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A dual PPAR alpha/gamma agonist increases adiponectin and improves plasma lipid profiles in healthy subjects.
Decochez, Katelijn; Rippley, Ronda K; Miller, Jutta L; De Smet, Marina; Yan, Kerri X; Matthijs, Zissi; Riffel, Kerry A; Song, Hengchang; Zhu, Haiyuan; Maynor, Hannah O; Tanaka, Wesley; Johnson-Levonas, Amy O; Davies, Michael J; Gottesdiener, Keith M; Keymeulen, Bart; Wagner, John A.
Afiliação
  • Decochez K; Diabetes Unit, Department of Endocrinology, Academic Hospital, Brussels Free University - VUB, Brussels, Belgium.
Drugs R D ; 7(2): 99-110, 2006.
Article em En | MEDLINE | ID: mdl-16542056
BACKGROUND: The objective of these studies was to evaluate the pharmacokinetics and pharmacodynamics of MK-0767, a prototypical dual peroxisome proliferator-activated receptor (PPAR) alpha/gamma agonist, following administration of single and multiple oral doses in healthy male subjects. METHODS: The first study was a double-blind, randomised, placebo-controlled, alternating two-panel, rising dose protocol in which single doses of 1-80 mg of MK-0767 were administered. The second study was a double-blind, randomised, placebo-controlled, staggered incremental dose, parallel-group protocol in which multiple doses of 0.3-25 mg of MK-0767 were administered once daily for 14 days. In both studies at each dose level, six subjects received MK-0767 and two subjects received placebo. RESULTS: Plasma area under the concentration-time curve and maximum plasma concentration increased with single and multiple doses of MK-0767 over the dose ranges studied. The apparent terminal half-life of MK-0767 averaged approximately 36 hours following single and multiple doses. Steady-state plasma concentrations were achieved following approximately 8 days of multiple doses. Compared with placebo, MK-0767 produced dose-dependent reductions in triglycerides (-26 +/- 8% [p = 0.002] and -33 +/- 13% [p = 0.008]) and free fatty acids (-50 +/- 11% [p < 0.001] and -67 +/- 23% [p = 0.008]) following single and multiple doses, respectively. Significant (p < or = 0.050) dose-dependent alterations in adiponectin (332 +/- 36%), low-density lipoprotein cholesterol (-29 +/- 5%), total cholesterol (-19 +/- 3%), non-high-density lipoprotein cholesterol (-28 +/- 4%), and fasting plasma glucose (-6 +/- 2%; only in the 25 mg group) were observed after multiple doses. CONCLUSIONS: The observed effects of MK-0767 on adiponectin, free fatty acids and lipids, even after single doses, demonstrate that this prototypical dual PPAR alpha/gamma agonist has clinically meaningful activity in vivo.
Assuntos
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Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Tiazóis / PPAR alfa / PPAR gama / Adiponectina / Lipídeos Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: Drugs R D Ano de publicação: 2006 Tipo de documento: Article
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Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Tiazóis / PPAR alfa / PPAR gama / Adiponectina / Lipídeos Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: Drugs R D Ano de publicação: 2006 Tipo de documento: Article