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Resistant starch confers protection of dietary against diabetic cardiomyopathy
Qingqing Zhu1, Xinyi Lu1, Ting Zhang1
1State Key Laboratory for Innovation and Transformation of Luobing Theory. Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Abstract:
Long-term dysfunction of glucose metabolism causes cardiac dysfunction called diabetic cardiomyopathy (DCM). To investigate the effect and underlying mechanism of RS on the process of DCM, mouse models induced by a high-fat diet (HFD) and streptozotocin (STZ) were fed RS (2 g/kg/day) and vehicle treatment (by oral gavage) for 14 weeks. Various analyses, including qRT-PCR, western blot, immunofluorescence staining, histology staining, cardiac function, and diversity detection of intestinal microbiota were performed. RS intervention could directly improve myocardial fibrosis, hypertrophy, apoptosis, and cardiac insufficiency in DCM. These beneficial effects may be achieved by elevating the expression of IGF-1, activating the ERK phosphorylation. Furthermore, by carrying out nano LC-MS/MS analyses and 16S rDNA sequencing, we found RS might primarily affect proteins in the cytoplasm involved in post-translational modification, protein conversion, and signal transduction mechanisms. RS altered intestinal microbiota and improved intestinal mucosal permeability towards a favorable direction in DCM. This multidimensional assessment of RS suggests that might be a promising approach towards the treatment of DCM.
Insights
Resistant starch (RS) improves cardiac function in diabetic cardiomyopathy (DCM) by reducing fibrosis and apoptosis. RS also positively impacts gut microbiota and protein pathways, offering a potential treatment for DCM.
Area of Science:
- Cardiology
- Metabolic Disorders
- Microbiology
Background:
- Diabetic cardiomyopathy (DCM) results from long-term glucose metabolism dysfunction.
- Understanding mechanisms to treat DCM is crucial.
Purpose of the Study:
- To investigate the effects of resistant starch (RS) on DCM.
- To elucidate the underlying mechanisms of RS in treating DCM.
Main Methods:
- Mouse models of DCM induced by high-fat diet (HFD) and streptozotocin (STZ).
- Intervention with RS (2 g/kg/day) or vehicle for 14 weeks.
- Analyses included qRT-PCR, Western blot, immunofluorescence, histology, cardiac function tests, intestinal microbiota sequencing, and nano LC-MS/MS.
Main Results:
- RS improved myocardial fibrosis, hypertrophy, apoptosis, and cardiac insufficiency in DCM mice.
- RS increased IGF-1 expression and ERK phosphorylation.
- RS modulated intestinal microbiota composition and enhanced intestinal barrier function.
Conclusions:
- Resistant starch (RS) demonstrates therapeutic potential for diabetic cardiomyopathy (DCM).
- RS acts through improving cardiac parameters, modulating protein expression and signaling pathways, and beneficially altering the gut microbiome.
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