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Updated: Feb 8, 2026

Improved Rodent Model of Myocardial Ischemia and Reperfusion Injury
Published on: March 7, 2022
Protective Effects of Shenfu Injection against Myocardial Ischemia-Reperfusion Injury via Activation of eNOS in Rats
Yan-Yan Wang1,2,3, Yan-Yan Li3, Lin Li1,2,3
1Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin University of Traditional Chinese Medicine.
Abstract:
The aim of the present study was to investigate the protective effects of Shenfu injection (SFI) against myocardial ischemia-reperfusion injury (MIRI) in model rats and to explore its mechanism of action. Sprague-Dawley (SD) rats were pretreated with SFI and NG-nitro-L-arginine methyl ester (L-NAME) via tail vein injection and then rats were subjected to ischemia by occlusion of the left anterior descending coronary artery for 30 min followed by reperfusion for 120 min. Left ventricular function was evaluated by echocardiography. Hemodynamic was measured by the Millar pressure-volume system; serum creatine kinase (CK), lactate dehydrogenase (LDH) and serum troponin (TNNI3) levels were determined. Myocardial infarct size was observed by 2,3,5-triphenyl-2H-tetrazolium chloride (TTC) staining; p-Akt/Akt, and p-endothelial nitric oxide synthase (p-eNOS)/eNOS levels were assessed by Western blotting; nitric oxide (NO) content in serum was determined by the Griess reaction. SFI significantly decreased serum CK, LDH and TNNI3 levels in MIRI rats, while it significantly increased the level of left ventricular systolic pressure (LVSP), left ventricular diastolic pressure (LVDP), maximal rate of the increase of left ventricular pressure (+dp/dtmax), maximal rate of the decrease of left ventricular pressure (-dp/dtmax), left ventricle ejection fraction percentage (EF), and stroke volume (SV). In addition, SFI significantly reduced myocardial infarction area and activated the phosphorylation of eNOS via Akt. The phosphorylation of eNOS and the concurrent increase of NO production contributed significantly to the protective effects of SFI. These results demonstrate that SFI protects the rat heart against MIRI and that this effect is mediated in part by Akt/eNOS signaling.
Insights
Shenfu injection (SFI) protects the heart from ischemia-reperfusion injury by activating the Akt/eNOS pathway. This traditional Chinese medicine reduces cardiac damage and improves heart function in rat models.
Area of Science:
- Cardiovascular Pharmacology
- Traditional Chinese Medicine
- Molecular Cardiology
Background:
- Myocardial ischemia-reperfusion injury (MIRI) is a major cause of heart damage.
- Effective therapeutic strategies for MIRI are crucial.
- Shenfu injection (SFI) is a traditional Chinese medicine with potential cardioprotective properties.
Purpose of the Study:
- To investigate the protective effects of Shenfu injection (SFI) against myocardial ischemia-reperfusion injury (MIRI) in a rat model.
- To elucidate the underlying mechanism of SFI's cardioprotective action, focusing on the Akt/eNOS signaling pathway.
Main Methods:
- MIRI was induced in Sprague-Dawley rats by ligating the left anterior descending coronary artery followed by reperfusion.
- Rats were pretreated with SFI or NG-nitro-L-arginine methyl ester (L-NAME).
- Cardiac function, infarct size, serum biomarkers (CK, LDH, TNNI3), nitric oxide (NO) levels, and protein expression (p-Akt/Akt, p-eNOS/eNOS) were assessed.
Main Results:
- SFI significantly reduced serum levels of cardiac injury biomarkers (CK, LDH, TNNI3).
- SFI improved left ventricular function, including increased systolic and diastolic pressures, and enhanced ejection fraction and stroke volume.
- SFI decreased myocardial infarct size and activated the Akt/eNOS signaling pathway, leading to increased NO production.
Conclusions:
- Shenfu injection (SFI) demonstrates significant protective effects against myocardial ischemia-reperfusion injury in rats.
- The cardioprotective mechanism of SFI involves the activation of the Akt/eNOS signaling pathway and subsequent increase in nitric oxide production.
- SFI represents a promising therapeutic agent for managing MIRI.
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