Kainic acid decreases hippocampal neuronal number and increases dopamine receptor binding in the nucleus accumbens: an animal model of schizophrenia. Behav Brain Res 1995 Oct;70(2):153-64
Date
10/01/1995Pubmed ID
8561906DOI
10.1016/0166-4328(95)80005-0Scopus ID
2-s2.0-0028858579 (requires institutional sign-in at Scopus site) 43 CitationsAbstract
Intracerebroventricular (i.c.v.) administration of kainic acid (KA) produces graded neuronal loss in the hippocampus and other regions of the medial temporal lobe. Many of these brain regions send excitatory projections to the nucleus accumbens, a dopaminergic brain area implicated in psychotomimetic and antipsychotic drug action. In the present study, neurochemical function in the nucleus accumbens and anterior caudate-putamen was examined one week after i.c.v. administration of 1.5, 4.5, or 6.6 nmol of KA. As expected, i.c.v. KA produced dose-dependent neuronal loss in the dorsal and ventral hippocampus. Extrahippocampal neuronal loss was also observed in the thalamus and piriform cortex in some of the KA-treated rats. While ambient levels of dopamine turnover and excitatory amino acids in the nucleus accumbens were unaltered by KA, administration of the highest KA dose elevated [3H]spiperone binding exclusively in the accumbens. Finally, behavioral hyperactivity was observed in KA-treated rats over a five-week period following i.c.v. administration. The pattern of neuronal loss, receptor upregulation, and behavioral hyperactivity found after i.c.v. KA administration may provide a useful animal model of the limbic neuropathology and neurochemical dysfunction associated with schizophrenia.
Author List
Bardgett ME, Jackson JL, Taylor GT, Csernansky JGAuthor
Jeffrey L. Jackson MD Professor in the Medicine department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
AnimalsBrain Mapping
Caudate Nucleus
Cell Count
Disease Models, Animal
Dose-Response Relationship, Drug
Hippocampus
Injections, Intraventricular
Kainic Acid
Male
Motor Activity
Nerve Degeneration
Neural Pathways
Nucleus Accumbens
Putamen
Rats
Rats, Sprague-Dawley
Receptors, Dopamine
Schizophrenia
Spiperone
Temporal Lobe
Up-Regulation
