Table 3.
The molecular and cellular mechanisms underlying the cardioprotection of melatonin treatment in myocardial I/R injury.
Studies | Year | Proposed mechanisms |
---|---|---|
Chen et al. | 2018 | Inhibit autophagy via AMPK/mTOR signaling pathway |
Zhou et al. | 2017 | Attenuate FUNDC1-required mitophagy, inflammation, improve microvascular function via regulating the expression of platelet PPARγ |
Zhai et al. | 2017 | Antioxidative stress, antiapoptosis through activation of SIRT3 signaling pathway |
Zhou et al. | 2017 | Regulate mitochondrial fission, mitophagy, mPTP opening, and HK2-VDAC1 interaction |
He et al. | 2016 | Restore autophagy function, suppress oxidative stress and apoptosis through nuclear receptor RORα |
Yu et al. | 2015 | Notch1/Hes1 signaling and Pten/Akt signaling underlie the antioxidative stress and antiapoptosis effect |
Yu et al. | 2014 | Reduce apoptosis and oxidative damage via SIRT1 signaling |
Chen et al. | 2009 | Attenuate apoptosis independent of Gpx1 |
Genade et al. | 2008 | Antiadrenergic actions mediated by NO and PKC signaling, PKB/Akt activation, and p38MAPK signaling involved in the cardioprotection |
Lochner et al. | 2006 | NA |
Sahna et al. | 2004 | Attenuate oxidative stress (reduce MDA and restore GSH level) |
Sahna et al. | 2002 | NA |
Lee et al. | 2002 | Antioxidant activity, inhibit neutrophil infiltration |
Lagneux et al. | 2000 | NA |
Nduhirabandi et al. | 2010 | Prevent metabolic abnormality via modulating insulin release and PKB/Akt and ERK 1/2 signaling |