Literature DB >> 2612537

Monoamine uptake inhibition by plasma from healthy volunteers after single oral doses of the antidepressant milnacipran.

C Palmier1, C Puozzo, T Lenehan, M Briley.   

Abstract

In a placebo-controlled double-blind cross-over study, we gave 12 healthy male volunteers placebo or milnacipran orally, such that each volunteer received placebo and two doses of milnacipran. Blood samples taken before and at various times after dosing were analysed for plasma concentrations of unchanged milnacipran and the inhibitory effect of the plasma on the uptake of 3H-5-hydroxytryptamine (5HT) into normal human platelets or of 3H-noradrenaline into rat hypothalamus homogenate. The mean maximal inhibition of 5HT and noradrenaline uptake was correlated with drug dose. The inhibition of 5HT uptake was correlated with the inhibition of noradrenaline uptake and both were correlated with plasma concentration of unchanged drug at all times and doses tested. Thus, milnacipran, when given orally to man, circulates in a biologically active form with similar potency for the inhibition of 5HT and noradrenaline uptake.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2612537     DOI: 10.1007/bf00679776

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


  4 in total

1.  Biochemical profile of midalcipran (F 2207), 1-phenyl-1-diethyl-aminocarbonyl-2-aminomethyl-cyclopropane (Z) hydrochloride, a potential fourth generation antidepressant drug.

Authors:  C Moret; M Charveron; J P Finberg; J P Couzinier; M Briley
Journal:  Neuropharmacology       Date:  1985-12       Impact factor: 5.250

2.  Psychopharmacology of midalcipran, 1-phenyl-1-diethyl-amino-carbonyl-2-aminomethylcyclopropane hydrochloride (F 2207), a new potential antidepressant.

Authors:  A Stenger; J P Couzinier; M Briley
Journal:  Psychopharmacology (Berl)       Date:  1987       Impact factor: 4.530

3.  Inhibition of platelet uptake of serotonin in plasma from patients treated with clomipramine and amitriptyline.

Authors:  O Lingjaerde
Journal:  Eur J Clin Pharmacol       Date:  1979-06-12       Impact factor: 2.953

4.  1-Aryl-2-(aminomethyl)cyclopropanecarboxylic acid derivatives. A new series of potential antidepressants.

Authors:  B Bonnaud; H Cousse; G Mouzin; M Briley; A Stenger; F Fauran; J P Couzinier
Journal:  J Med Chem       Date:  1987-02       Impact factor: 7.446

  4 in total
  4 in total

1.  Effects of repeated milnacipran administration on brain serotonergic and noradrenergic functions in healthy volunteers.

Authors:  Atsushi Soya; Takeshi Terao; Mami Nakajima; Hideki Kojima; Tatsuya Okamoto; Yoshiaki Inoue; Miki Iwakawa; Koji Shinkai; Reiji Yoshimura; Yoichi Ueta; Jun Nakamura
Journal:  Psychopharmacology (Berl)       Date:  2006-07-08       Impact factor: 4.530

2.  Lack of interaction of milnacipran with the cytochrome p450 isoenzymes frequently involved in the metabolism of antidepressants.

Authors:  Christian Puozzo; Simone Lens; Christian Reh; Karl Michaelis; Dominique Rosillon; Xavier Deroubaix; Dominique Deprez
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

Review 3.  Milnacipran. A review of its use in depression.

Authors:  C M Spencer; M I Wilde
Journal:  Drugs       Date:  1998-09       Impact factor: 9.546

4.  Single- and Multiple-Dose Milnacipran Pharmacokinetics in Healthy Han Chinese Volunteers.

Authors:  Can-Jun Ruan; An-Ning Li; Fang Dong; Yi-Min Zhai; Wen-Biao Li; Chuan-Yue Wang; Jose de Leon
Journal:  Clin Pharmacokinet       Date:  2016-07       Impact factor: 6.447

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.