Literature DB >> 8149947

Steady state investigation of possible pharmacokinetic interactions of moxonidine and glibenclamide.

M Müller1, H J Weimann, G Eden, W Weber, K Michaelis, C Dilger, G Achtert.   

Abstract

The aim of the study presented here was to determine possible pharmacokinetic interactions of moxonidine and glibenclamide at steady state in 18 healthy male volunteers. Multiple oral doses of 0.2 mg of moxonidine b.i.d. (q. 12 h) and of 2.5 mg of glibenclamide o.i.d. (q. 24 h) were administered alone and in combination in an open, non-randomized, three-treatment design. The preparations were given for 5 days in each of the 3 periods. The results of this multiple dose study did not indicate substantial pharmacokinetic interactions of the drugs. Regarding the influence of glibenclamide on the pharmacokinetics of moxonidine, no significant changes were seen at all. In the presence of moxonidine, a minor decrease of bioavailability of glibenclamide was detectable, as could be derived from the AUC and clearance data. The actual differences were small and not considered to be of clinical significance.

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Year:  1993        PMID: 8149947     DOI: 10.1007/BF03188809

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  7 in total

1.  Evidence for the existence of a homogeneous population of imidazoline receptors in the human brainstem.

Authors:  G Bricca; M Dontenwill; A Molines; J Feldman; A Belcourt; P Bousquet
Journal:  Eur J Pharmacol       Date:  1988-06-10       Impact factor: 4.432

2.  Pharmacokinetics of moxonidine after single and repeated daily doses in healthy volunteers.

Authors:  D Trenk; F Wagner; E Jähnchen; V Plänitz
Journal:  J Clin Pharmacol       Date:  1987-12       Impact factor: 3.126

3.  The influence of renal function on clinical pharmacokinetics of moxonidine.

Authors:  W Kirch; H J Hutt; V Plänitz
Journal:  Clin Pharmacokinet       Date:  1988-10       Impact factor: 6.447

4.  Role of imidazole receptors in the vasodepressor response to clonidine analogs in the rostral ventrolateral medulla.

Authors:  P Ernsberger; R Giuliano; R N Willette; D J Reis
Journal:  J Pharmacol Exp Ther       Date:  1990-04       Impact factor: 4.030

5.  Unique presynaptic alpha 2-receptor selectivity and specificity of the antihypertensive agent moxonidine.

Authors:  B I Armah
Journal:  Arzneimittelforschung       Date:  1988-10

6.  Absolute bioavailability of moxonidine.

Authors:  R Theodor; H J Weimann; W Weber; K Michaelis
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1991 Apr-Jun       Impact factor: 2.441

7.  Crossover comparison of moxonidine and clonidine in mild to moderate hypertension.

Authors:  V Plänitz
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

  7 in total
  2 in total

1.  Quinidine does not affect the renal clearance of moxonidine.

Authors:  Stephen D Wise; Clark Chan; Hans G Schaefer; Minxia M He; Isabelle J Pouliquen; Malcolm I Mitchell
Journal:  Br J Clin Pharmacol       Date:  2002-09       Impact factor: 4.335

Review 2.  Safety and tolerability of moxonidine in the treatment of hypertension.

Authors:  M Schachter; J Luszick; B Jäger; C Verboom; E Söhlke
Journal:  Drug Saf       Date:  1998-09       Impact factor: 5.606

  2 in total

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