British Journal of Pharmacology · 2001 · 51 citations · 9 references
PharmacyPharmacologyToxicologyClinical PharmacologyHepatotoxicologyPharmaceutical ToxicologyBiomarkers Of Liver InjuryHepatic ToxicityHepatotoxicity MechanismsAspartate Aminotransferase ElevationGlutamate DehydrogenaseHepatoprotective AgentsLiver Injury MechanismsNitric OxideParacetamol ToxicitySerum Alanine AminotransferaseSerum Aspartate Aminotransferase
Paracetamol (5 mmol kg(-1), i.p.) caused liver damage in rats as indicated by increased plasma aspartate aminotransferase (AST), alanine aminotransferase (ALT) and glutamate dehydrogenase (GDH) activities. No change in plasma bilirubin or creatinine was noted. An equimolar dose of nitroparacetamol (a nitric oxide (NO)-releasing derivative of paracetamol) did not alter plasma levels of any of the markers of liver/kidney damage. No difference in plasma or liver paracetamol was apparent in animals injected with paracetamol or nitroparacetamol. These results indicate that NO released from nitroparacetamol exhibits hepatoprotective activity in these animals and suggest that nitroparacetamol may therefore be considered as a safer alternative to paracetamol in the clinic.
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Role of nitric oxide in acetaminophen-induced hepatotoxicity in the rat
Carol R. Gardner, Diane E. Heck, Paul E. Thomas et al. · Hepatology · 1998 · 258 citations
Csaba Szabó, Ruslana Bryk, Basilia Zingarelli et al. · British Journal of Pharmacology · 1996 · 58 citations · Full text
Nitroparacetamol exhibits anti‐inflammatory and anti‐nociceptive activity
O A Al‐Swayeh, L E Futter, R H Clifford et al. · British Journal of Pharmacology · 2000 · 56 citations · Full text