Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats
Abstract Skimmin, a natural coumarin derivate, has been showed to be protective against experimental diabetic nephropathy; however, its protective effect on diabetic cardiomyopathy (DCM) is not clarified. By using in vitro and in vivo models, we investigated skimmin's protective effect on impai...
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Online Access: | https://doi.org/10.1002/kjm2.12305 |
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doaj-6993b8e412134b3f9fb5182d11ac57f82021-02-12T05:04:32ZengWileyKaohsiung Journal of Medical Sciences1607-551X2410-86502021-02-0137213614410.1002/kjm2.12305Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic ratsRui‐Kai Liang0Yun‐Yun Zhao1Mei‐Li Shi2Gang Zhang3Yong‐Jun Zhao4Bing‐Gui Zhang5Rui‐Jing Liang6Department of Endocrinology Hebei Geriatric Hospital Shijiazhuang Hebei ChinaDepartment of Cardiovascular Medicine Hebei Geriatric Hospital Shijiazhuang Hebei ChinaDepartment of Cardiovascular Medicine Hebei Geriatric Hospital Shijiazhuang Hebei ChinaDepartment of Cardiovascular Medicine Hebei Geriatric Hospital Shijiazhuang Hebei ChinaDepartment of Cardiovascular Medicine Hebei Geriatric Hospital Shijiazhuang Hebei ChinaDepartment of General Surgery Hebei Geriatric Hospital Shijiazhuang Hebei ChinaDepartment of Geriatrics The First Hospital of Hebei Medical University Shijiazhuang Hebei ChinaAbstract Skimmin, a natural coumarin derivate, has been showed to be protective against experimental diabetic nephropathy; however, its protective effect on diabetic cardiomyopathy (DCM) is not clarified. By using in vitro and in vivo models, we investigated skimmin's protective effect on impaired heart tissues in DCM. DCM was induced by streptozotocin (STZ, 60 mg/kg) using Sprague Dawley rats, and diabetic rats were treated with either skimmin (15 or 30 mg/kg) or the vehicle for 16 weeks, and normal rats were used as a control. Hematoxylin and eosin and Masson's trichrome staining were performed to evaluate the cardiac histopathology, and the oxidative stress and proinflammation cytokines in heart tissues were measured. The protein levels of key mediators in fibrosis, pyroptosis, and autophagy in heart tissues were investigated using western blotting. In vitro, primary neonatal cardiomyocytes were treated with skimmin (2 and 10 μM) under stimulation by high glucose (30 mM) and low glucose (5 mM) respectively, and the molecular mechanisms on pyroptosis and autophagy were studied. Compared to the vehicle‐treated DCM group, skimmin treatment significantly improved the ejection fraction and fractional shortening of the left ventricle and reduced the oxidative stress by increasing the glutathione level and activity of superoxide dismutase and catalase. Skimmin also reduced cardiac fibrosis, and decreased proinflammation cytokines in cardiac tissues. Mechanism studies showed skimmin may enhance the autophagy and ameliorate NLRP3 inflammasome activation to play a protective role in DCM. This study, for the first time, indicates that skimmin might be a promising lead compound for DCM.https://doi.org/10.1002/kjm2.12305autophagydiabetic cardiomyopathyinflammationoxidative stressskimmin |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rui‐Kai Liang Yun‐Yun Zhao Mei‐Li Shi Gang Zhang Yong‐Jun Zhao Bing‐Gui Zhang Rui‐Jing Liang |
spellingShingle |
Rui‐Kai Liang Yun‐Yun Zhao Mei‐Li Shi Gang Zhang Yong‐Jun Zhao Bing‐Gui Zhang Rui‐Jing Liang Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats Kaohsiung Journal of Medical Sciences autophagy diabetic cardiomyopathy inflammation oxidative stress skimmin |
author_facet |
Rui‐Kai Liang Yun‐Yun Zhao Mei‐Li Shi Gang Zhang Yong‐Jun Zhao Bing‐Gui Zhang Rui‐Jing Liang |
author_sort |
Rui‐Kai Liang |
title |
Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats |
title_short |
Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats |
title_full |
Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats |
title_fullStr |
Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats |
title_full_unstemmed |
Skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats |
title_sort |
skimmin protects diabetic cardiomyopathy in streptozotocin‐induced diabetic rats |
publisher |
Wiley |
series |
Kaohsiung Journal of Medical Sciences |
issn |
1607-551X 2410-8650 |
publishDate |
2021-02-01 |
description |
Abstract Skimmin, a natural coumarin derivate, has been showed to be protective against experimental diabetic nephropathy; however, its protective effect on diabetic cardiomyopathy (DCM) is not clarified. By using in vitro and in vivo models, we investigated skimmin's protective effect on impaired heart tissues in DCM. DCM was induced by streptozotocin (STZ, 60 mg/kg) using Sprague Dawley rats, and diabetic rats were treated with either skimmin (15 or 30 mg/kg) or the vehicle for 16 weeks, and normal rats were used as a control. Hematoxylin and eosin and Masson's trichrome staining were performed to evaluate the cardiac histopathology, and the oxidative stress and proinflammation cytokines in heart tissues were measured. The protein levels of key mediators in fibrosis, pyroptosis, and autophagy in heart tissues were investigated using western blotting. In vitro, primary neonatal cardiomyocytes were treated with skimmin (2 and 10 μM) under stimulation by high glucose (30 mM) and low glucose (5 mM) respectively, and the molecular mechanisms on pyroptosis and autophagy were studied. Compared to the vehicle‐treated DCM group, skimmin treatment significantly improved the ejection fraction and fractional shortening of the left ventricle and reduced the oxidative stress by increasing the glutathione level and activity of superoxide dismutase and catalase. Skimmin also reduced cardiac fibrosis, and decreased proinflammation cytokines in cardiac tissues. Mechanism studies showed skimmin may enhance the autophagy and ameliorate NLRP3 inflammasome activation to play a protective role in DCM. This study, for the first time, indicates that skimmin might be a promising lead compound for DCM. |
topic |
autophagy diabetic cardiomyopathy inflammation oxidative stress skimmin |
url |
https://doi.org/10.1002/kjm2.12305 |
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