Continuing Education Course #3

Author:

Bolon Brad1,Garman Robert H.2,Gundersen Hans Jørgen G.3,Allan Johnson G.4,Kaufmann Wolfgang56,Krinke Georg7,Little Peter B.8,Makris Susan L.9,Mellon R. Daniel10,Sulik Kathleen K.11,Jensen Karl12

Affiliation:

1. GEMpath Inc., Longmont, Colorado

2. Consultants in Veterinary Pathology, Murrysville, Pennsylvania

3. University of Aarhus, DK-8000 Aarhus, Denmark

4. Duke University, Durham, North Carolina

5. BASF, Ludwigshafen, Germany

6. *Current address, Merck KGaA, 64293 Darmstadt, Germany

7. Frenkendorf CH-4402, Switzerland

8. Charles River Laboratories Inc., Durham, North Carolina

9. U.S. Environmental Protection Agency (EPA), Washington, DC

10. U.S. Food and Drug Administration (FDA), Silver Spring, Maryland

11. University of North Carolina, Chapel Hill, North Carolina

12. U.S. Environmental Protection Agency, Research Triangle Park, North Carolina

Abstract

The continuing education course on Developmental Neurotoxicity Testing (DNT) was designed to communicate current practices for DNT neuropathology, describe promising innovations in quantitative analysis and noninvasive imaging, and facilitate a discussion among experienced neuropathologists and regulatory scientists regarding suitable DNT practices. Conventional DNT neuropathology endpoints are qualitative histopathology and morphometric endpoints of particularly vulnerable sites (e.g., cerebral, cerebellar, or hippocampal thickness). Novel imaging and stereology measurements hold promise for automated analysis of factors that cannot be effectively examined in routinely processed specimens (e.g., cell numbers, fiber tract integrity). The panel recommended that dedicated DNT neuropathology data sets be acquired on a minimum of 8 sections (for qualitative assessment) or 3 sections (for quantitative linear and stereological analyses) using a small battery of stains to examine neurons and myelin. Where guidelines permit discretion, immersion fixation is acceptable for younger animals (postnatal day 22 or earlier), and peripheral nerves may be embedded in paraffin. Frequent concerns regarding DNT data sets include false-negative outcomes due to processing difficulties (e.g., lack of concordance among sections from different animals) and insensitive analytical endpoints (e.g., qualitative evaluation) as well as false-positive results arising from overinterpretation or misreading by inexperienced pathologists.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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