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Honokiol Provides Cardioprotection from Myocardial Ischemia/Reperfusion Injury (MI/RI) by Inhibiting Mitochondrial Apoptosis Via the PI3K/AKT Signaling Pathway

Overview
Journal Cardiovasc Ther
Publisher Hindawi
Date 2022 Apr 13
PMID 35414825
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Abstract

Background: Myocardial injury refers to a major complication that occurs in myocardial ischemia/reperfusion injury (MI/RI). Honokiol is a well-recognized active compound extracted from the traditional Chinese herb known as and is utilized in treating different vascular diseases. This research is aimed at examining whether Honokiol might alleviate myocardial injury in an MI/RI model.

Methods: Seventy-eight male C57BL/6 mice were categorized randomly into three cohorts including the Sham operation (Sham) cohort, the MI/RI cohort (Con), and the Honokiol cohort ( = 26 for each cohort). The mice in the Honokiol cohort were treated with Honokiol before MI/RI surgery (0.2 mg/kg/day for 14 days, intraperitoneal), while the mice in the Con cohort were given an intraperitoneal injection with an equivalent volume of vehicle (DMSO) daily in 14 days prior to exposure to MI/RI. After the surgery, creatine kinase- (CK-) MB and cardiac troponin T (cTnT) levels, as well as the infarct area, were measured to assess the degree of myocardial damage. Apoptotic levels were detected using terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining. Electron microscopy was utilized to identify mitochondrial damage. Lastly, the expression levels of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), cleaved caspase-9, cytochrome C (Cyt-C), B cell lymphoma/leukemia-2 (Bcl-2), B cell lymphoma/leukemia-2 associated X (Bax), AKT, p-AKT, PI3K, and p-PI3K were analyzed utilizing western blotting.

Results: Honokiol can reduce the MI/RI-induced cTnT and CK-MB levels, apoptosis index, and mitochondrial swelling in cardiomyocytes via activating the PI3K/AKT signaling pathway.

Conclusion: Honokiol provides cardiac protection from MI/RI by suppressing mitochondrial apoptosis through the PI3K/AKT signaling pathway.

Citing Articles

Mitochondrial apoptosis in response to cardiac ischemia-reperfusion injury.

Wang K, Zhu Q, Liu W, Wang L, Li X, Zhao C J Transl Med. 2025; 23(1):125.

PMID: 39875870 PMC: 11773821. DOI: 10.1186/s12967-025-06136-8.

References
1.
Nazari A, Sadr S, Faghihi M, Azizi Y, Hosseini M, Mobarra N . Vasopressin attenuates ischemia-reperfusion injury via reduction of oxidative stress and inhibition of mitochondrial permeability transition pore opening in rat hearts. Eur J Pharmacol. 2015; 760:96-102. DOI: 10.1016/j.ejphar.2015.04.006. View

2.
Qiu L, Xu R, Wang S, Li S, Sheng H, Wu J . Honokiol ameliorates endothelial dysfunction through suppression of PTX3 expression, a key mediator of IKK/IκB/NF-κB, in atherosclerotic cell model. Exp Mol Med. 2015; 47:e171. PMC: 4525296. DOI: 10.1038/emm.2015.37. View

3.
Kma L, Baruah T . The interplay of ROS and the PI3K/Akt pathway in autophagy regulation. Biotechnol Appl Biochem. 2021; 69(1):248-264. DOI: 10.1002/bab.2104. View

4.
Amani H, Habibey R, Hajmiresmail S, Latifi S, Pazoki-Toroudi H, Akhavan O . Antioxidant nanomaterials in advanced diagnoses and treatments of ischemia reperfusion injuries. J Mater Chem B. 2020; 5(48):9452-9476. DOI: 10.1039/c7tb01689a. View

5.
Wei X, Zhang H, Wei G, Zhang J, DU Y, Tan H . Honokiol Protects against Anti-1-Adrenergic Receptor Autoantibody-Induced Myocardial Dysfunction via Activation of Autophagy. Oxid Med Cell Longev. 2018; 2018:1640804. PMC: 6079338. DOI: 10.1155/2018/1640804. View