Free radical scavenging and hepatoprotective activity of jigrine against galactosamine induced hepatopathy in rats
Introduction
Jigrine is a polypharmaceutical herbal formulation containing aqueous extracts of 14 medicinal plants used for liver ailments (Table 1). Few studies are reported for its formulation (Najmi et al., 2002), safety evaluation (Valecha et al., 1990), mechanism of hepatoprotective action (Vivek et al., 1994, Karunakar et al., 1997a, Aftab et al., 1999) and anti-inflammatory activity (Karunakar et al., 1997b). Hepatoprotective and anti-inflammatory effects of some of the individual ingredients of jigrine are also reported in literature (Jindal et al., 1975, Sadique et al., 1987, Chawla et al., 1992, Gilani and Aftab, 1992, Gilani et al., 1993, Reddy et al., 1993, Gilani and Janbaz, 1994, Pandey et al., 1994, Sultana et al., 1995, Zafar and Ali, 1998).
The present study is designed to investigate the DPPH-free radical scavenging activity, hepatoprotective and antioxidant activity of jigrine against galactosamine induced hepatotoxicity in rats.
Section snippets
Drugs and chemicals
Jigrine was provided by Hamdard (Wakf) Labs., Ghaziabad, India. Jigrine contains aqueous extract of 14 medicinal plants (Table 1). These constituent plants were collected and authenticated by taxonomist at the Hamdard (Wakf) Labs. The extract was prepared from the freshly collected plant materials. Silymarin was purchased from Micro Labs., Holar, TN, India. Galactosamine was procured from SRL, India. All the biochemicals and chemicals used were of analytical grade.
Animals
Wistar strain albino rats
Biochemical observations
A significant increase (P < 0.01) in serum AST, ALT, urea and tissue TBARS levels was observed in animals treated with galactosamine (Group II) as compared to normal control group (Group I). Jigrine (1 ml/kg, p.o.) pre-treatment for 21 days decreased the levels of above indices significantly (P < 0.01) in Groups III and IV. Moreover, the galactosamine induced significant decrease (P < 0.05) in blood glutathione and tissue glutathione was also significantly increased (P < 0.05) by jigrine pre-treatment.
Discussion
Galactosamine induced experimental model system in rats is recognized to be much like viral hepatitis in humans from both morphological and functional points of view (Keppler et al., 1968). Galactosamine has great liver specificity because hepatocytes have high levels of galactokinase and galactose-1-uridyltransferase. Galactosamine does not affect other organs (Maley et al., 1968, Keppler et al., 1970). Galactosamine causes hepatic injury with spotty hepatocytes necrosis and marked portal and
Acknowledgement
Authors are thankful to Hamdard (Wakf) Labs, Ghaziabad, for providing generous gift sample of jigrine.
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