Key result
Thiorphan/irbesartan showed a cardioprotective effect in reducing ischemia-reperfusion injury comparable to nitroglycerin and carvedilol by preserving mitochondrial function and decreasing oxidative stress.
Why the study?
Combined angiotensin receptor neprilysin inhibitors are promising cardioprotective agents, prompting evaluation of thiorphan/irbesartan in myocardial ischemia-reperfusion injury compared to nitroglycerin and carvedilol.
Does thiorphan/irbesartan improve cardiac function and reduce myocardial damage in a rat model of ischemia-reperfusion injury compared to nitroglycerin or carvedilol?
Does thiorphan/irbesartan improve cardiac function and reduce myocardial damage in a rat model of ischemia-reperfusion injury compared to nitroglycerin or carvedilol?
In a rat model of myocardial ischemia-reperfusion injury, thiorphan/irbesartan provided cardioprotection comparable to nitroglycerin and carvedilol, partly by preserving mitochondrial function and reducing oxidative stress.
Should not yet change practice; leaves open whether mitochondrial preservation by thiorphan/irbesartan translates to human ischemia-reperfusion injury.
The combined angiotensin receptor neprilysin inhibitor is a promising cardioprotective pharmacological agent. This study investigated the beneficial effects of thiorphan (TH)/irbesartan (IRB), in myocardial ischemia–reperfusion (IR) injury, compared to each of nitroglycerin and carvedilol. Male Wistar rats were divided into five groups (10 rats/group): Sham, untreated I/R, TH/IRB + IR (0.1/10 mg/kg), nitroglycerin + IR (0.2 mg/kg), and carvedilol + IR (10 mg/kg). Mean arterial blood pressure, cardiac functions and arrhythmia incidence, duration and score were assessed. Cardiac levels of creatine kinase‐MB (CK‐MB), oxidative stress, endothelin‐1, ATP, Na + /K + ATPase pump activity and mitochondria complexes activities were measured. Histopathological examination, Bcl/Bax immunohistochemistry studies and electron microscopy examination of left ventricle were performed. TH/IRB preserved the cardiac functions and mitochondrial complexes activities, mitigated cardiac damage, reduced oxidative stress and arrhythmia severity, improved the histopathological changes and decreased cardiac apoptosis. TH/IRB showed a comparable effect to each of nitroglycerin and carvedilol in alleviating the IR injury consequences. TH/IRB showed significant preservation of mitochondrial complexes activity I and II compared to nitroglycerin. TH/IRB significantly increased LVdP/dtmax and decreased oxidative stress, cardiac damage and endothelin‐1 along with increasing the ATP content, Na + /K + ATPase pump activity and mitochondrial complexes activity when compared to carvedilol. TH/IRB showed a cardioprotective effect in reducing IR injury that is comparable to each of nitroglycerin and carvedilol that could be explained in part by its ability to preserve mitochondrial function, increase ATP, decrease oxidative stress as well as endothelin 1.
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Abdulsalam et al. (2023) studied Myocardial ischemia-reperfusion injury (n=50). Thiorphan/irbesartan vs. Nitroglycerin, carvedilol, untreated I/R, and Sham was evaluated on Cardiac functions, arrhythmia, CK-MB, oxidative stress, endothelin-1, ATP, Na+/K+ ATPase, mitochondria complexes activities, and apoptosis. Thiorphan/irbesartan showed a cardioprotective effect in reducing ischemia-reperfusion injury comparable to nitroglycerin and carvedilol by preserving mitochondrial function and decreasing oxidative stress.
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