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Darapladib, a Lipoprotein-Associated Phospholipase A2 Inhibitor, Reduces Rho Kinase Activity in Atherosclerosis
Yonsei med. j ; Yonsei med. j;: 321-327, 2016.
Article de En | WPRIM | ID: wpr-147359
Bibliothèque responsable: WPRO
ABSTRACT
PURPOSE: Increased lipoprotein-associated phospholipase A2 (Lp-PLA2) activity and Rho kinase activity may be associated with atherosclerosis. The principal aim of this study was to examine whether darapladib (a selective Lp-PLA2 inhibitor) could reduce the elevated Lp-PLA2 and Rho kinase activity in atherosclerosis. MATERIALS AND METHODS: Studies were performed in male Sprague-Dawley rats. The atherosclerosis rats were prepared by feeding them with a high-cholesterol diet for 10 weeks. Low-dose darapladib (25 mg.kg-1.d-1) and high-dose darapladib (50 mg.kg-1.d-1) interventions were then administered over the course of 2 weeks. RESULTS: The serum levels of triglycerides, total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), high-sensitivity C-reactive protein (hs-CRP), and Lp-PLA2, significantly increased in atherosclerosis model groups, as did Rho kinase activity and cardiomyocyte apoptosis (p0.05). CONCLUSION: Darapladib, a Lp-PLA2 inhibitor, leads to cardiovascular protection that might be mediated by its inhibition of both Rho kinase and Lp-PLA2 in atherosclerosis.
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Texte intégral: 1 Indice: WPRIM Sujet Principal: Oximes / Triglycéride / Benzaldéhydes / Protéine C-réactive / Cholestérol / Rat Sprague-Dawley / 1-Alkyl-2-acetylglycerophosphocholine esterase / Relation dose-effet des médicaments / Athérosclérose / Rho-Associated Kinases Type d'étude: Prognostic_studies Limites du sujet: Animals langue: En Texte intégral: Yonsei med. j Année: 2016 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Oximes / Triglycéride / Benzaldéhydes / Protéine C-réactive / Cholestérol / Rat Sprague-Dawley / 1-Alkyl-2-acetylglycerophosphocholine esterase / Relation dose-effet des médicaments / Athérosclérose / Rho-Associated Kinases Type d'étude: Prognostic_studies Limites du sujet: Animals langue: En Texte intégral: Yonsei med. j Année: 2016 Type: Article