Mechanisms of Chinese Medicine Xinmailong’s protection against heart failure in pressure-overloaded mice and cultured cardiomyocytes

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作者
Jianyong Qi
Juan Yu
Yafang Tan
Renshan Chen
Wen Xu
Yanfen Chen
Jun Lu
Qin Liu
Jiashin Wu
Weiwang Gu
Minzhou Zhang
机构
[1] AMI Key Laboratory of Chinese Medicine,Department of Pharmaceutical Sciences
[2] Guangdong Province Academy of Chinese Medicine,undefined
[3] Guangdong Province Hospital of Chinese Medicine,undefined
[4] 2nd Affiliated Hospital of Guangzhou University of Chinese Medicine,undefined
[5] Animal Laboratory,undefined
[6] Southern Medical University,undefined
[7] Animal Laboratory,undefined
[8] 2nd Affiliated Hospital of Guangzhou University of Chinese Medicine,undefined
[9] Lab of Chinese Materia Medica Preparation,undefined
[10] 2nd Affiliated Hospital of Guangzhou University of Chinese Medicine,undefined
[11] Puning Hospital of Chinese Medicine,undefined
[12] College of Pharmacy,undefined
[13] Northeast Ohio Medical University,undefined
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摘要
Patients with heart failure (HF) have high mortality and mobility. Xinmailong (XML) injection, a Chinese Medicine, is clinically effective in treating HF. However, the mechanism of XML’s effectiveness on HF was unclear, and thus, was the target of the present study. We created a mouse model of pressure-overload-induced HF with transverse aortic constriction (TAC) surgery and compared among 4 study groups: SHAM (n = 10), TAC (n = 12), MET (metoprolol, positive drug treatment, n = 7) and XML (XML treatment, n = 14). Dynamic changes in cardiac structure and function were evaluated with echocardiography in vivo. In addition, H9C2 rat cardiomyocytes were cultured in vitro and the phosphorylation of ERK1/2, AKT, GSK3β and protein expression of GATA4 in nucleus were detected with Western blot experiment. The results showed that XML reduced diastolic thickness of left ventricular posterior wall, increased ejection fraction and fraction shortening, so as to inhibit HF at 2 weeks after TAC. Moreover, XML inhibited the phosphorylation of ERK1/2, AKT and GSK3β, subsequently inhibiting protein expression of GATA4 in nucleus (P < 0.001). Together, our data demonstrated that XML inhibited the TAC-induced HF via inactivating the ERK1/2, AKT/GSK3β, and GATA4 signaling pathway.
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