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β-elemene alleviates hyperglycemia-induced cardiac inflammation and remodeling by inhibiting the JAK/STAT3-NF-κB
Jiong Wang1, Chenchen Qian2, Yue Chen3
1Joint Research Centre on Medicine, the Affiliated Xiangshan Hospital of Wenzhou Medical University, Ningbo, Zhejiang 315700, China; Chemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Insights
β-elemene (Ele) effectively treats diabetic cardiomyopathy by reducing cardiac inflammation and hypertrophy. This natural compound preserves heart function in diabetic mice by inhibiting key inflammatory pathways.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Diabetology
Background:
- Diabetic cardiomyopathy involves cardiac hypertrophy and inflammation.
- β-elemene (Ele), a natural compound, has anti-inflammatory properties.
- The efficacy of Ele in diabetic cardiomyopathy is not well-established.
Purpose of the Study:
- To evaluate the therapeutic effect of Ele on hyperglycemia-induced cardiac remodeling and heart failure.
- To investigate the underlying mechanisms of Ele's action in diabetic cardiomyopathy.
Main Methods:
- Diabetic cardiomyopathy (DCM) induced in C57BL/6 mice using streptozotocin.
- Oral administration of Ele for 8 weeks post-induction.
- Cardiac tissue RNA sequencing to elucidate mechanisms.
Main Results:
- Ele significantly reduced cardiac inflammation, fibrosis, and hypertrophy in diabetic mice and high glucose-treated cardiomyocytes.
- RNA sequencing revealed the JAK/STAT3-NF-κB signaling pathway mediates Ele's cardioprotective effects.
- Ele inhibited JAK2 and STAT3 phosphorylation and NF-κB activation, alleviating inflammation.
Conclusions:
- Ele preserves heart function in diabetic mice by inhibiting inflammatory responses.
- The JAK/STAT3 and NF-κB pathways are key targets of Ele's action.
- Ele shows promise as an effective therapy for diabetic cardiomyopathy.
Background:
Hyperglycemic induced cardiac hypertrophy and cardiac inflammation are important pathological processes in diabetic cardiomyopathy. β-elemene (Ele) is a natural compound extracted from Curcuma Rhizoma and has anti-tumor effects. It also has therapeutic effects in some inflammatory diseases. However, the therapeutic effect of Ele on diabetic cardiomyopathy is not clear. The purpose of this study was to evaluate the effect of Ele on hyperglycemia-caused cardiac remodeling and heart failure.
Methods:
C57BL/6 mice were intraperitoneally injected with streptozotocin to induce DCM, and Ele was administered intragastric after 8 weeks to investigate the effect of Ele. RNA sequencing of cardiac tissue was performed to investigate the mechanism.
Results:
Ele markedly inhibited cardiac inflammation, fibrosis and hypertrophy in diabetic mice, as well as in high glucose-induced cardiomyocytes. RNA sequencing showed that cardioprotective effect of Ele involved the JAK/STAT3-NF-κB signaling pathway. Ele alleviated heart and cardiomyocyte inflammation in mice by blocking diabetes-induced JAK2 and STAT3 phosphorylation and NF-κB activation.
Conclusions:
The study found that Ele preserved the hearts of diabetic mice by inhibiting JAK/STAT3 and NF-κB mediated inflammatory responses, suggesting that Ele is an effective therapy for DCM.
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