Marginal copper-restricted diets produce altered cardiac ultrastructure in the rat

Proc Soc Exp Biol Med. 1995 Oct;210(1):43-9. doi: 10.3181/00379727-210-43923.

Abstract

To determine if chronic ingestion of a diet containing a marginally low level of Cu could cause deleterious alterations in cardiac ultrastructure, male offspring were nursed by dams fed a diet containing either 6.7 or 2.8 mg Cu/kg from midgestation through lactation before weaning to the same diet. Conventional measures of Cu status, including growth, relative heart weight, tissue concentrations of Cu, ceruloplasmin activity, and tissue activity of Cu,Zn-superoxide dismutase (SOD) were similar in both dietary treatment groups at 5.5 months of age. However, significant increases in the number and volume of lipid droplets and an increased incidence of pathological abnormalities in mitochondria and basal laminae were observed in sections of hearts from rats chronically fed the diet containing 2.8 mg/kg Cu. Reduction of the dietary level of Cu from 2.8 to 1.3 mg/kg from 4 to 5.5 months of age caused significant reductions in the concentration of Cu in serum and liver, but Cu content, Cu,Zn-SOD activity, pathological scores, and morphometric parameters in hearts were not modified by the greater restriction of dietary Cu in adult rats. This study suggests that abnormalities in cardiac ultrastructure occurred in rats chronically fed diets marginally low in Cu, despite minimal changes in conventional biochemical indicators of Cu status.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Ceruloplasmin / metabolism
  • Copper / administration & dosage*
  • Copper / deficiency
  • Copper / metabolism
  • Diet*
  • Female
  • Lactation
  • Liver / metabolism
  • Male
  • Mitochondria, Heart / pathology
  • Myocardium / metabolism
  • Myocardium / ultrastructure*
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / metabolism
  • Zinc / metabolism

Substances

  • Copper
  • Superoxide Dismutase
  • Ceruloplasmin
  • Zinc