LongShengZhi capsule inhibits doxorubicin-induced heart failure by anti-oxidative stress

Shuai Xu1, Yuanyu Wang1, Maoyun Yu2

  • 1Key Laboratory of Metabolism and Regulation for Major Diseases of Anhui Higher Education Institutes, College of Food and Biological Engineering, Hefei University of Technology, Hefei, China.

Insights

LongShengZhi capsule (LSZ) effectively treats doxorubicin-induced heart failure in mice. LSZ reduces cardiac fibrosis, inflammation, and apoptosis, offering a potential therapeutic for heart failure.

Area of Science:

  • Cardiology
  • Pharmacology
  • Traditional Chinese Medicine

Background:

  • Heart failure is a significant global health burden.
  • Doxorubicin (DOX) is a chemotherapy agent known to induce cardiotoxicity.
  • Traditional Chinese Medicine (TCM) offers potential therapeutic avenues for cardiovascular diseases.

Purpose of the Study:

  • To investigate the cardioprotective effects of LongShengZhi capsule (LSZ) against doxorubicin (DOX)-induced heart failure in a mouse model.
  • To elucidate the underlying mechanisms of LSZ's therapeutic action.

Main Methods:

  • C57BL/6 mice were divided into control, DOX-induced heart failure, and DOX + LSZ treatment groups.
  • DOX was administered to induce heart failure, while LSZ was given orally with chow.
  • Cardiac function markers, fibrosis, apoptosis, inflammation, oxidative stress, and relevant gene/protein expressions were assessed.

Main Results:

  • LSZ treatment significantly ameliorated DOX-induced increases in serum cardiac enzymes and cardiac fibrosis.
  • LSZ inhibited DOX-induced apoptosis by reducing caspase 3 activity and expression.
  • LSZ decreased inflammatory cytokine levels and reduced oxidative stress by upregulating antioxidant enzymes (SOD1, SOD2, catalase, GPx1) via FOXO3A and SIRT3 activation.

Conclusions:

  • LSZ demonstrates significant cardioprotective effects against DOX-induced heart failure in mice.
  • LSZ mitigates heart failure by reducing oxidative stress, inflammation, and apoptosis.
  • LSZ holds promise as a potential therapeutic agent for heart failure management.

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