Why the study?
Does Guanmaitong reduce myocardial infarction size and improve apoptosis and inflammation in a rat model of acute myocardial infarction?
Does Guanmaitong reduce myocardial infarction size and improve apoptosis and inflammation in a rat model of acute myocardial infarction?
Guanmaitong exerts cardioprotective effects in a rat model of acute myocardial infarction by reducing infarct size and inhibiting apoptosis and inflammation.
Hypothesis-generating for Guanmaitong in rat AMI; human trials needed before any clinical consideration.
Guanmaitong (GMT) is a traditional Chinese herbal compound that has been used for the treatment of coronary heart disease (CHD) and other cardiovascular diseases. However, the efficacy of GMT in treating cardiovascular diseases remains unclear. The aim of the present study was to investigate the protective mechanisms and identify the targeted proteins and signaling networks associated with the physiological activity of GMT in a rat model of acute myocardial infarction (AMI). Sprague-Dawley rats were randomly allocated into five groups: Control group (sham-operated), the model group, and small, medium, and large dosage GMT groups. The rat model of AMI was established via ligation of the coronary artery. The results indicate that GMT was able to reduce myocardial infarction size and improve the activities of tumor necrosis factor-α (TNF-α), intercellular adhesion molecule 1 (ICAM-1) and interleukin-1. Furthermore, the reduced apoptotic index of the GMT-treated cardiocytes (P<0.05 vs. model group) was in accordance with the downregulated expression of Bax and the upregulated expression of Bcl-2. In conclusion, GMT may exert a protective potential against myocardial infarction injury by inhibiting apoptosis and inflammation of cardiomyocytes, and may offer a promising adjunct treatment for CHD.
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Wang et al. (2016) studied this question.
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