CEREBELLAR INJURY INDUCES NADPH DIAPHORASE IN PURKINJE AND INFERIOR OLIVARY NEURONS IN THE RAT

被引:43
作者
CHEN, S
ASTONJONES, G
机构
[1] Division of Behavioral Neurobiology, Department of Mental Health Sciences, Hahnemann University, Philadelphia, PA 19102, Broad and Vine
关键词
D O I
10.1006/exnr.1994.1064
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
NADPH diaphorase (NADPH-D) histochemistry was examined following cerebellar lesions induced by stab or knife cuts. A population of Purkinje cells adjacent to the injury became NADPH-D positive after either type of lesion. These cells appeared by 3 days postlesion and were still seen after 6 weeks. Somata of reactive cells shrank gradually and were reduced about 38% in size by 6 weeks after lesion. In the inferior olive of animals subjected to cerebellar knife cut, NADPH-D-positive cells were found in the beta nucleus, dorsal cap, and subnucleus C. These cells became NADPH-D positive 5 days postlesion, were shrunken at 4 weeks postlesion, and were reduced about 26% in somata size by 6 weeks after lesion. Other cerebellar afferents did not exhibit obvious NADPH-D induction following these lesions. In unlesioned animals, no Purkinje cells or inferior olivary neurons were NADPH-D positive. The present study demonstrates that cerebellar damage induces NADPH-D, a marker for nitric oxide (NO) synthase, in Purkinje cells and inferior olivary neurons. In addition, these reactive neurons exhibit long-term degenerative changes. Taken together with previous studies, these findings indicate that NO, produced by the lesion-induced nitric oxide synthase (NOS), may contribute to the degeneration of brain neurons after injury. The lack of NADPH-D-positive neurons in either Purkinje or the inferior olivary neurons in non-lesioned animals indicates that this may provide a useful model system to study injury-induced NOS in brain. (C) 1994 Academic Press, Inc.
引用
收藏
页码:270 / 276
页数:7
相关论文
共 28 条
[1]   COLUMNAR ORGANIZATION OF THE INFERIOR OLIVE PROJECTION TO THE POSTERIOR LOBE OF THE RAT CEREBELLUM [J].
APPS, R .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 302 (02) :236-254
[2]   INFERIOR OLIVARY NUCLEAR-COMPLEX OF THE RAT - MORPHOLOGY AND COMMENTS ON THE PRINCIPLES OF ORGANIZATION WITHIN THE OLIVOCEREBELLAR SYSTEM [J].
AZIZI, SA ;
WOODWARD, DJ .
JOURNAL OF COMPARATIVE NEUROLOGY, 1987, 263 (04) :467-484
[3]   NITRIC-OXIDE SYNTHETASE (NOS)-CONTAINING SYMPATHOADRENAL CHOLINERGIC NEURONS OF THE RAT IML-CELL COLUMN - EVIDENCE FROM HISTOCHEMISTRY, IMMUNOHISTOCHEMISTRY, AND RETROGRADE LABELING [J].
BLOTTNER, D ;
BAUMGARTEN, HG .
JOURNAL OF COMPARATIVE NEUROLOGY, 1992, 316 (01) :45-55
[4]   NITRIC-OXIDE, A NOVEL NEURONAL MESSENGER [J].
BREDT, DS ;
SNYDER, SH .
NEURON, 1992, 8 (01) :3-11
[5]   NITRIC-OXIDE SYNTHASE PROTEIN AND MESSENGER-RNA ARE DISCRETELY LOCALIZED IN NEURONAL POPULATIONS OF THE MAMMALIAN CNS TOGETHER WITH NADPH DIAPHORASE [J].
BREDT, DS ;
GLATT, CE ;
HWANG, PM ;
FOTUHI, M ;
DAWSON, TM ;
SNYDER, SH .
NEURON, 1991, 7 (04) :615-624
[6]   THE NEUROPROTECTIVE EFFECT OF A NITRIC-OXIDE INHIBITOR IN A RAT MODEL OF FOCAL CEREBRAL-ISCHEMIA [J].
BUISSON, A ;
PLOTKINE, M ;
BOULU, RG .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 106 (04) :766-767
[7]  
BUISSON A, 1993, J NEUROCHEM, V61, P690
[8]   NITRIC-OXIDE AND CARDIOVASCULAR CONTROL [J].
CALVER, A ;
COLLIER, J ;
VALLANCE, P .
EXPERIMENTAL PHYSIOLOGY, 1993, 78 (03) :303-326
[9]  
Chen S., 1993, Society for Neuroscience Abstracts, V19, P1876
[10]  
DAWSON VL, 1993, J NEUROSCI, V13, P2651