Literature DB >> 1970757

Tyrosine hydroxylase and cholecystokinin mRNA levels in the substantia nigra, ventral tegmental area, and locus ceruleus are unaffected by acute and chronic haloperidol administration.

S L Cottingham1, D Pickar, T K Shimotake, P Montpied, S M Paul, J N Crawley.   

Abstract

1. The studies described herein were designed to test the hypothesis that a neuroleptic, haloperidol, may alter the level of expression of the tyrosine hydroxylase and cholecystokinin genes in discrete brain regions. 2. In situ hybridization was employed to quantitate changes in concentration of mRNA for tyrosine hydroxylase and cholecystokinin in the ventral tegmental area, substantia nigra, and locus ceruleus after acute or chronic treatment with haloperidol or vehicle. 3. Haloperidol had no effect on the level of tyrosine hydroxylase or cholecystokinin mRNAs, in the ventral tegmentum, substantia nigra, or locus ceruleus, at either 3 or 19 days of drug administration. 4. These data suggest that haloperidol administration does not alter the level of tyrosine hydroxylase or cholecystokinin mRNAs in midbrain dopamine neurons of the rat.

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Year:  1990        PMID: 1970757     DOI: 10.1007/bf00733634

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  31 in total

Review 1.  Perspectives on a time-dependent model of neuroleptic action.

Authors:  D Pickar
Journal:  Schizophr Bull       Date:  1988       Impact factor: 9.306

2.  ATP, cyclic AMP, and magnesium increase the affinity of rat striatal tyrosine hydroxylase for its cofactor.

Authors:  W Lovenberg; E A Bruckwick; I Hanbauer
Journal:  Proc Natl Acad Sci U S A       Date:  1975-08       Impact factor: 11.205

3.  Direct phosphorylation of brain tyrosine hydroxylase by cyclic AMP-dependent protein kinase: mechanism of enzyme activation.

Authors:  T H Joh; D H Park; D J Reis
Journal:  Proc Natl Acad Sci U S A       Date:  1978-10       Impact factor: 11.205

4.  Regional sensitivity of primate brain dopaminergic neurons to haloperidol: alterations following chronic treatment.

Authors:  N G Bacopoulos; G Bustos; D E Redmond; J Baulu; R H Roth
Journal:  Brain Res       Date:  1978-11-24       Impact factor: 3.252

5.  Peptide-monoamine coexistence: studies of the actions of cholecystokinin-like peptide on the electrical activity of midbrain dopamine neurons.

Authors:  L R Skirboll; A A Grace; D W Hommer; J Rehfeld; M Goldstein; T Hökfelt; B S Bunney
Journal:  Neuroscience       Date:  1981       Impact factor: 3.590

6.  Complete coding sequence of rat tyrosine hydroxylase mRNA.

Authors:  B Grima; A Lamouroux; F Blanot; N F Biguet; J Mallet
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

7.  A subpopulation of mesencephalic dopamine neurons projecting to limbic areas contains a cholecystokinin-like peptide: evidence from immunohistochemistry combined with retrograde tracing.

Authors:  T Hökfelt; L Skirboll; J F Rehfeld; M Goldstein; K Markey; O Dann
Journal:  Neuroscience       Date:  1980       Impact factor: 3.590

8.  Haloperidol: effect of long-term treatment on rat striatal dopamine synthesis and turnover.

Authors:  P Lerner; P Nosé; E K Gordon; W Lovenberg
Journal:  Science       Date:  1977-07-08       Impact factor: 47.728

9.  Regional localization of the mRNA coding for the neuropeptide cholecystokinin in the rat brain studied by in situ hybridization.

Authors:  M Savasta; J M Palacios; G Mengod
Journal:  Neurosci Lett       Date:  1988-11-11       Impact factor: 3.046

10.  In vivo electrochemical analysis of cholecystokinin-induced inhibition of dopamine release in the nucleus accumbens.

Authors:  R F Lane; C D Blaha; A G Phillips
Journal:  Brain Res       Date:  1986-11-05       Impact factor: 3.252

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  1 in total

1.  Regulation of tyrosine hydroxylase expression in tottering mouse Purkinje cells.

Authors:  Brandy E Fureman; Daniel B Campbell; Ellen J Hess
Journal:  Neurotox Res       Date:  2003       Impact factor: 3.911

  1 in total

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