Effects of ketoprofen and ibuprofen on platelet aggregation and prostanoid formation in man.

Abstract:

OBJECTIVE:In the present randomized, fourway crossover study we determined the effects of two oral doses each of ketoprofen and ibuprofen on platelet aggregation and prostanoid formation in man. METHODS:Twelve healthy female volunteers received for 2 consecutive days, followed by a 5-day drug-free interval, one of the following: ketoprofen 3 x 25 mg per day, or ketoprofen 3 x 50 mg per day, or ibuprofen 3 x 200 mg per day, or ibuprofen 3 x 400 mg per day. The response criteria, determined before and on the 2nd day of each treatment period, were: maximal platelet aggregation in response to 1.0 mmol.l-1 arachidonic acid measured by the method of Born and Cross, thromboxane B2 (TXB2) concentration in platelet-rich plasma after aggregation measured by radioimmunoassay, and PGE-M, the index metabolite of total body prostaglandin E2 (PGE2) production, assessed by gas chromatography/tandem mass spectrometry using 18O2-PGE-M as internal standard. RESULTS:Platelet aggregation was significantly reduced by ketoprofen 3 x 25 mg per day (-57%) and ketoprofen 3 x 50 mg per day (-85%) as compared to control, whereas ibuprofen 3 x 200 mg per day (-3%) and ibuprofen 3 x 400 mg per day (-22%) had no significant effects. TXB2 synthesis was significantly decreased by ketoprofen 3 x 25 mg per day (-72%), ketoprofen 3 x 50 mg per day (-97%) and ibuprofen 3 x 400 mg per day (-48%) as compared to control; ibuprofen 3 x 200 mg per day did not reduce TXB2 formation significantly (-23%). All four treatments reduced 24-h urinary excretion of PGE-M significantly in the range of -39% (ketoprofen 3 x 25 mg per day) to -53% (ibuprofen 3 x 400 mg per day) without significant differences between treatments. CONCLUSION:Our data show that both ketoprofen dosages were more effective in inhibition of platelet aggregation and platelet thromboxane synthesis than ibuprofen in low or high dosage. Total body synthesis of the E-prostaglandins was inhibited by all drug schedules without significant differences between treatments.

journal_name

Eur J Clin Pharmacol

authors

Stichtenoth DO,Tsikas D,Gutzki FM,Frölich JC

doi

10.1007/s002280050189

subject

Has Abstract

pub_date

1996-01-01 00:00:00

pages

231-4

issue

3-4

eissn

0031-6970

issn

1432-1041

journal_volume

51

pub_type

临床试验,杂志文章,随机对照试验
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    pub_type: 临床试验,杂志文章,随机对照试验

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    pub_type: 杂志文章

    doi:10.1007/BF02284968

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    doi:10.1007/s00228-010-0932-0

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  • Effect of ketoconazole on venlafaxine plasma concentrations in extensive and poor metabolisers of debrisoquine.

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    pub_type: 临床试验,杂志文章

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    journal_title:European journal of clinical pharmacology

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    doi:10.1007/BF00315310

    authors: Newnham DM,Coutie WJ,McFarlane LC,Lipworth BJ

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    journal_title:European journal of clinical pharmacology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/BF00562056

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  • Impact of regional copayment policy on selective serotonin reuptake inhibitor (SSRI) consumption and expenditure in Italy.

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  • Long acting beta-blockers in the twenty fourth hour.

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    journal_title:European journal of clinical pharmacology

    pub_type: 临床试验,杂志文章

    doi:10.1007/BF00542508

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    更新日期:1983-01-01 00:00:00

  • Vancomycin-induced nephrotoxicity: mechanism, incidence, risk factors and special populations. A literature review.

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    journal_title:European journal of clinical pharmacology

    pub_type: 杂志文章,评审

    doi:10.1007/s00228-012-1259-9

    authors: Elyasi S,Khalili H,Dashti-Khavidaki S,Mohammadpour A

    更新日期:2012-09-01 00:00:00

  • A systematic review and meta-analysis of microbial contamination of parenteral medication prepared in a clinical versus pharmacy environment.

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    pub_type: 杂志文章,meta分析,评审

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  • Quality and impact of problem-oriented drug information: a method to change clinical practice among physicians?

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    pub_type: 杂志文章

    doi:10.1007/s00228-001-0386-5

    authors: Schjøtt J,Pomp E,Gedde-Dahl A

    更新日期:2002-02-01 00:00:00

  • Genetic polymorphism of CYP2C19 and lansoprazole pharmacokinetics in Japanese subjects.

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    doi:10.1007/s002280050307

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    更新日期:1997-01-01 00:00:00

  • Integrating pharmacogenetics and therapeutic drug monitoring: optimal dosing of imatinib as a case-example.

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