Protective effects of melatonin and L-carnitine against methotrexate-induced toxicity in isolated rat hepatocytes.
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
melatonin (MEL) and/or L-carnitine (L-CAR) | decrease | hepatocyte toxicity | isolated rat hepatocytes | - | significantly protected hepatocytes against toxicity | #1 |
melatonin (MEL) and/or L-carnitine (L-CAR) | decrease | lipid peroxidation (LPO) levels | isolated rat hepatocytes | - | decreased | #2 |
melatonin (MEL) and/or L-carnitine (L-CAR) | decrease | nitric oxide (NO) levels | isolated rat hepatocytes | - | decreased | #3 |
melatonin (MEL) and/or L-carnitine (L-CAR) | decrease | tumor necrosis factor-alpha (TNF-α) levels | isolated rat hepatocytes | - | decreased | #4 |
melatonin (MEL) and/or L-carnitine (L-CAR) | decrease | caspase-3 activity | isolated rat hepatocytes | - | decreased | #5 |
melatonin (MEL) and/or L-carnitine (L-CAR) | increase | glutathione (GSH) level | isolated rat hepatocytes | - | increased | #6 |
melatonin (MEL) and/or L-carnitine (L-CAR) | decrease | hepatocytotoxicity | isolated rat hepatocytes | - | prevented MTX-induced hepatocytotoxicity | #7 |
The present study was designed to evaluate the possible protective effects of melatonin (MEL) and/or L-carnitine (L-CAR) against methotrexate (MTX)-induced toxicity in isolated rat hepatocytes. Hepatocytes were prepared using collagenase techniques of perfusion and digestion of rat liver. Trypan blue uptake, as well as, glutathione (GSH), lipid peroxidation (LPO), nitric oxide (NO), and tumor necrosis factor-alpha (TNF-α) levels were measured. Caspase-3 activity was also assessed. Pre-incubation of hepatocytes with MEL (1 mM) and/or L-CAR (10 mM) 30 min prior to intoxication with MTX, significantly protected hepatocytes against toxicity. In addition, LPO, NO, TNF-α levels, and caspase-3 activity were decreased in comparison to the MTX-intoxicated group. Furthermore, the two drugs increased the MTX-depleted GSH level. MEL and L-CAR prevented MTX-induced hepatocytotoxicity, at least partly, by their antioxidative, antiinflammatory, and antiapoptotic effects. Further studies are recommended on the clinical pharmacologic and toxicologic effects of MEL and L-CAR in patients receiving MTX.