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      Preventive and curative effects of Artemisia absinthium on acetaminophen and CCl4-induced hepatotoxicity.

      General pharmacology
      Acetaminophen, toxicity, Alanine Transaminase, blood, drug effects, Animals, Aspartate Aminotransferases, Carbon Tetrachloride, Dose-Response Relationship, Drug, Drug Synergism, Drug-Induced Liver Injury, Lethal Dose 50, Liver Diseases, enzymology, therapy, Male, Mice, Pentobarbital, pharmacology, Plant Extracts, therapeutic use, Plants, Medicinal, chemistry, Rats, Rats, Wistar, Sleep, Strychnine

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          Abstract

          1. Effect of aqueous-methanolic extract of Artemisia absinthium (Compositae) was investigated against acetaminophen- and CCl4-induced hepatic damage. 2. Acetaminophen produced 100% mortality at the dose of 1 g/kg in mice while pretreatment of animals with plant extract (500 mg/kg) reduced the death rate to 20%. 3. Pretreatment of rats with plant extract (500 mg/kg, orally twice daily for two days) prevented (P < 0.01) the acetaminophen (640 mg/kg) as well as CCl4 (1.5 ml/kg)-induced rise in serum transaminases (GOT and GPT). 4. Post-treatment with three successive doses of extract (500 mg/kg, 6 hr) restricted the hepatic damage induced by acetaminophen (P < 0.01) but CCl4-induced hepatotoxicity was not altered (P > 0.05). 5. Plant extract (500 mg/kg) caused significant prolongation (P < 0.05) in pentobarbital (75 mg/kg)-induced sleep as well as increased strychnine-induced lethality in mice suggestive of inhibitory effect on microsomal drug metabolizing enzymes (MDME). 6. These results indicate that the crude extract of Artemisia absinthium exhibits hepatoprotective action partly through MDME inhibitory action and validates the traditional use of plant in hepatic damage.

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