Best practices for evaluation of bone marrow in nonclinical toxicity studies

© 2011 by the Authors, Reprinted by Permission of SAGE Publications Inc.

Bibliographische Detailangaben
Veröffentlicht in:Veterinary clinical pathology. - 1975. - 40(2011), 2 vom: 15. Juni, Seite 119-34
1. Verfasser: Reagan, William J (VerfasserIn)
Weitere Verfasser: Irizarry-Rovira, Armando, Poitout-Belissent, Florence, Bolliger, Anne Provencher, Ramaiah, Shashi K, Travlos, Greg, Walker, Dana, Bounous, Denise, Walter, Gail, Bone Marrow Working Group of ASVCP/STP
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2011
Zugriff auf das übergeordnete Werk:Veterinary clinical pathology
Schlagworte:Journal Article
Beschreibung
Zusammenfassung:© 2011 by the Authors, Reprinted by Permission of SAGE Publications Inc.
This manuscript is intended to provide a best practice approach to accurately and consistently assess toxicant-induced bone marrow effects of test articles. In nonclinical toxicity studies, complete blood count data in conjunction with the histological examination of the bone marrow are recommended as the foundation for assessing the effect of test articles on the hematopoietic system. This approach alone can be used successfully in many studies. However, in some situations it may be necessary to further characterize effects on the different hematopoietic lineages, either by cytological or flow cytometric evaluation of the bone marrow. Both modalities can be used successfully, and which one is selected will depend on the expertise, preference of the facility, and the nature of the change in the bone marrow. Other specialized techniques such as clonogenic assays or electron microscopy are used rarely to further characterize hematotoxicity. The indications and techniques to successfully employ histological, cytological, or flow cytometric evaluation as well as clonogenic assays and electron microscopy are reviewed
Beschreibung:Date Completed 21.09.2011
Date Revised 20.10.2016
published: Print
ReprintOf: Toxicol Pathol. 2011 Feb;39(2):435-48. - PMID 21300792
Citation Status PubMed-not-MEDLINE
ISSN:1939-165X
DOI:10.1111/j.1939-165X.2011.00323.x