Full Record Display for the EPA National Library Catalog

RECORD NUMBER: 615 OF 886

Main Title Neurotoxicity of Acrylamide and 2,5-Hexanedione in Rats Evaluated Using a Functional Observational Battery and Pathological Examination.
Author Shell, L. ; Rozum, M. ; Jortner, B. S. ; Ehrich, M. ;
CORP Author Virginia-Maryland Regional Coll. of Veterinary Medicine, Blacksburg, VA. ;Virginia Polytechnic Inst. and State Univ., Blacksburg. Dept. of Statistics.;Health Effects Research Lab., Research Triangle Park, NC.
Publisher c1992
Year Published 1992
Report Number EPA-68D80098; EPA/600/J-94/396;
Stock Number PB95-126488
Additional Subjects Acrylamides ; Nervous system ; Pathology ; Toxicity ; Esterases ; Dose-response relationships ; Reprints ; Functional observational battery ; Hexanediones
Holdings
Library Call Number Additional Info Location Last
Modified
Checkout
Status
NTIS  PB95-126488 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 14p
Abstract The clinical effects of two neurotoxicants, acrylamide and 2,5-hexanedione, were compared in rats using a functional observational battery (FOB), which includes a series of home cage and open-field observations, sensorimotor measurements, and physiological parameters. Neurotoxicity was assessed weekly in adult male Long-Evans rats after initiation of IP administration of 9 doses of acrylamide (12, 15, or 50 mg/kg given 3 times a week) and 28 doses of 2,5-hexanedione (150, 225, and 350 mg/kg given daily). Using the FOB, it was possible to detect differences in neurotoxic effects of these two chemicals. Acrylamide significanly affected home cage posture, foot splay and time on the rotarod, whereas 2,5-hexanedione altered hindlimb grip strength and the approach response. Both compounds caused changes in ability to walk, right, and maintain agility on a rotarod within 21 days from initiation of toxicant administration. In addition, both compounds caused dose-dependent rats and at 28 days in rats treated with 2,5-hexanedione. Administration of acrylamide also decreased activities of neural esterase. The study indicated that the FOB could be used to detect evidence of neurotoxicity in rats treated with acrylamide and 2,5-hexanedione, with alterations evident even before pathological changes were induced by 2,5-hexanedione. (Copyright (c) 1992 Pergamon Press Ltd.)
Supplementary Notes Pub. in Neurotoxicology and Teratology, v14 n4 p273-283 1992. See also PB92-113323. Prepared in cooperation with Virginia Polytechnic Inst. and State Univ., Blacksburg. Dept. of Statistics. Sponsored by Health Effects Research Lab., Research Triangle Park, NC.
NTIS Title Notes Journal article.
Title Annotations Reprint: Neurotoxicity of Acrylamide and 2,5-Hexanedione in Rats Evaluated Using a Functional Observational Battery and Pathological Examination.
Category Codes 57Y; 57S; 57O
NTIS Prices PC A03/MF A01
Primary Description 600/10
Document Type NT
Cataloging Source NTIS/MT
Control Number 433519187
Origin NTIS
Type CAT