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Erythrocyte Energy Metabolism in Hereditary Spherocytosis

The incorporation of extracellular orthophosphate-(32)P into cellular ATP, 2,3-diphosphoglyceric acid, and inorganic phosphate has been measured over a period of 6 hours in vitro in red blood cells from normal subjects and from patients with hereditary spherocytosis who had undergone splenectomy. Th...

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Những tác giả chính: Reed, Claude F., Young, Lawrence E.
Định dạng: Bài viết
Ngôn ngữ:en
Được phát hành: 1967
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Truy cập trực tuyến:https://ncbi.nlm.nih.gov/pmc/articles/PMC297119/
https://ncbi.nlm.nih.gov/pubmed/6027083
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id pubmed-297119
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spelling pubmed-2971192004-04-12 Erythrocyte Energy Metabolism in Hereditary Spherocytosis Reed, Claude F. Young, Lawrence E. J Clin Invest Articles The incorporation of extracellular orthophosphate-(32)P into cellular ATP, 2,3-diphosphoglyceric acid, and inorganic phosphate has been measured over a period of 6 hours in vitro in red blood cells from normal subjects and from patients with hereditary spherocytosis who had undergone splenectomy. The pattern of labeling of the intracellular compounds was found to be the same in both types of red blood cells, as reported by other workers using much shorter periods of incubation. In addition, in the present study it was possible to compare the net flux of extracellular phosphate into ATP between the two groups of erythrocytes. These latter results suggest that the actual turnover rate of ATP was not abnormal in these patients with hereditary spherocytosis. 1967-07 /pmc/articles/PMC297119/ /pubmed/6027083 Text en
institution US National Library of Medicine
collection PubMed Central
language en
format Article
topic Articles
spellingShingle Articles
Reed, Claude F.
Young, Lawrence E.
Erythrocyte Energy Metabolism in Hereditary Spherocytosis
description The incorporation of extracellular orthophosphate-(32)P into cellular ATP, 2,3-diphosphoglyceric acid, and inorganic phosphate has been measured over a period of 6 hours in vitro in red blood cells from normal subjects and from patients with hereditary spherocytosis who had undergone splenectomy. The pattern of labeling of the intracellular compounds was found to be the same in both types of red blood cells, as reported by other workers using much shorter periods of incubation. In addition, in the present study it was possible to compare the net flux of extracellular phosphate into ATP between the two groups of erythrocytes. These latter results suggest that the actual turnover rate of ATP was not abnormal in these patients with hereditary spherocytosis.
author Reed, Claude F.
Young, Lawrence E.
author_facet Reed, Claude F.
Young, Lawrence E.
author_sort Reed, Claude F.
title Erythrocyte Energy Metabolism in Hereditary Spherocytosis
title_short Erythrocyte Energy Metabolism in Hereditary Spherocytosis
title_full Erythrocyte Energy Metabolism in Hereditary Spherocytosis
title_fullStr Erythrocyte Energy Metabolism in Hereditary Spherocytosis
title_full_unstemmed Erythrocyte Energy Metabolism in Hereditary Spherocytosis
title_sort erythrocyte energy metabolism in hereditary spherocytosis
publishDate 1967
url https://ncbi.nlm.nih.gov/pmc/articles/PMC297119/
https://ncbi.nlm.nih.gov/pubmed/6027083
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