[Protective effect of cresacin in D-galactosamine-induced acute experimental hepatitis]
- PMID: 9848142
[Protective effect of cresacin in D-galactosamine-induced acute experimental hepatitis]
Abstract
Antioxidant properties of cresacin were studied on the model of galactosamine hepatitis and on the isolated liver cells of white male rats. It has been shown, that cresacin in a dose of 20 mg/kg effectively inhibits the processes of lipid peroxidation induced by hepatotoxin. Cresacin also normalized some components of fermentative and non-enzymatic antioxidant system. In particular the indexes of the activity of superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase and the level of reduced glutathione, total phospholipids and ascorbic acid was increased for certain. In vitro, on the isolated hepatocytes, cresacin showed the dose-dependent antioxidant effect. This fact is confirmed by its property to inhibit the speed of formation of the malonic dialdehyde in the incubation medium.
Similar articles
-
Xanthine oxidase-derived reactive oxygen species contribute to the development of D-galactosamine-induced liver injury in rats.Free Radic Res. 2007 Feb;41(2):135-44. doi: 10.1080/10715760600953842. Free Radic Res. 2007. PMID: 17364939
-
Effect of Indigofera tinctoria Linn on liver antioxidant defense system during D-galactosamine/endotoxin-induced acute hepatitis in rodents.Indian J Exp Biol. 2001 Feb;39(2):181-4. Indian J Exp Biol. 2001. PMID: 11480218
-
[Immunomodulating and hepatoprotective action of retinoids in toxic liver involvement induced by D-galactosamine].Antibiot Khimioter. 1996;41(7-8):22-5. Antibiot Khimioter. 1996. PMID: 8999757 Russian.
-
[Pharmacologic regulation of hepatocyte cytolysis by antioxidants during acute D-galactosamine hydrochloride intoxication].Biull Eksp Biol Med. 1998 Apr;125(4):417-9. Biull Eksp Biol Med. 1998. PMID: 9631725 Russian. No abstract available.
-
Diethyldithiocarbamate inhibition of galactosamine-induced hepatitis in rats.Pharmacol Res. 2002 Mar;45(3):253-5. doi: 10.1006/phrs.2001.0940. Pharmacol Res. 2002. PMID: 11884224
MeSH terms
Substances
LinkOut - more resources
Medical