» Articles » PMID: 37261285

Effect of Tanshinone IIA for Myocardial Ischemia/reperfusion Injury in Animal Model: Preclinical Evidence and Possible Mechanisms

Overview
Journal Front Pharmacol
Date 2023 Jun 1
PMID 37261285
Authors
Affiliations
Soon will be listed here.
Abstract

Tanshinone IIA (Tan IIA), the major active lipophilic ingredient of , exerts various therapeutic effects on the cardiovascular system. We aimed to identify the preclinical evidence and possible mechanisms of Tan IIA as a cardioprotective agent in the treatment of myocardial ischemia/reperfusion injury. The study quality scores of twenty-eight eligible studies and data analyses were separately assessed using the CAMARADES 10-item checklist and Rev-Man 5.3 software. The study quality score ranged from 3/10 to 7/10 points. The present study provided preliminary preclinical evidence that Tan IIA could significantly decrease the myocardial infarct size, cardiac enzyme activity and troponin levels compared with those in the control group (). Tan IIA alleviated myocardial I/R injury via antioxidant, anti-inflammatory, anti-apoptosis mechanisms and improved circulation and energy metabolism. Thus, Tan IIA is a promising cardioprotective agent for the treatment of myocardial ischemia/reperfusion injury and should be further investigated in clinical trials.

Citing Articles

Chinese and western medicine treatment of myocardial fibrosis drugs.

Zhu Y, Zhang F, Li Z, Zhou Y, Shu Y, Ruan J Front Cardiovasc Med. 2025; 11:1477601.

PMID: 39882321 PMC: 11774883. DOI: 10.3389/fcvm.2024.1477601.


Tanshinone IIA Protects Ischemia/Reperfusion-Induced Cardiomyocyte Injury by Inhibiting the / Axis.

Wang Y, Sun W, Shen L, Yu P, Shen Q, Zhou Y Cardiol Res Pract. 2024; 2024:2581638.

PMID: 39568660 PMC: 11578662. DOI: 10.1155/2024/2581638.


Recent advances of traditional Chinese medicine against cardiovascular disease: overview and potential mechanisms.

Dai J, Qiu L, Lu Y, Li M Front Endocrinol (Lausanne). 2024; 15:1366285.

PMID: 39403576 PMC: 11471557. DOI: 10.3389/fendo.2024.1366285.


Inflammation and coronary microvascular disease: relationship, mechanism and treatment.

Guo Z, Yang Z, Song Z, Li Z, Xiao Y, Zhang Y Front Cardiovasc Med. 2024; 11:1280734.

PMID: 38836066 PMC: 11148780. DOI: 10.3389/fcvm.2024.1280734.


Expanding the therapeutic potential of : a review of its pharmacological applications in musculoskeletal diseases.

Ye Z, Liu Y, Song J, Gao Y, Fang H, Hu Z Front Pharmacol. 2023; 14:1276038.

PMID: 38116081 PMC: 10728493. DOI: 10.3389/fphar.2023.1276038.


References
1.
Lecour S, Botker H, Condorelli G, Davidson S, Garcia-Dorado D, Engel F . ESC working group cellular biology of the heart: position paper: improving the preclinical assessment of novel cardioprotective therapies. Cardiovasc Res. 2014; 104(3):399-411. PMC: 4242141. DOI: 10.1093/cvr/cvu225. View

2.
Macleod M, OCollins T, Howells D, Donnan G . Pooling of animal experimental data reveals influence of study design and publication bias. Stroke. 2004; 35(5):1203-8. DOI: 10.1161/01.STR.0000125719.25853.20. View

3.
Thind G, Agrawal P, Hirsh B, Saravolatz L, Chen-Scarabelli C, Narula J . Mechanisms of myocardial ischemia-reperfusion injury and the cytoprotective role of minocycline: scope and limitations. Future Cardiol. 2015; 11(1):61-76. DOI: 10.2217/fca.14.76. View

4.
Landis S, Amara S, Asadullah K, Austin C, Blumenstein R, Bradley E . A call for transparent reporting to optimize the predictive value of preclinical research. Nature. 2012; 490(7419):187-91. PMC: 3511845. DOI: 10.1038/nature11556. View

5.
Ferdinandy P, Hausenloy D, Heusch G, Baxter G, Schulz R . Interaction of risk factors, comorbidities, and comedications with ischemia/reperfusion injury and cardioprotection by preconditioning, postconditioning, and remote conditioning. Pharmacol Rev. 2014; 66(4):1142-74. DOI: 10.1124/pr.113.008300. View