Tianjin Key Laboratory of Ionic‑Molecular Function of Cardiovascular Disease, Department of Cardiology, Tianjin Institute of Cardiology, Second Hospital of Tianjin Medical University, Tianjin 300211, P.R. China.
Mol Med Rep. 2018 Apr;17(4):4933-4940. doi: 10.3892/mmr.2018.8472. Epub 2018 Jan 24.
Diabetes is an independent risk factor for atrial fibrillation (AF); however, the underlying mechanism linking diabetes and AF remains to be clarified. The present study aimed to explore the molecular mechanism of increased reactive oxygen species (ROS) production in AF and the ROS‑mediated downstream events in diabetes. Firstly, the atrial fibroblasts were isolated from the left atrium of rabbits using enzyme digestion and differential adhesion. Then, the isolated cells were identified by morphology analysis under a microscope, collagen distribution using Masson trichrome staining and vimentin by immunofluorescence. Following this, the collected atrial fibroblasts were randomly divided into 7 groups and administered with high glucose (25 mM glucose), H2O2 stimulation (100 nmol/l), glucose + apocynin (100 µg/ml), H2O2 + apocynin, glucose + H2O2, and a combination of glucose, apocynin and H2O2, as well as the negative control (NC). An MTS assay was performed to investigate cell proliferation following the different treatments, and western blotting was conducted to explore the expression of several proteins including NAD(P)H oxidative (NOX) subunits, key factors involved in mitogen‑activated protein kinase (MAPK) signaling pathways and matrix metalloproteinases (MMPs). The atrial fibroblasts were spindle‑shaped with one or more protuberances. Vimentin was positively expressed in collected cells under confocal laser scanning microscopy. This result indicated that the atrial fibroblasts were successfully prepared. High glucose and H2O2 stimulation significantly increased the proliferation of atrial fibroblasts and apocynin markedly attenuated the promoting effects on cell proliferation induced by high glucose and H2O2 treatment (P<0.05). Additionally, high glucose and H2O2 stimulation increased the expression of Rac1, phospho(p)‑c‑Jun N‑terminal kinase 1, p38, p‑p38 and MMP9, which was markedly decreased by the addition of apocynin (P<0.05). The mechanism associated with diabetes and AF may be attributed to oxidative stress (ROS production) derived from NOX activity, and then induced activation of the MAPK signaling pathways and MMP9 expression.
糖尿病是心房颤动(AF)的独立危险因素;然而,将糖尿病与 AF 联系起来的潜在机制仍需阐明。本研究旨在探讨 AF 中活性氧(ROS)产生增加的分子机制以及糖尿病中 ROS 介导的下游事件。首先,使用酶消化和差速贴壁法从兔左心房分离心房成纤维细胞。然后,通过显微镜下的形态分析、Masson 三色染色法检测胶原分布和免疫荧光法检测波形蛋白来鉴定分离的细胞。接下来,将收集的心房成纤维细胞随机分为 7 组,并给予高葡萄糖(25 mM 葡萄糖)、H2O2 刺激(100 nmol/L)、葡萄糖+apocynin(100 μg/ml)、H2O2+apocynin、葡萄糖+H2O2 以及葡萄糖、apocynin 和 H2O2 的组合以及阴性对照(NC)处理。进行 MTS 测定以研究不同处理后细胞的增殖情况,并进行 Western blot 分析以研究包括 NAD(P)H 氧化酶(NOX)亚基、丝裂原活化蛋白激酶(MAPK)信号通路和基质金属蛋白酶(MMPs)关键因子在内的几种蛋白的表达。心房成纤维细胞呈梭形,有一个或多个突起。在共聚焦激光扫描显微镜下,收集的细胞中阳性表达波形蛋白。这表明成功制备了心房成纤维细胞。高葡萄糖和 H2O2 刺激显著增加了心房成纤维细胞的增殖,apocynin 明显减弱了高葡萄糖和 H2O2 处理诱导的细胞增殖促进作用(P<0.05)。此外,高葡萄糖和 H2O2 刺激增加了 Rac1、磷酸化(p)-c-Jun N-末端激酶 1(p-JNK1)、p38、p-p38 和 MMP9 的表达,apocynin 的加入显著降低了这些表达(P<0.05)。与糖尿病和 AF 相关的机制可能归因于来自 NOX 活性的氧化应激(ROS 产生),然后诱导 MAPK 信号通路和 MMP9 表达的激活。