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

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 stab...

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Autores principales: Peng, Meizhong, Liu, Hanying, Ji, Qingxuan, Ma, Pan, Niu, Yiting, Ning, Shangqiu, Sun, Huihui, Pang, Xinxin, Yang, Yuqian, Zhang, Yuting, Han, Jing, Hao, Gaimei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553353/
https://www.ncbi.nlm.nih.gov/pubmed/36237833
http://dx.doi.org/10.1155/2022/3919161
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author Peng, Meizhong
Liu, Hanying
Ji, Qingxuan
Ma, Pan
Niu, Yiting
Ning, Shangqiu
Sun, Huihui
Pang, Xinxin
Yang, Yuqian
Zhang, Yuting
Han, Jing
Hao, Gaimei
author_facet Peng, Meizhong
Liu, Hanying
Ji, Qingxuan
Ma, Pan
Niu, Yiting
Ning, Shangqiu
Sun, Huihui
Pang, Xinxin
Yang, Yuqian
Zhang, Yuting
Han, Jing
Hao, Gaimei
author_sort Peng, Meizhong
collection PubMed
description 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.
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spelling pubmed-95533532022-10-12 Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway Peng, Meizhong Liu, Hanying Ji, Qingxuan Ma, Pan Niu, Yiting Ning, Shangqiu Sun, Huihui Pang, Xinxin Yang, Yuqian Zhang, Yuting Han, Jing Hao, Gaimei Int J Endocrinol Research Article 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. Hindawi 2022-09-19 /pmc/articles/PMC9553353/ /pubmed/36237833 http://dx.doi.org/10.1155/2022/3919161 Text en Copyright © 2022 Meizhong Peng et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Peng, Meizhong
Liu, Hanying
Ji, Qingxuan
Ma, Pan
Niu, Yiting
Ning, Shangqiu
Sun, Huihui
Pang, Xinxin
Yang, Yuqian
Zhang, Yuting
Han, Jing
Hao, Gaimei
Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway
title Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway
title_full Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway
title_fullStr Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway
title_full_unstemmed Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway
title_short Fufang Xueshuantong Improves Diabetic Cardiomyopathy by Regulating the Wnt/β-Catenin Pathway
title_sort fufang xueshuantong improves diabetic cardiomyopathy by regulating the wnt/β-catenin pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553353/
https://www.ncbi.nlm.nih.gov/pubmed/36237833
http://dx.doi.org/10.1155/2022/3919161
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