INDUCTION OF MICROGLIAL REACTION AND EXPRESSION OF NITRIC-OXIDE SYNTHASE-I IN THE NUCLEUS DORSALIS AND RED NUCLEUS FOLLOWING LOWER THORACICSPINAL-CORD HEMISECTION
M. Xu et al., INDUCTION OF MICROGLIAL REACTION AND EXPRESSION OF NITRIC-OXIDE SYNTHASE-I IN THE NUCLEUS DORSALIS AND RED NUCLEUS FOLLOWING LOWER THORACICSPINAL-CORD HEMISECTION, Brain research, 808(1), 1998, pp. 23-30
In the present study, immunohistochemical stainings for OX-6, OX-42, n
itric oxide synthase I and II as well as nitrotyrosine were used to in
vestigate possible correlation among microglial reactivity, nitric oxi
de synthase upregulation, peroxynitrite involvement and neuronal death
in the nucleus dorsalis and red nucleus following lower thoracic spin
al cord hemisection. Significant neuronal loss was found in the ipsila
teral nucleus dorsalis and contralateral red nucleus after cord hemise
ction. A distinctive microglial reaction for OX-42 could be observed f
rom one to four weeks post axotomy in the ipsilateral nucleus dorsalis
; by contrast, it was observed on both sides of the red nucleus from o
ne to three weeks following cord hemisection. The activated microglial
cells showed some degree of hypertrophy. From the microglial immunore
activity as well as their appearance, it was speculated that microglia
l activation might be beneficial or protective to the axotomized neuro
ns. In normal and sham-operated rats, neurons of the nucleus dorsalis
were not nitric oxide synthase I reactive. Three weeks after cord hemi
section, neurons in the ipsilateral nucleus dorsalis below the lesion
showed strong immunoreactivity. Neurons in the red nucleus that normal
ly displayed weak nitric oxide synthase I immunoreactivity showed an i
ncrease on both sides of the nucleus. These results suggested that nit
ric oxide synthase I expression in the nucleus dorsalis following axot
omy was synthesized de novo and might act as a neurotoxic agent. Howev
er, the bilateral increase in expression of nitric oxide synthase I in
the red nucleus after lower thoracic cord hemisection was due to up-r
egulation of the constitutive enzyme and might have some neuroprotecti
ve function. Our results also suggested that peroxynitrite played no o
r little role in the neurodegeneration in the nucleus dorsalis and red
nucleus following axotomy. (C) 1998 Elsevier Science B.V. All rights
reserved.