Age-dependent induction of nitric oxide synthase activity in facial motoneurons after axotomy

被引:23
作者
Mariotti, R [1 ]
Peng, ZC [1 ]
Kristensson, K [1 ]
Bentivoglio, M [1 ]
机构
[1] KAROLINSKA INST,DEPT NEUROSCI,STOCKHOLM,SWEDEN
关键词
D O I
10.1006/exnr.1997.6462
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The facial nerve was transected in rats at different postnatal ages, from birth to early adulthood. NADPH-diaphorase histochemistry was performed to analyze the induction of nitric oxide synthase, the synthetic enzyme of the free radical nitric oxide, in injured facial motoneurons. In addition, in situ nick-end labeling of DNA fragmentation (TUNEL technique) was performed after axotomy at birth, to verify the occurrence of apoptosis in the damaged facial motoneurons. A striking age-dependency was found in the induction of nitric oxide synthase activity in axotomized facial motoneurons. NADPH-diaphorase positivity was not detectable in these neurons 1 and 2 days after axotomy at birth, when apoptotic changes were evident and marked. In addition, NADPH-diaphorase staining was hardly detectable in the facial nucleus 4 days after axotomies at birth, when extensive motoneuron loss was evident. NADPH-diaphorase positivity was instead induced in the facial motoneurons axotomized from the end of the first postnatal week to adulthood, when the nerve cell loss was less severe than in newborns. However, the time course of the enzyme activity induction varied considerably in relation to the animals' age. These findings are discussed in relation to the role of nitric oxide in motoneuron death or protective response to injury and of oxidative stress in neurodegeneration. (C) 1997 Academic Press.
引用
收藏
页码:361 / 370
页数:10
相关论文
共 34 条
[1]  
[Anonymous], ESSAYS NERVOUS SYSTE
[2]   ALDEHYDE FIXATION DIFFERENTIALLY AFFECTS DISTRIBUTION OF DIAPHORASE ACTIVITY BUT NOT OF NITRIC-OXIDE SYNTHASE IMMUNOREACTIVITY IN RAT-BRAIN [J].
BUWALDA, B ;
NYAKAS, C ;
GAST, J ;
LUITEN, PGM ;
SCHMIDT, HHHW .
BRAIN RESEARCH BULLETIN, 1995, 38 (05) :467-473
[3]   AXOTOMY INDUCES NADPH DIAPHORASE ACTIVITY IN NEONATAL BUT NOT ADULT MOTONEURONS [J].
CLOWRY, GJ .
NEUROREPORT, 1993, 5 (03) :361-364
[4]   OXIDATIVE STRESS, GLUTAMATE, AND NEURODEGENERATIVE DISORDERS [J].
COYLE, JT ;
PUTTFARCKEN, P .
SCIENCE, 1993, 262 (5134) :689-695
[5]   DISTRIBUTION OF NADPH-DIAPHORASE REACTIVITY IN THE SPINAL-CORD OF METAMORPHOSING AND ADULT XENOPUS-LAEVIS [J].
CROWE, MJ ;
BROWN, TJ ;
BRESNAHAN, JC ;
BEATTIE, MS .
DEVELOPMENTAL BRAIN RESEARCH, 1995, 86 (1-2) :155-166
[6]  
DAWSON VL, 1993, J NEUROSCI, V13, P2651
[7]   NEONATAL MOTONEURONS OVEREXPRESSING THE BCL-2 PROTOONCOGENE IN TRANSGENIC MICE ARE PROTECTED FROM AXOTOMY-INDUCED CELL-DEATH [J].
DUBOISDAUPHIN, M ;
FRANKOWSKI, H ;
TSUJIMOTO, Y ;
HUARTE, J ;
MARTINOU, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3309-3313
[8]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[9]   DELAYED ASTROCYTE REACTION FOLLOWING FACIAL-NERVE AXOTOMY [J].
GRAEBER, MB ;
KREUTZBERG, GW .
JOURNAL OF NEUROCYTOLOGY, 1988, 17 (02) :209-220
[10]   SUPEROXIDE-DISMUTASE DELAYS NEURONAL APOPTOSIS - A ROLE FOR REACTIVE OXYGEN SPECIES IN PROGRAMMED NEURONAL DEATH [J].
GREENLUND, LJS ;
DECKWERTH, TL ;
JOHNSON, EM .
NEURON, 1995, 14 (02) :303-315