Reversible Bone Marrow Suppression From Chloramphenicol
- 1 August 1970
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of internal medicine (1960)
- Vol. 126 (2) , 272-275
- https://doi.org/10.1001/archinte.1970.00310080078010
Abstract
Chloramphenicol is a potent inhibitor of mitochondrial protein synthesis. Recent studies on rabbit and human bone marrow mitochondria strongly suggest a relationship between inhibition of protein synthesis and myelotoxicity from chloramphenicol. A thorough electron microscopic study of bone marrow mitochondria derived from patients receiving chloramphenicol indicates that this drug induces ultrastructural modifications resulting in an increase in the density of the mitochondrial matrix. Excellent correlation is observed between the extent of the ultrastructural changes and serum levels of free chloramphenicol. The results lend further support to the hypothesis that reversible bone marrow suppression from chloramphenicol results from inhibition by the drug of mitochondrial protein synthesis.This publication has 4 references indexed in Scilit:
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- Protein synthesis by reticulocyte ribosomes. 3. Description of a ribonucleoprotein fraction which stimulates messenger RNA-ribosomal interaction.Proceedings of the National Academy of Sciences, 1967
- ULTRASTRUCTURAL BASES FOR METABOLICALLY LINKED MECHANICAL ACTIVITY IN MITOCHONDRIAThe Journal of cell biology, 1966
- Avidity of the Tetracyclines for the Cations of MetalsNature, 1956