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尼可地尔可预防 Gαq 诱导的转基因小鼠进行性心力衰竭和室性心律失常。

Nicorandil prevents Gαq-induced progressive heart failure and ventricular arrhythmias in transgenic mice.

机构信息

Department of Molecular and Cellular Pharmacology, Iwate Medical University School of Pharmaceutical Sciences, Shiwa, Iwate, Japan.

出版信息

PLoS One. 2012;7(12):e52667. doi: 10.1371/journal.pone.0052667. Epub 2012 Dec 20.

Abstract

BACKGROUND

Beneficial effects of nicorandil on the treatment of hypertensive heart failure (HF) and ischemic heart disease have been suggested. However, whether nicorandil has inhibitory effects on HF and ventricular arrhythmias caused by the activation of G protein alpha q (Gα(q)) -coupled receptor (GPCR) signaling still remains unknown. We investigated these inhibitory effects of nicorandil in transgenic mice with transient cardiac expression of activated Gα(q) (Gα(q)-TG).

METHODOLOGY/PRINCIPAL FINDINGS: Nicorandil (6 mg/kg/day) or vehicle was chronically administered to Gα(q)-TG from 8 to 32 weeks of age, and all experiments were performed in mice at the age of 32 weeks. Chronic nicorandil administration prevented the severe reduction of left ventricular fractional shortening and inhibited ventricular interstitial fibrosis in Gα(q)-TG. SUR-2B and SERCA2 gene expression was decreased in vehicle-treated Gα(q)-TG but not in nicorandil-treated Gα(q)-TG. eNOS gene expression was also increased in nicorandil-treated Gα(q)-TG compared with vehicle-treated Gα(q)-TG. Electrocardiogram demonstrated that premature ventricular contraction (PVC) was frequently (more than 20 beats/min) observed in 7 of 10 vehicle-treated Gα(q)-TG but in none of 10 nicorandil-treated Gα(q)-TG. The QT interval was significantly shorter in nicorandil-treated Gα(q)-TG than vehicle-treated Gα(q)-TG. Acute nicorandil administration shortened ventricular monophasic action potential duration and reduced the number of PVCs in Langendorff-perfused Gα(q)-TG mouse hearts. Moreover, HMR1098, a blocker of cardiac sarcolemmal K(ATP) channels, significantly attenuated the shortening of MAP duration induced by nicorandil in the Gα(q)-TG heart.

CONCLUSIONS/SIGNIFICANCE: These findings suggest that nicorandil can prevent the development of HF and ventricular arrhythmia caused by the activation of GPCR signaling through the shortening of the QT interval, action potential duration, the normalization of SERCA2 gene expression. Nicorandil may also improve the impaired coronary circulation during HF.

摘要

背景

尼可地尔对高血压性心力衰竭(HF)和缺血性心脏病的治疗有益处已被证实。然而,尼可地尔是否对 G 蛋白α q(Gα(q))-偶联受体(GPCR)信号激活引起的 HF 和心室性心律失常有抑制作用仍不清楚。我们在瞬时心脏表达激活的 Gα(q)(Gα(q)-TG)的转基因小鼠中研究了尼可地尔的这些抑制作用。

方法/主要发现:尼可地尔(6mg/kg/天)或载体从 8 到 32 周龄持续给予 Gα(q)-TG,所有实验均在 32 周龄的小鼠中进行。慢性尼可地尔给药可防止左心室缩短分数的严重降低,并抑制 Gα(q)-TG 的心室间质纤维化。在载体处理的 Gα(q)-TG 中,SUR-2B 和 SERCA2 基因表达减少,但在尼可地尔处理的 Gα(q)-TG 中没有减少。与载体处理的 Gα(q)-TG 相比,尼可地尔处理的 Gα(q)-TG 中 eNOS 基因表达也增加。心电图显示,在 10 只载体处理的 Gα(q)-TG 中,7 只(每分钟超过 20 次)经常出现室性早搏(PVC),而在 10 只尼可地尔处理的 Gα(q)-TG 中均未出现。尼可地尔处理的 Gα(q)-TG 的 QT 间期明显短于载体处理的 Gα(q)-TG。急性尼可地尔给药缩短了 Langendorff 灌注的 Gα(q)-TG 小鼠心脏的心室单相动作电位持续时间,并减少了 PVC 的数量。此外,心脏肌浆网 K(ATP)通道阻滞剂 HMR1098 显著减弱了尼可地尔在 Gα(q)-TG 心脏中引起的 MAP 持续时间缩短。

结论/意义:这些发现表明,尼可地尔通过缩短 QT 间期、动作电位持续时间、SERCA2 基因表达的正常化,可预防 GPCR 信号激活引起的 HF 和室性心律失常的发生。尼可地尔还可能改善 HF 期间受损的冠状动脉循环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59a1/3527603/b049c65ef342/pone.0052667.g001.jpg

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