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.
Abstract

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