaMKIIδ in right atrial appendages from non-diabetic and type 2 diabetic patients (n = 7 patients per group) with preserved ejection fraction, and also in right ventricular tissue from Zucker Diabetic Fatty rats (ZDF) (n = 5-10 animals per group) during early diabetic cardiac dysfunction, using immunoblot. We also measured whole heart function of ZDF and control rats using echocardiography. Then we measured contraction and relaxation parameters of isolated trabeculae from ZDF to control rats in the presence and absence of CaMKII inhibitors.
CaMKIIδ phosphorylation (at Thr287) was increased in both the diabetic human and animal tissue, indicating increased CaMKIIδ activation in the type 2 diabetic heart. Basal cardiac contractility and relaxation were impaired in the cardiac muscles from the diabetic rats, and CaMKII inhibition with KN93 partially restored contractility and relaxation. Autocamtide-2-related-inhibitor peptide (AIP), another CaMKII inhibitor that acts via a different mechanism than KN93, fully restored cardiac contractility and relaxation.
Our results indicate that CaMKIIδ plays a key role in modulating performance of the diabetic heart, and moreover, suggest a potential therapeutic role for CaMKII inhibitors in improving myocardial function during type 2 diabetes.
钙/钙调蛋白依赖性激酶 II-δ(CaMKIIδ)活性在高血糖期间增强,并已显示改变心肌细胞内的钙处理,最终导致心脏功能降低。然而,CaMKIIδ 在 2 型糖尿病期间对心脏收缩性的影响尚未确定。
我们使用免疫印迹法检查了射血分数保留的非糖尿病和 2 型糖尿病患者(每组 7 例患者)的右心耳和 Zucker 糖尿病肥胖大鼠(ZDF)(每组 5-10 只动物)的右心室组织中 CaMKIIδ 的表达和激活情况。我们还使用超声心动图测量了 ZDF 和对照大鼠的整体心脏功能。然后,我们在存在和不存在 CaMKII 抑制剂的情况下测量了来自 ZDF 到对照大鼠的分离小梁的收缩和松弛参数。
糖尿病患者和动物组织中的 CaMKIIδ 磷酸化(在 Thr287 处)增加,表明 2 型糖尿病心脏中的 CaMKIIδ 激活增加。来自糖尿病大鼠的心肌的基础心脏收缩性和松弛性受损,而 KN93 抑制 CaMKII 部分恢复了收缩性和松弛性。另一种 CaMKII 抑制剂 Autocamtide-2-related-inhibitor peptide(AIP),其作用机制与 KN93 不同,完全恢复了心脏的收缩性和松弛性。
我们的结果表明 CaMKIIδ 在调节糖尿病心脏的功能方面发挥着关键作用,而且,CaMKII 抑制剂在改善 2 型糖尿病期间心肌功能方面具有潜在的治疗作用。