DIFFERENCES IN D-2 DOPAMINE-RECEPTOR BINDING IN THE NEOSTRIATUM BETWEEN CATS HEMIDECORTICATED NEONATALLY OR IN ADULTHOOD

Citation
Ld. Loopuijt et al., DIFFERENCES IN D-2 DOPAMINE-RECEPTOR BINDING IN THE NEOSTRIATUM BETWEEN CATS HEMIDECORTICATED NEONATALLY OR IN ADULTHOOD, Developmental brain research, 107(1), 1998, pp. 113-122
Citations number
79
Categorie Soggetti
Neurosciences,"Developmental Biology
ISSN journal
01653806
Volume
107
Issue
1
Year of publication
1998
Pages
113 - 122
Database
ISI
SICI code
0165-3806(1998)107:1<113:DIDDBI>2.0.ZU;2-A
Abstract
In order to study differences in response to neocortical injury sustai ned at different ages at the neurotransmitter level, we examined the d ensity in D-2 dopamine receptors in the neostriatum of cats hemidecort icated neonatally (N = 4) or in adulthood (N = 4), as well as in intac t brains (N = 6). Receptor densities were measured using quantitative autoradiography and [H-3]-spiperone binding in 12 regions of the neost riatum and nucleus accumbens septi. We found that the anterior lateral caudate nucleus on both sides of the brain contained a higher D-2 rec eptor density in neonatal-lesioned as compared to adult-lesioned brain s. Ipsilateral to the lesion, the increase was 101% (P < 0.05) and con tralaterally it amounted to 77% (P < 0.05). Moreover, this region of t he ipsilateral caudate nucleus of neonatal-lesioned cats tended to be more densely labeled than that of intact brain by 58% (P < 0.1). D-2 r eceptor densities in adult-lesioned cats did not differ from that of i ntact controls. Comparison of these data with those of a former morpho logical study using the same animals suggested that this bilateral ele vation of D-2 receptor density in neonatally lesioned brains represent s a higher mean density of binding sites per neuron. The elevation in the neonatal-lesioned cats might be a response of the striatum to neur oplastic changes in the striatal neuropil, including the corticostriat al afferents, since such changes are different in neonatal-as compared to adult-lesioned cats. (C) 1998 Elsevier Science B.V.