Metabolism - Clinical and Experimental
Volume 46, Issue 4 , Pages 377-381, April 1997

Hepatic iron overload may contribute to hypertriglyceridemia and hypercholesterolemia in copper-deficient rats

  • Meira Fields

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Meira Fields, PhD, USDA, ARS, BHNRC, Metabolism and Nutrient Interactions Laboratory, Room 323, Bldg 307, BARC-East, Beltsville, MD 20705.
  • ,
  • Charles G. Lewis

Metabolism and Nutrient Interactions Laboratory, Beltsville Human Nutrition Research Center, US Department of Agriculture, Agricultural Research Service, Beltsville, MD, USA

Received 17 June 1996; accepted 11 September 1996.

Abstract 

The present study was conducted in order to determine whether hepatic iron retention in rats fed a copper-deficient diet containing fructose is associated with hypertriglyceridemia and hypercholesterolemia, and whether a reduction of iron intake will prevent elevation of blood triglycerides and cholesterol. Rats were fed from weaning either a copper-deficient (0.6 μg Cu/g) or copper-adequate (6.0 μg Cu/g) diet for 4 weeks. Half the rats consumed either an adequate level of iron (50 μg Fe/g) or a low level (17 μg Fe/g). Reduction of iron intake reduced blood levels of both triglycerides and cholesterol in rats fed a copper-deficient diet containing fructose. In addition, hepatic lipid peroxidation was also decreased. The combination of high iron, low copper, and fructose may be responsible for increased levels of risk-factor metabolites associated with heart disease.

No full text is available. To read the body of this article, please view the PDF online.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0026-0495(97)90051-2

Metabolism - Clinical and Experimental
Volume 46, Issue 4 , Pages 377-381, April 1997