Modulation of drug-induced hematopoietic toxicity with zinc in murine bone marrow cells (BMC) (Meeting abstract). NLM AIDSLINE Important note: Information in this article was accurate in 1993. The state of the art may have changed since the publication date.

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Modulation of drug-induced hematopoietic toxicity with zinc in murine bone marrow cells (BMC) (Meeting abstract).

Proc Annu Meet Am Assoc Cancer Res; 34:A1700 1993. Unique Identifier : AIDSLINE ICDB/93692641
Gogu SR; Agrawal KC; Dept. of Pharmacology, Tulane Univ. Sch. of Medicine, New; Orleans, LA 70112


Abstract: Drug-induced hematopoietic toxicity is a major limiting factor in the administration of anticancer and anti-HIV drugs. Zinc supplementation has been shown to stimulate immunological function and its deficiency to cause atrophy of the thymus and spleen. We have investigated the role of zinc in reversing zidovudine (AZT)-induced bone marrow toxicity. Murine BMC (1 x 10(6) cells) were exposed to various concentrations (1-20 uM) of AZT in the presence and absence of zinc acetate (100 uM). The cell survival was determined by the colony-forming assays of erythroid (CFU-E) and granulocytic (CFU-GM) lineage. The IC50 values in the presence of zinc were increased approx 3-fold (from 2.4 to 6.6 uM) for CFU-E and 2-fold (for 3.9 to 8.7 uM) for CFU-GM. To delineate the mechanism of this significant protection of BMC, we have monitored the mRNA levels of metallothionein (MT) by using a 31-mer cDNA probe. Zinc produces a concentration-dependent increase in the MT mRNA levels. These results suggest that zinc supplementation can be conveniently used to reduce AZT-induced erythroid toxicity.
Keywords: Animal Bone Marrow Diseases/CHEMICALLY INDUCED/*THERAPY Hematopoietic Stem Cells/*CYTOLOGY Metallothionein/GENETICS Mice RNA, Messenger/METABOLISM Zidovudine/*ADVERSE EFFECTS Zinc/*THERAPEUTIC USE ABSTRACTKWDanimalbonemarrowdiseases/chemicallyinduced/KWDtherapyhematopoieticstemcells/KWDcytologymetallothionein/geneticsmicerna,messenger/metabolismzidovudine/KWDadverseeffectszinc/KWDtherapeuticuseabstract
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M9370995

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