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PMID: 3214745 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Videomicroscopy of acute brain slices from amygdala and hippocampus.

Brain research bulletin ·Vol. 21 ·No. 3 ·1988-09-00 ·Pages 373-83

Keenan CL, Chapman PF, Chang VC, Brown TH

Abstract

Video-enhanced contrast, differential-interference contrast microscopy (VEC-DICM) was used to visualize the cytoarchitecture and subcellular neuronal structure of acute brain slices from rat hippocampus and amygdala. Even at low-power magnification, the VEC-DICM system vastly improved our ability to visualize and examine the gross organization of the tissue. With medium-power magnification, the neuronal somata and proximal dendrites were clearly visible. With high-power magnification, some of the subcellular details could be clearly discerned--including cell nuclei, cell nucleoli, fine dendritic processes, and varicosities that may be synaptic expansions. We conclude that improved optical techniques should be valuable to cellular neurobiologists interested in structure-function relationships in brain slices.

MeSH Terms
Aging/physiology Amygdala/cytology,growth & development Animals Hippocampus/cytology,growth & development Microscopy/methods Rats Videotape Recording
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Keenan C L
Division of Neurosciences, Beckman Research Institute of the City of Hope, Duarte, CA 91010.
Chapman P F
Chang V C
Brown T H
Article Info
Journal
Brain research bulletin
Abbr.
Brain Res Bull
ISSN
0361-9230
Published
1988-09-00
Pages
373-83
Language
English
Region
United States
NLM ID
7605818
Subset
IM
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