Literature DB >> 3998771

Three-year observation of mesulergine (CU 32-085) in advanced and newly treated parkinsonism.

E Schneider, H Baas, P A Fischer, G Japp.   

Abstract

In 15 patients (8 men, 7 women), aged 44-81 years, with idiopathic parkinsonism, the effects of mesulergine (CU 32-085) were observed for up to 3 years. Of these patients, four had been without previous levodopa treatment, five had been on levodopa/decarboxylase inhibitor for 6.4 years and six patients had been on levodopa/decarboxylase inhibitor and bromocriptine for a period of 7.5 years. Mesulergine proved to be effective in all three groups of patients and for each main symptom of the disease. Rigidity and tremor showed a better response than akinesia. A decline in efficacy could be observed after 18 months of treatment. By increasing the levodopa dosage, the worsening of the symptomatology could be reduced again and after 3 years patients were slightly better off than before the introduction of mesulergine. Fine motor performance showed a longer-lasting improvement than walking, which was affected by an increase of freezing. Mesulergine was not fully sufficient when given in monotherapy and the levodopa saving effect was only temporary. Parallel with the decline in the therapeutic response as assessed by the rating scales, there was a worsening in the on/off symptomatology. The on/off symptoms, evaluated by patients themselves, had shown very small or no improvement at the beginning of mesulergine administration, contrasting with the findings reflected in the assessment scales. The most frequent side-effects were hallucinations and dyskinesias. Orthostatic hypotension did not prove a problem. Dyskinesias were not seen during monotherapy with mesulergine in de novo patients.

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Year:  1985        PMID: 3998771     DOI: 10.1007/bf00314036

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  15 in total

1.  [Influence of L-DOPA on night sleep in parkinsonian patients].

Authors:  K Kendel; U Beck; C Wita; E Hohneck; H Zimmermann
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1972

2.  Should dopamine agonists be given early or late in the treatment of Parkinson's disease?

Authors:  A Rascol; J L Montastruc; O Rascol
Journal:  Can J Neurol Sci       Date:  1984-02       Impact factor: 2.104

3.  Therapeutic experience with the new dopamine agonist CU 32-085 in advanced Parkinson's disease.

Authors:  H Biesemeyer; H P Ludin; E Ringwald
Journal:  J Neurol       Date:  1983       Impact factor: 4.849

4.  Treatment of Parkinson's disease with 8-alpha-amino-ergoline, CU 32-085.

Authors:  E Schneider; K Hubener; P A Fischer
Journal:  Neurology       Date:  1983-04       Impact factor: 9.910

5.  Mesulergine and its 1,20-N,N-bidemethylated metabolite interact directly with D1- and D2-receptors.

Authors:  R Markstein
Journal:  Eur J Pharmacol       Date:  1983-11-11       Impact factor: 4.432

6.  Should dopamine agonists be given early or late? A review of nine years experience with bromocriptine.

Authors:  A N Lieberman; G Gopinathan; H Hassouri; A Neophytides; M Goldstein
Journal:  Can J Neurol Sci       Date:  1984-02       Impact factor: 2.104

7.  Long-term efficacy of bromocriptine in Parkinson disease.

Authors:  A Lieberman; M Kupersmith; A Neophytides; I Casson; R Durso; S H Foo; M Khayali; G Bear; M Goldstein
Journal:  Neurology       Date:  1980-05       Impact factor: 9.910

8.  Two novel prolactin release-inhibiting 8 alpha-amino-ergolines.

Authors:  E Flückiger; U Briner; H R Bürki; P Marbach; H R Wagner; W Doepfner
Journal:  Experientia       Date:  1979-12-15

9.  Dopaminergic properties of mesulergine (CU 32-085) and its metabolites.

Authors:  A Enz; P Donatsch; R Nordmann
Journal:  J Neural Transm       Date:  1984       Impact factor: 3.575

10.  Adjuvant treatment of Parkinson's disease with dopamine agonists: open trial with bromocriptine and CU 32-085.

Authors:  K Jellinger
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

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