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Updated: Sep 14, 2025

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Herbal Munziq Ameliorates Myocardial Ischemia-Reperfusion Injury by Inhibiting Inflammation
Published on: January 10, 2025
547
Theogallin Protects Myocardial Ischemia-Reperfusion Injury by Inhibiting the Interleukin-17 Signaling Pathway
Feng Zhu1, Huijun Cheng1,2, Zixian Luo1
1National Key Laboratory for Tea Plant Germplasm Innovation and Resource Utilization, School of Tea Science, Anhui Agricultural University, Hefei, Anhui 230036, P.R. China.
Journal of Agricultural and Food Chemistry
|July 21, 2025
Summary
Theogallin, a tea polyphenol, protects against heart damage from ischemia-reperfusion (I/R) injury. It reduces infarct size and improves heart function by downregulating the interleukin-17 (IL-17) signaling pathway.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Molecular Biology
Background:
- Tea polyphenols exhibit cardioprotective effects via antioxidant and anti-inflammatory actions.
- Theogallin, a unique tea-derived polyphenol, has an unclear role in preventing myocardial ischemia-reperfusion (I/R) injury.
- Understanding theogallin's mechanism is crucial for developing novel therapeutic strategies for heart conditions.
Purpose of the Study:
- To investigate the cardioprotective effects of theogallin against myocardial I/R injury.
- To elucidate the underlying molecular mechanisms, particularly the involvement of the IL-17 signaling pathway.
- To evaluate theogallin's efficacy in both ex vivo and in vivo models of cardiac injury.
Main Methods:
- Utilized an ex vivo Langendorff perfusion model of I/R injury in isolated rat hearts.
- Employed an in vivo myocardial injury model using left anterior descending coronary artery (LAD) ligation in rats.
- Assessed hemodynamic parameters, myocardial enzyme release, infarct size, fibrosis, and gene expression related to the IL-17 pathway.
Main Results:
- Theogallin pretreatment significantly improved hemodynamic function in isolated hearts subjected to I/R.
- In vivo, theogallin administration enhanced myocardial contractile function and reduced cardiac enzyme release.
- Theogallin significantly decreased infarct size and cardiac fibrosis, while downregulating key IL-17 pathway components (IL-17RA, JUNB, FRA1, MMP9).
Conclusions:
- Theogallin demonstrates significant cardioprotective effects against myocardial I/R injury in rat models.
- These protective effects are mediated by the inhibition of the IL-17 signaling pathway.
- Theogallin represents a potential therapeutic agent for managing myocardial I/R injury.
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