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RECORD NUMBER: 18 OF 244

OLS Field Name OLS Field Data
Main Title Administration of 3,3'-Iminodipropionitrile to the Rat Results in Region-Dependent Damage to the Central Nervous System at Levels Above the Brain Stem.
Author Llorens, J. ; Crofton, K. M. ; O'Callaghan, J. P. ;
CORP Author Health Effects Research Lab., Research Triangle Park, NC. Neurotoxicology Div.
Publisher 1993
Year Published 1993
Report Number EPA/600/J-94/025;
Stock Number PB94-137296
Additional Subjects Central nervous system ; Toxicity ; Prefrontal cortex ; Rats ; Glial fibrillary acidic protein ; Body weight ; Cerebral cortex ; Olfactory bulb ; Reprints ; Nitrile/iminodipropio
Holdings
Library Call Number Additional Info Location Last
Modified
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Status
NTIS  PB94-137296 Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy. NTIS 05/14/1994
Collation 9p
Abstract
The neurotoxicant 3,3'-iminodipropionitrile (IDPN) induces a persistent neurological syndrome and an axonopathic condition. In this study, the concentration of glial fibrillary acidic protein (GFAP), measured by solid-phase radioimmunoassay in brain tissue homogenates, was used as a marker of the reactive gliosis occurring in the central nervous system after IDPN intoxication. Male Long-Evans rats were given 3 daily i.p. injections of 0-600 mg/kg/day of IDPN in saline. Seven days after 3 X 400 mg/kg/day, GFAP increases were observed in pons-medulla, midbrain, olfactory bulbs and cerebral cortex, but not in cerebellum, hypothalamus, hippocampus and striatum. Dose-dependent increases in GFAP were observed in the cortex at 10 days after administration, whereas no GFAP response was observed in the cerebellum of the same animals. GFAP increases were obtained in either cingulate, frontal, parietal and occipital-temporal cortical areas 10 days after 3 X 400 mg/kg/day. A large effect was also observed in olfactory bulbs at the same dose and time. The effect of the 3 X 400 mg/kg/day treatment on cingulate cortex GFAP was observed to have a rapid onset, with a peak around one week, and a recovery to basal levels within two weeks after administration. The present results demonstrate region specific, dose- and time-dependent increases in GFAP in the CNS of rats exposed to IDPN.