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Cytology and synaptology of the lateral reticular nucleus of the cat
Author(s) -
Hrycyshyn A. W.,
Flumerfelt B. A.
Publication year - 1981
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.901970308
Subject(s) - dendritic spine , biology , ultrastructure , golgi apparatus , reticular formation , reticular connective tissue , appendage , synaptic vesicle , anatomy , vesicle , soma , nucleus , spine (molecular biology) , neuroscience , synapse , microbiology and biotechnology , endoplasmic reticulum , genetics , hippocampal formation , membrane
The organization of the lateral reticular nucleus (LRN) of the cat was investigated using electron microscopic and Golgi techniques. Golgi‐Cox preparations revealed that the LRN consists of allodendritic and, especially, isodendritic neurons. The latter have been associated with neural centres that have important roles integrating signals from distant sources. Several froms of spines were identified with the Golgi method, and their ultrastructural correlates were determined. Somatic spines resembled stubby protrusions, while dendritic spines, which were usually observed on distal dendrites, appeared as pedunculated spines, recemose appendages and spine‐crowned appendages. Ultrastructural exmaination of this nucleus revealed various synaptic relationships. The majority of the synaptic terminals were small (1.5–2.5 μm in diameter), contained round vesicles and usually contacted dendrites and spines. Other small terminals contained pleomorphic vesicles and contacted distal dendrites and spines. Large terminals (>2.5 μm in diameter) with round or pleomorphic vesicles contacted the somata or proximal dendrites. Three types of “synaptic configurations,” which consisted of discrete aggregations of neuronal processes invested by astrocytic lamellae, were also identified. These structural arrangements likely provide a basis for the integration of inputs to the LRN from spinal and supraspinal centres.