» Articles » PMID: 13319587

Studies on Copper Metabolism. XIX. The Kinetics of Iron Metabolism and Erythrocyte Life-span in Copper-deficient Swine

Overview
Journal J Exp Med
Date 1956 May 1
PMID 13319587
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Ferrokinetic studies were performed in three copper-deficient swine and the results have been compared with similar studies in 18 normal pigs. The mean value for the plasma iron turnover rate in the deficient swine was 1.76 mg./kg. day; for the red cell iron incorporation rate, 1.24 mg./kg. day; for the red cell iron turnover rate, 1.18 mg./kg. day; for the red cell life span, 13 days. Corresponding figures in the normal swine were 1.11 mg./kg. day, 1.01 mg./kg. day, 0.59 mg./kg. day and 63 days, respectively. The red cell life span was measured by the use of radioactive chromium in a total of 26 pigs. The mean erythrocyte half-life of normal cells transfused into normal pigs was 17 days. The mean half-life of erythrocytes from copperdeficient swine transfused into copper-deficient swine was 9 days. The mean half-life of red cells from control animals transfused into copper-deficient swine was 16 days while that of erythrocytes from copper-deficient swine transfused into normal pigs, was 13 days. The mean half-life of cells from iron-deficient pigs transfused into iron-deficient pigs was 19 days. It is concluded that copper deficiency anemia results from both a shortened erythrocyte survival time and limited capacity of the bone marrow to produce red cells. It is suggested that copper is an essential component of erythrocytes in swine.

Citing Articles

Experimental production of siderocytes.

Deiss A, Kurth D, CARTWRIGHT G, Wintrobe M J Clin Invest. 1966; 45(3):353-64.

PMID: 5948296 PMC: 292705. DOI: 10.1172/JCI105350.


Iron metabolism in copper-deficient swine.

Lee G, NACHT S, Lukens J, CARTWRIGHT G J Clin Invest. 1968; 47(9):2058-69.

PMID: 5675426 PMC: 297366. DOI: 10.1172/JCI105891.


The role of ceruloplasmin in iron metabolism.

Roeser H, Lee G, NACHT S, CARTWRIGHT G J Clin Invest. 1970; 49(12):2408-17.

PMID: 5480864 PMC: 322742. DOI: 10.1172/JCI106460.


[Glutathione peroxidase: enzymology and biological aspects].

Flohe L Klin Wochenschr. 1971; 49(12):669-83.

PMID: 4932493 DOI: 10.1007/BF01487101.


Anemia associated with changes in iron and iron-59 utilization in copper deficient rats fed high levels of dietary ascorbic acid and iron.

Johnson M, Murphy C Biol Trace Elem Res. 1988; 17:69-80.

PMID: 2484369 DOI: 10.1007/BF02795447.


References
1.
LAHEY M, GUBLER C, CHASE M, CARTWRIGHT G, Wintrobe M . Studies on copper metabolism. II. Hematologic manifestations of copper deficiency in swine. Blood. 1952; 7(11):1053-74. View

2.
GUBLER C, LAHEY M, CHASE M, CARTWRIGHT G, Wintrobe M . Studies on copper metabolism. III. The metabolism of iron in copper deficient swine. Blood. 1952; 7(11):1075-92. View

3.
Read R . Studies of red-cell volume and turnover using radiochromium; description of a new closed method of red-cell volume measurement. N Engl J Med. 1954; 250(24):1021-7. DOI: 10.1056/NEJM195406172502402. View

4.
Mollison P, VEALL N . The use of the isotope 51Cr as a label for red cells. Br J Haematol. 1955; 1(1):62-74. DOI: 10.1111/j.1365-2141.1955.tb05489.x. View

5.
Bush J, MAHONEY J, Markowitz H, GUBLER C, CARTWRIGHT G, Wintrobe M . Studies on copper metabolism. XIV. Radioactive copper studies in normal subjects and in patients with hepatolenticular degeneration. J Clin Invest. 1955; 34(12):1766-78. PMC: 438760. DOI: 10.1172/JCI103232. View