DOI: 10.5176/2345-7201_1.2.18

Authors:  Umbreen Ahmed, Trevor G. Redgrave and Phillip S. Oates (ret)


The liver is the major site for lipoprotein processing and iron storage. Non-alcoholic fatty liver disease (NAFLD) is a broad spectrum of chronic liver disorder with progressive factors hypothesized to include impaired hepatic lipid metabolism and oxidative stress. Since iron produces oxidative stress, its excess may lead to lipid peroxidation and hepatocyte damage. We hypothesized that increased hepatic iron in rats fed a western diet would progress NAFLD. We determined the effect of variation in iron on plasma and hepatic lipids and oxidative stress in a rat model without pre-existing liver damage. Rats were fed liquid diets in which 35{6e6090cdd558c53a8bc18225ef4499fead9160abd3419ad4f137e902b483c465} of the energy was fat and contained low (STD-), normal (STD) or twice the normal level (STD+) of iron. The STD+ group also received parenteral iron dextran injections. After 5 weeks liver and blood were taken for analysis. Serum cholesterol and non-esterified fatty acids were increased in STD+ compared with STD group. Serum triglyceride in STD+ rats was increased compared with STD-. Histologically the STD+ group showed foci of macrovesicular lipid droplets, whereas hepatic triglyceride was decreased in STD-. Liver expression of lipid responsive gene (SREBP-2, SREBP-1c, HMG CoA reductase, 7α hydroxylase, MTTP1), chemokine (MCP-1) and oxidative stress marker, haemoxygenase-1 mRNA were similar in all groups. There were significant increases in hepatic malondialdehyde and hydroxyalkenal in STD+ compared with STD group. The erythrocytes of STD+ were osmotically fragile compared with the STD group. Increased liver iron affects plasma and hepatic lipids and may progress NAFLD by impairing hepatic fat metabolism.

Keywords: Dietary fat, iron, iron dextran, rat model, non-alcoholic fatty liver disease

Price: $0.00

Loading Updating cart...