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NADPH‐Diaphorase histochemistry in the postnatal mouse cerebellum suggests specific developmental functions for nitric oxide
Author(s) -
Brüning G.
Publication year - 1993
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.490360510
Subject(s) - cerebellum , colocalization , granular layer , nadph dehydrogenase , nitric oxide , nitric oxide synthase , purkinje cell , granule cell , calbindin , staining , biology , immunohistochemistry , white matter , chemistry , anatomy , microbiology and biotechnology , biophysics , central nervous system , neuroscience , endocrinology , immunology , medicine , dentate gyrus , genetics , radiology , magnetic resonance imaging
NADPH‐diaphorase histochemistry has been applied for the localization of nitric oxide synthase during the postnatal development of the mouse cerebellum. Staining for NADPH‐diaphorase during the first week after birth was confined to some but not all laminae of the immature cerebellum: NADPH‐diaphorase activity was located in the molecular/Purkinje cell layer and in inner parts of the internal granular layer. The external granular layer and the developing white matter were essentially unstained. Expression was earliest and very strong in parallel fibers and in the internal granule layer of the ventral part of the pyramis and the dorsal part of the uvula. Staining in the Purkinje cell layer was observed throughout the cerebellum. The presence of formazan deposits within Purkinje cells was verified by colocalization with calbindin D‐28k immunoreactivity. The distribution of NADPH‐diaphorase activity changed into the adult pattern between 8 and 12 days of age: Within the molecular layer, basket cells and their processes became strongly stained. Reaction product within Purkinje cells gradually disappeared. Likewise, strongly stained parallel fibers were no longer detectable. These results suggest that nitric oxide is involved in different processes in cerebellar development. © 1993 Wiley‐Liss, Inc.