Table 5.
The effects of melatonin on atherosclerosis and intimal hyperplasia.
Drug or pharmacological agent | Melatonin dose | Treatment duration | Targets | Effects | Model | References |
---|---|---|---|---|---|---|
Melatonin | 10 mg/kg/d | 4 weeks | VEGF, eNOS, Nrf2/ROS/NLRP3 signaling pathway | Reduced rat carotid artery intimal hyperplasia, attenuated smoking-induced atherosclerosis | In vivo (rats) | (391) |
Melatonin | 5, 10 mg/kg/d | 2 weeks | Vaspin, visfatin, DDAH, STAT-3 | Protected against atherosclerosis, anti-inflammatory effects | In vivo (rats) | (416) |
Melatonin | 10 mg/kg/d | 12 weeks | HGF/c-Met axis | Reduced number of macrophages in plaque, increased stability | In vivo (rabbits) | (406) |
Melatonin | 10 mg/kg/d | 9 weeks | RORα, AMPKα-STAT pathway | Regulated plaque inflammation, increased plaque stability | In vivo (mice) | (393) |
Melatonin | 0.3, 3, 30 mg/kg/d | 8 weeks | P4Hα1, Akt, Sp1 | Stabilized plaque | In vitro, in vivo (mice) | (394) |
Melatonin | 10 mg/kg/d | 7, 15 weeks | TNF-α, PDGF-BB | Suppressed atherosclerosis | In vitro, in vivo (mice) | (396) |
Melatonin | 20 mg/kg/d | 4 weeks | NLRP3, Sirt3/FOXO3a/Parkin signaling pathway | Inhibited progression of atherosclerosis | In vitro, in vivo (mice) | (417) |
Melatonin | 20 mg/kg/d | 4 weeks | Myosin light chain kinase (MLCK), ERK, JNK, p38 | Inhibited atherosclerosis | In vivo (rabbits) | (418) |
Melatonin | 10 mg/kg/d | 12 weeks | TLR4, MyD88, NF-κB, p65, IκB | Improved endothelial function, suppressed plaque formation | In vivo (rabbits) | (377) |
DTBHB | 0.02% wt/wt | 16-weeks | IL-6, TNFa | Did not modify atherosclerosis | In vivo (mice) | (419) |
Melatonin | 0.02% (w/w) | 16 weeks | – | Increased atherosclerosis | In vivo (mice) | (420) |