Literature DB >> 3161742

Influence of renal failure on the kinetics of zimeldine and norzimelidine.

N Ferry, G Cuisinaud, P Cochat, N Pozet, P Y Zech, J Sassard.   

Abstract

The kinetics of zimeldine (Z) and its demethylated metabolite, norzimelidine (NZ), were determined after administration of a single 200 mg oral dose of Z to 6 healthy volunteers (Group I), and to patients with mild (Group II) and severe renal failure (Group III). Z and NZ concentrations were assayed by HPLC in serial plasma and urine samples over 6 days following the dose. In Group I Z was rapidly absorbed and metabolized into NZ, and then the plasma concentrations declined with apparent elimination half-lives of 8.4 h and 24.9 h for Z and NZ respectively, whilst the renal clearance of both compounds was low, Z 15.7 ml/min and NZ 33.0 ml/min. The plasma level of Z differed little between Groups I and III, but the area under the curve was significantly higher in Group III than in Group I subjects (AUC0-144 = 17.3 and 6.8 mumol X l-1 X h, respectively). Severe renal failure did not affect the peak plasma concentration of NZ but it did significantly increase peak time, apparent elimination half-life, and the area under the plasma concentration curve. A significant inverse relationship was found between renal clearance of NZ and plasma creatinine. Since NZ is as pharmacologically potent as Z, the results suggest that the dose of Z should be reduced in patients with severe renal insufficiency.

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Year:  1985        PMID: 3161742     DOI: 10.1007/bf00544366

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  7 in total

1.  Pharmacokinetics of zimelidine. Systemic availability of zimelidine and norzimelidine in human volunteers.

Authors:  D Brown; D H Scott; D B Scott; M Meyer; D Westerlund; J Lundström
Journal:  Eur J Clin Pharmacol       Date:  1980-02       Impact factor: 2.953

2.  Zimelidine: a therapeutic and pharmacokinetic study in depression.

Authors:  A Coppen; V A Ramo Rao; C Swade; K Wood
Journal:  Psychopharmacology (Berl)       Date:  1979-06-21       Impact factor: 4.530

3.  Reversed-phase chromatography of zimelidine and similar dibasic amines. I. Analysis in biological material.

Authors:  D Westerlund; E Erixson
Journal:  J Chromatogr       Date:  1979-12-20

4.  Initial clinical trial based on biochemical methodology of zimelidine (a serotonin uptake inhibitor) in depressed patients.

Authors:  B Siwers; V A Ringberger; J R Tuck; F Sjöqvist
Journal:  Clin Pharmacol Ther       Date:  1977-02       Impact factor: 6.875

5.  Pharmacokinetic study of zimelidine using a new GLC method.

Authors:  G Caillé; E Kouassi; C de Montigny
Journal:  Clin Pharmacokinet       Date:  1983 Nov-Dec       Impact factor: 6.447

6.  A double-blind study of zimelidine, a serotonin uptake inhibitor, and desipramine, a noradrenaline uptake inhibitor, in endogenous depression. II. Biochemical findings.

Authors:  A Aberg-Wistedt; S B Ross; K G Jostell; B Sjöquist
Journal:  Acta Psychiatr Scand       Date:  1982-07       Impact factor: 6.392

7.  Controlled cross-over study of a 5-HT uptake inhibiting and an NA uptake inhibiting antidepressant.

Authors:  A Aberg
Journal:  Acta Psychiatr Scand Suppl       Date:  1981
  7 in total

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