Matches in SemOpenAlex for { <https://semopenalex.org/work/W2041805766> ?p ?o ?g. }
- W2041805766 endingPage "174" @default.
- W2041805766 startingPage "167" @default.
- W2041805766 abstract "The present study was carried out to test whether the abnormally high striatal Fos activation induced by amphetamine and the overcompensation of amphetamine-induced rotation in 6-hydroxydopamine-lesioned rats receiving transplants of fetal nigral neurons can be reduced by a lesion of the corticostriatal projection. Fetal ventral mesencephalic tissue was transplanted as a cell suspension into the dopamine-denervated striatum of unilaterally 6-hydroxydopamine-lesioned rats. Rats in which the transplants had produced a complete compensation or reversal of the lesion-induced rotational asymmetry in response to amphetamine (5 mg/kg, i.p.) were divided into two equal groups, sustaining either a knife-cut transection of prefrontal corticofugal efferents ipsilaterally to the grafts, or a sham-lesion. The animals were re-tested for amphetamine-induced rotation one week post-operatively, and were perfusion-fixed two hours after drug administration. Adjacent sections through the striatum were processed for Fos and tyrosine hydroxylase immunohistochemistry. At the amphetamine rotation test performed after cortical lesion surgery, the frontocortically deafferented animals exhibited a low rate of rotation in the direction ipsilateral to the dopaminergically denervated and grafted side, while sham-lesioned rats rotated towards the intact side. In sham-lesioned controls, the density of Fos-immunoreactive nuclei (no. of nuclei/mm2) was significantly higher in the reinnervated portion of the grafted striatum than on the contralateral side (+54 to 316%). In the frontocortically deafferented-grafted striata, Fos expression was not different from that measured on the contralateral side and significantly lower than in the sham-lesioned controls (−65–79%). The frontocortical transection reduced the density of Fos-positive nuclei also in the ipsilateral globus pallidus (−52% in transected vs. sham-lesioned group). The present data suggest that the hyperexpression of Fos induced by amphetamine in the reinnervated portion of the grafted striatum, as well as the development of overcompensation of amphetamine-induced turning, are dependent on abnormal functional interactions between the innate corticostriatal input and the new dopaminergic innervation provided by the transplanted nigral neurons." @default.
- W2041805766 created "2016-06-24" @default.
- W2041805766 creator A5032191531 @default.
- W2041805766 creator A5047762447 @default.
- W2041805766 date "1994-11-01" @default.
- W2041805766 modified "2023-09-27" @default.
- W2041805766 title "Transection of corticostriatal afferents abolishes the hyperexpression of Fos and counteracts the development of rotational overcompensation induced by intrastriatal dopamine-rich grafts when challenged with amphetamine" @default.
- W2041805766 cites W1593383161 @default.
- W2041805766 cites W1626273676 @default.
- W2041805766 cites W1798056883 @default.
- W2041805766 cites W1884206649 @default.
- W2041805766 cites W1964108939 @default.
- W2041805766 cites W1968722941 @default.
- W2041805766 cites W1970979709 @default.
- W2041805766 cites W1971073326 @default.
- W2041805766 cites W1971465507 @default.
- W2041805766 cites W1979058276 @default.
- W2041805766 cites W1980272233 @default.
- W2041805766 cites W1982386259 @default.
- W2041805766 cites W2004757843 @default.
- W2041805766 cites W2005487930 @default.
- W2041805766 cites W2008631499 @default.
- W2041805766 cites W2021365267 @default.
- W2041805766 cites W2022726524 @default.
- W2041805766 cites W2026306356 @default.
- W2041805766 cites W2027724821 @default.
- W2041805766 cites W2028247815 @default.
- W2041805766 cites W2032551004 @default.
- W2041805766 cites W2041487100 @default.
- W2041805766 cites W2060211846 @default.
- W2041805766 cites W2062524799 @default.
- W2041805766 cites W2066113689 @default.
- W2041805766 cites W2071656982 @default.
