Premium
COMPLETE CEREBRAL ISCHAEMIA IN THE RAT: AN ULTRASTRUCTURAL AND STEREOLOGICAL ANALYSIS OF THE DISTAL STRATUM RADIATUM IN THE HIPPOCAMPAL CA‐1 REGION
Author(s) -
LUBITZ D. K. J. EKSTRÖM VON,
DIEMER N. H.
Publication year - 1982
Publication title -
neuropathology and applied neurobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.538
H-Index - 95
eISSN - 1365-2990
pISSN - 0305-1846
DOI - 10.1111/j.1365-2990.1982.tb00275.x
Subject(s) - hippocampal formation , ultrastructure , synaptic vesicle , stereology , ischemia , hippocampus , stratum , extracellular , biology , synapse , neuroglia , anatomy , chemistry , pathology , neuroscience , central nervous system , vesicle , medicine , membrane , endocrinology , microbiology and biotechnology , biochemistry , paleontology
Ekström von Lubitz D.K.J. & Diemer N.H. (1982) Neuropathology and Applied Neurobiology 8, 197–215 Complete cerebral ischaemia in the rat: an ultrastructural and stereological analysis of the distal stratum radiatum in the hippocampal CA‐1 region An ultrastructural study and a stereological analysis of the distal stratum radiatum in the hippocampal CA‐1 region of the rat were performed after 10 min of complete cerebral ischaemia followed by 10, 20 and 60 min of blood reflow periods. Post‐ischaemic changes were mainly limited to the region of synaptic terminals which showed either clumping or dispersion of the synaptic vesicle pools and damage to synaptic membranes. Presynaptic terminals and astrocytes were swollen after 10 and 20 min of reflow, but this abated after 60 min. Mitochondria in neurons showed varying degrees of swelling, but in astrocytes their structure was normal. There were no changes in capillaries. After 20 and 60 min of blood reflow, disruption of cell membranes was observed, mainly in the vicinity of the synaptic terminals. The size of the extracellular space diminished by approximately 30% in all three ischaemic groups. The data show that synaptic terminals are a primary and early target in the development of postischaemic nerve cell damage.