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Protective effects of 5-methoxypsoralen against acetaminophen-induced hepatotoxicity in mice
Wei-Xia Liu1, Feng-Lan Jia, Yue-Ying He
1Department of Toxicology, School of Public Health, Peking University, Beijing 100191, China.
Aim:
To investigate the hepatic protective effects of 5-methoxypsoralen (5-MOP) and to learn if 5-MOP causes hepatotoxicity at protective doses.
Methods:
C57BL/6J mice were administrated orally with 5-MOP at doses of 12.5, 25 and 50 mg/kg body weight respectively every morning for 4 d before given acetaminophen (APAP) subcutaneously at a dose of 500 mg/kg. The 5-MOP alone group was treated with 5-MOP orally at a dose of 50 mg/kg body weight for 4 d without APAP. Twenty-four hours after APAP administration, blood samples of mice were analyzed for serum enzyme alanine transaminase (ALT), aspartate transaminase (AST), lactate dehydrogenase (LDH) levels, and malondialdehyde (MDA), reduced glutathione (GSH) and oxidized glutathione (GSSG) of liver tissues were measured and histopathologic changes of the liver were observed.
Results:
Compared with the vehicle control group, the serum levels (IU/L) of ALT, AST and LDH were all increased significantly in APAP group (8355 ± 3940 vs 30 ± 21, P < 0.05; 6482 ± 4018 vs 146 ± 58, P < 0.05; 24627 ± 10975 vs 1504 ± 410, P < 0.05). Compared with APAP group, the serum ALT levels (IU/L) (1674 ± 1810 vs 8355 ± 3940, P < 0.05; 54 ± 39 vs 8355 ± 3940, P < 0.05; 19 ± 9 vs 8355 ± 3940, P < 0.05), AST levels (IU/L) (729 ± 685 vs 6482 ± 4108, P < 0.05; 187 ± 149 vs 6482 ± 4108, P < 0.05; 141 ± 12 vs 6482 ± 4108, P < 0.05) and LDH levels (IU/L) (7220 ± 6317 vs 24 627 ± 10 975, P < 0.05; 1618 ± 719 vs 24 627 ± 10 975, P < 0.05; 1394 ± 469 vs 24 627 ± 10 975, P < 0.05) were all decreased drastically in the three-dosage 5-MOP pretreatment groups. Pretreatment of 5-MOP could attenuate histopathologic changes induced by APAP, including hepatocellular necrosis and infiltration of inflammatory cells, and the effect was dose-dependent. MDA levels (nmol/mg) were decreased by 5-MOP in a dose-dependent manner (0.98 ± 0.45 vs 2.15 ± 1.07, P > 0.05; 0.59 ± 0.07 vs 2.15 ± 1.07, P < 0.05; 0.47 ± 0.06 vs 2.15 ± 1.07, P < 0.05). The pretreatment of 5-MOP could also increase the GSH/GSSG ratio (3.834 ± 0.340 vs 3.306 ± 0.282, P > 0.05; 5.330 ± 0.421 vs 3.306 ± 0.282, P < 0.05; 6.180 ± 0.212 vs 3.306 ± 0.282, P < 0.05). In the group treated with 5-MOP but without APAP, the serum enzyme levels, the liver histopathologic manifestation, and the values of MDA and GSH/GSSG ratio were all normal.
Conclusion:
5-MOP can effectively protect C57BL/6J mice from APAP-induced hepatotoxicity and possesses an antioxidative activity, and does not cause liver injury at the protective doses.
Insights
5-methoxypsoralen (5-MOP) protects mice from acetaminophen-induced liver injury by reducing harmful enzymes and oxidative stress. Importantly, 5-MOP does not cause liver damage at these protective doses.
Area of Science:
- Pharmacology
- Hepatology
- Toxicology
Background:
- Acetaminophen (APAP) overdose is a leading cause of acute liver failure.
- Hepatoprotective agents are crucial for managing APAP-induced liver injury.
- 5-methoxypsoralen (5-MOP) is a naturally occurring compound with potential therapeutic properties.
Purpose of the Study:
- To evaluate the hepatoprotective effects of 5-methoxypsoralen (5-MOP) against acetaminophen (APAP)-induced liver damage.
- To determine if 5-MOP exhibits hepatotoxicity at effective protective doses.
Main Methods:
- C57BL/6J mice were pretreated with varying doses of 5-MOP (12.5, 25, 50 mg/kg) before APAP administration.
- Serum levels of liver enzymes (ALT, AST, LDH) were measured.
- Liver tissues were analyzed for oxidative stress markers (MDA, GSH/GSSG ratio) and histopathological changes.
Main Results:
- 5-MOP pretreatment significantly reduced APAP-induced elevations in ALT, AST, and LDH levels in a dose-dependent manner.
- 5-MOP attenuated liver histopathological damage, including hepatocellular necrosis and inflammation.
- 5-MOP increased the GSH/GSSG ratio and decreased MDA levels, indicating reduced oxidative stress.
- No hepatotoxicity was observed in mice treated with 5-MOP alone.
Conclusions:
- 5-methoxypsoralen (5-MOP) demonstrates significant hepatoprotective effects against APAP-induced liver injury in mice.
- 5-MOP exhibits antioxidative properties, contributing to its protective mechanism.
- The study confirms that 5-MOP is safe at protective doses, showing no evidence of hepatotoxicity.
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