- W2041805766 cites W2087249096 @default.
- W2041805766 cites W2111840943 @default.
- W2041805766 doi "https://doi.org/10.1016/0006-8993(94)91170-3" @default.
- W2041805766 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/7882012" @default.
- W2041805766 hasPublicationYear "1994" @default.
- W2041805766 type Work @default.
- W2041805766 sameAs 2041805766 @default.
- W2041805766 citedByCount "28" @default.
- W2041805766 countsByYear W20418057662013 @default.
- W2041805766 crossrefType "journal-article" @default.
- W2041805766 hasAuthorship W2041805766A5032191531 @default.
- W2041805766 hasAuthorship W2041805766A5047762447 @default.
- W2041805766 hasConcept C105702510 @default.
- W2041805766 hasConcept C126322002 @default.
- W2041805766 hasConcept C134018914 @default.
- W2041805766 hasConcept C137183658 @default.
- W2041805766 hasConcept C142724271 @default.
- W2041805766 hasConcept C159167319 @default.
- W2041805766 hasConcept C169760540 @default.
- W2041805766 hasConcept C185592680 @default.
- W2041805766 hasConcept C2776355744 @default.
- W2041805766 hasConcept C2776805190 @default.
- W2041805766 hasConcept C2777193897 @default.
- W2041805766 hasConcept C2777288102 @default.
- W2041805766 hasConcept C2778187257 @default.
- W2041805766 hasConcept C2780062018 @default.
- W2041805766 hasConcept C2780938664 @default.
- W2041805766 hasConcept C2781156865 @default.
- W2041805766 hasConcept C2911016594 @default.
- W2041805766 hasConcept C513476851 @default.
- W2041805766 hasConcept C529278444 @default.
- W2041805766 hasConcept C71924100 @default.
- W2041805766 hasConcept C86803240 @default.
- W2041805766 hasConceptScore W2041805766C105702510 @default.
- W2041805766 hasConceptScore W2041805766C126322002 @default.
- W2041805766 hasConceptScore W2041805766C134018914 @default.
- W2041805766 hasConceptScore W2041805766C137183658 @default.
- W2041805766 hasConceptScore W2041805766C142724271 @default.
- W2041805766 hasConceptScore W2041805766C159167319 @default.
- W2041805766 hasConceptScore W2041805766C169760540 @default.
- W2041805766 hasConceptScore W2041805766C185592680 @default.
- W2041805766 hasConceptScore W2041805766C2776355744 @default.
- W2041805766 hasConceptScore W2041805766C2776805190 @default.
- W2041805766 hasConceptScore W2041805766C2777193897 @default.
- W2041805766 hasConceptScore W2041805766C2777288102 @default.
- W2041805766 hasConceptScore W2041805766C2778187257 @default.
- W2041805766 hasConceptScore W2041805766C2780062018 @default.
- W2041805766 hasConceptScore W2041805766C2780938664 @default.
- W2041805766 hasConceptScore W2041805766C2781156865 @default.
- W2041805766 hasConceptScore W2041805766C2911016594 @default.
- W2041805766 hasConceptScore W2041805766C513476851 @default.
- W2041805766 hasConceptScore W2041805766C529278444 @default.
- W2041805766 hasConceptScore W2041805766C71924100 @default.
- W2041805766 hasConceptScore W2041805766C86803240 @default.
- W2041805766 hasIssue "1" @default.
- W2041805766 hasLocation W20418057661 @default.
- W2041805766 hasLocation W20418057662 @default.
- W2041805766 hasOpenAccess W2041805766 @default.
- W2041805766 hasPrimaryLocation W20418057661 @default.
- W2041805766 hasRelatedWork W1973027408 @default.
- W2041805766 hasRelatedWork W1987055095 @default.
- W2041805766 hasRelatedWork W2001882521 @default.
- W2041805766 hasRelatedWork W2011277388 @default.
- W2041805766 hasRelatedWork W2019842877 @default.
- W2041805766 hasRelatedWork W2030616263 @default.