Coordinate suppression of striatal ngfi-a and c-fos produces locomotor asymmetry and up-regulation of IEGs in the globus pallidus

M. O. Hebb, H. A. Robertson

Research output: Contribution to journalArticlepeer-review

18 Citations (Scopus)

Abstract

We have studied the effects of inhibition of c-Fos and NGFI-A expression by intrastriatal infusion of end-capped antisense oligodeoxynucleotides to determine if their coordinate expression is conferred independently or through regulatory influences exerted between these two proteins. The previously reported locomotor bias that has been associated with unilateral c-Fos suppression was also investigated in animals receiving antisense oligodeoxynucleotides targeted to ngfi-a to determine if the behavior is specific to alterations in c-Fos expression, or if its cause may be a generalized imbalance of striatal IEGs. We show here that while unilateral suppression of c-Fos has negligible effects on NGFI-A, oligodeoxynucleotides targeted to ngfi-a markedly inhibit both NGFI-A and c-Fos expression. Animals with extensive unilateral reduction of either or both proteins demonstrated robust ipsiversive rotation when challenged with D-amphetamine. Infusions of random oligodeoxynucleotides produced neither a reduction in c-Fos or NGFI-A expression, nor a significant rotational bias following D-amphetamine challenge. Surprisingly, animals with extensive striatal IEG suppression were found to have marked up-regulation of c-Fos and NGFI-A in the ipsilateral globus pallidus, a finding which may ultimately shed light on the mechanism of antisense-induced rotational behavior.

Original languageEnglish
Pages (from-to)97-106
Number of pages10
JournalMolecular Brain Research
Volume48
Issue number1
DOIs
Publication statusPublished - Aug 1997

Bibliographical note

Funding Information:
We would like to thank K. Murphy, B. Ross and M. Peterson for excellent technical support as well as Drs. M. Hong, J. Armstrong and J. Babity for their advice and constructive criticism. This work was supported by the MRC and SmithKline Beecham. M.O.H. is supported by a studentship from the Huntington Society of Canada.

ASJC Scopus Subject Areas

  • Molecular Biology
  • Cellular and Molecular Neuroscience

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