Exendin-4 Ameliorates Cardiac Remodeling in Experimentally Induced Myocardial Infarction in Rats by Inhibiting PARP1/NF-κB Axis in A SIRT1-Dependent Mechanism.
Refaat A EidSamah A AlharbiAttalla Farag El-KottSamy M EleawaMohamed Samir Ahmed ZakiFahmy El-SayedMuhammad Alaa EldeenHussain AlderaAbd Al-Rahman Salem Al-ShudiefatPublished in: Cardiovascular toxicology (2021)
Sirt1 is a potent inhibitor of both poly(ADP-ribose) polymerases1 (PARP1) and NF-kB. This study investigated the cardioprotective effect of exendin-4 on cardiac function and remodeling in rats after an expreimentally-induced myocardial infarction (MI) and explored if this protection involves SIRT1/PARP1 axis. Rats were divided into five groups (n = 10/each): sham, sham + exendin-4 (25 nmol/kg/day i.p.), MI (induced by LAD occlusion), MI + exendin-4, and sham + exendin-4 + EX527 (5 mg/2×/week) (a SIRT1 inhibitor). All treatments were given for 6 weeks post the induction of MI. In sham-operated and MI-induced rats, exendin-4 significantly upregulated Bcl-2 levels, enhanced activity, mRNA, and levels of SIRT1, inhibited activity, mRNA, and levels of PARP1, and reduced ROS generation and PARP1 acetylation. In MI-treated rats, these effects were associated with improved cardiac architectures and LV function, reduced collagen deposition, and reduced mRNA and total levels of TNF-α and IL-6, as well as, the activation of NF-κB p65. In addition, exendin-4 inhibited the interaction of PARP1 with p300, TGF-β1, Smad3, and NF-κB p65 and signficantly reduced mRNA and protein levels of collagen I/III and protein levels of MMP2/9. In conclusion, exendin-4 is a potent cardioprotective agent that prevents post-MI inflammation and cardiac remodeling by activating SIRT1-induced inhibition of PARP1.
Keyphrases
- oxidative stress
- dna damage
- diabetic rats
- signaling pathway
- dna repair
- high glucose
- left ventricular
- ischemia reperfusion injury
- lps induced
- binding protein
- pi k akt
- cell death
- randomized controlled trial
- drug induced
- double blind
- epithelial mesenchymal transition
- transforming growth factor
- mouse model
- endothelial cells
- cell proliferation
- reactive oxygen species
- small molecule
- atrial fibrillation
- stress induced