Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway

Author:

Peng Meizhong1ORCID,Liu Hanying1ORCID,Ji Qingxuan1ORCID,Ma Pan1ORCID,Niu Yiting1ORCID,Ning Shangqiu2ORCID,Sun Huihui1ORCID,Pang Xinxin3ORCID,Yang Yuqian3ORCID,Zhang Yuting4ORCID,Han Jing4ORCID,Hao Gaimei56ORCID

Affiliation:

1. College of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China

2. Beijing Anzhen Hospital, Capital Medical University, Beijing, China

3. School of Chinese Material Medica, Beijing University of Chinese Medicine, Beijing, China

4. Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China

5. Institute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China

6. Gansu Provincial Hospital of Traditional Chinese Medicine, Gansu, China

Abstract

Diabetic cardiomyopathy (DCM) is one of the main complications of diabetic patients and the major reason for the high prevalence of heart failure in diabetic patients. Fufang Xueshuantong (FXST) is a traditional Chinese medicine formula commonly used in the treatment of diabetic retinopathy and stable angina pectoris. However, the role of FXST in DCM has not yet been clarified. This study was conducted to investigate the effects of FXST on diabetic myocardial lesions and reveal its molecular mechanism. The rats were intraperitoneally injected with 65 mg/kg streptozotocin (STZ) to induce diabetes mellitus (DM). DM rats were given saline or FXST. The rats in the control group were intraperitoneally injected with an equal amount of sodium citrate buffer and gavaged with saline. After 12 weeks, echocardiography, heart weight index (HWI), and myocardial pathological changes were determined. The expression of transforming growth factor-beta1 (TGF-β1), collagen I, and collagen III was examined using immunofluorescence staining and western blot. The expressions of Wnt/β-catenin signaling pathway-related proteins and mRNA were detected by western blot and real-time PCR. The results showed that FXST significantly improved cardiac function, ameliorated histopathological changes, and decreased HWI in the DM rats. FXST significantly inhibited the expression of myocardial TGF-β1, collagen I, and collagen III in DM rats. Furthermore, FXST significantly inhibited the Wnt/β-catenin pathway. Taken together, FXST has a protective effect on DCM, which might be mediated by suppressing the Wnt/β-catenin pathway.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Endocrine and Autonomic Systems,Endocrinology,Endocrinology, Diabetes and Metabolism

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