Literature DB >> 1977408

Behavioural and neurochemical effects of Ro 40-7592, a new COMT inhibitor with a potential therapeutic activity in Parkinson's disease.

J Maj1, Z Rogóz, G Skuza, H Sowińska, J Superata.   

Abstract

Behavioural and some neurochemical effects of Ro 40-7592 (3,4-dihydroxy-4'-methyl-5-nitrobenzophenone), a new COMT inhibitor, were studied in rats and mice. Ro 40-7592 increased the effect of L-DOPA (plus benserazide) on locomotor activity, reserpine-induced hypothermia, and catalepsy induced by pimozide, haloperidol and fluphenazine. Locomotor hyperactivity induced by amphetamine or nomifensine, as well as stereotypy induced by amphetamine (but not apomorphine), were also increased by Ro 40-7592. The drug stimulated exploratory activity in the open field test. It decreased the levels of HVA and 3-MT, increased the level of DOPAC but did not change the levels of dopamine in the striatum, nucleus accumbens and frontal cortex. These results indicate that Ro 40-7592 may improve the therapy with L-DOPA (plus decarboxylase inhibitor) of Parkinson's disease.

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Year:  1990        PMID: 1977408     DOI: 10.1007/bf02260898

Source DB:  PubMed          Journal:  J Neural Transm Park Dis Dement Sect        ISSN: 0936-3076


  12 in total

1.  Effect of monoamine oxidase A and B and of catechol-O-methyltransferase inhibition on L-DOPA-induced circling behavior.

Authors:  M J Heeringa; F d'Agostini; P DeBoer; M DaPrada; G Damsma
Journal:  J Neural Transm (Vienna)       Date:  1997       Impact factor: 3.575

2.  In vivo effects of new inhibitors of catechol-O-methyl transferase.

Authors:  E Rivas; M L de Ceballos; O Nieto; J A Fontenla
Journal:  Br J Pharmacol       Date:  1999-04       Impact factor: 8.739

3.  Peripheral and central inhibitors of catechol-O-methyl transferase: effects on liver and brain COMT activity and L-DOPA metabolism.

Authors:  T Brannan; A Prikhojan; M D Yahr
Journal:  J Neural Transm (Vienna)       Date:  1997       Impact factor: 3.575

4.  Biochemical and pharmacological properties of a peripherally acting catechol-O-methyltransferase inhibitor entacapone.

Authors:  E Nissinen; I B Lindén; E Schultz; P Pohto
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1992-09       Impact factor: 3.000

5.  Synergistic interactions between COMT-/MAO-inhibitors and L-Dopa in MPTP-treated mice.

Authors:  A Fredriksson; T Archer
Journal:  J Neural Transm Gen Sect       Date:  1995

6.  Comparison of two new inhibitors of catechol O-methylation on striatal dopamine metabolism: a microdialysis study in rats.

Authors:  M Törnwall; S Kaakkola; P Tuomainen; A Kask; P T Männistö
Journal:  Br J Pharmacol       Date:  1994-05       Impact factor: 8.739

7.  The COMT inhibitor tolcapone potentiates the anticataleptic effect of Madopar in MPP(+)-lesioned mice.

Authors:  N Himori; K Mishima
Journal:  Experientia       Date:  1994-10-15

Review 8.  Animal models of Parkinson's disease: a source of novel treatments and clues to the cause of the disease.

Authors:  Susan Duty; Peter Jenner
Journal:  Br J Pharmacol       Date:  2011-10       Impact factor: 8.739

9.  Variability in Dopamine Genes Dissociates Model-Based and Model-Free Reinforcement Learning.

Authors:  Bradley B Doll; Kevin G Bath; Nathaniel D Daw; Michael J Frank
Journal:  J Neurosci       Date:  2016-01-27       Impact factor: 6.167

10.  Sexually dimorphic effects of catechol-O-methyltransferase (COMT) inhibition on dopamine metabolism in multiple brain regions.

Authors:  Linda M Laatikainen; Trevor Sharp; Paul J Harrison; Elizabeth M Tunbridge
Journal:  PLoS One       Date:  2013-04-16       Impact factor: 3.240

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