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Antiplatelet effect of AMP-activated protein kinase activator and its potentiation by the phosphodiesterase inhibitor dipyridamole

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dc.contributor.authorLiu, Yingqiu-
dc.contributor.authorOh, Seok-Jeong-
dc.contributor.authorChang, Kyung-Hwa-
dc.contributor.authorKim, Yoon-Gyoon-
dc.contributor.authorLee, Moo-Yeol-
dc.date.accessioned2024-08-08T01:31:31Z-
dc.date.available2024-08-08T01:31:31Z-
dc.date.issued2013-10-01-
dc.identifier.issn0006-2952-
dc.identifier.issn1873-2968-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/15377-
dc.description.abstractAMP-activated protein kinase (AMPK) activates endothelial nitric oxide synthase (eNOS) via phosphorylation at the activating site. The eNOS-nitric oxide (NO)/soluble guanylate cyclase (sGC)-cGMP/cGMP-dependent protein kinase (PKG) signaling axis is a major antiaggregatory mechanism residing in platelets. Based on the hypothesis that direct activation of AMPK might be a potential strategy to inhibit platelet aggregation, the antiplatelet effect of AMPK activators was investigated. Treatment of isolated platelets with the AMPK activator, 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR) resulted in AMPK activation and a decrease in aggregation, which was abolished by pretreatment with the AMPK inhibitors compound C (CC) and ara-A. Such an AMPK-dependent antiaggregatory effect was also observed with other AMPK activators such as A-769662 and PT1. AICAR induced eNOS activation was followed by NO synthesis, cGMP production, and subsequent phosphorylation of vasodilator-stimulated phosphoprotein (VASP), a PKG substrate. All these events were blocked by CC or ara-A pretreatment, and each event was inhibited by the eNOS inhibitor L-NAME, the sGC inhibitor ODQ and the PKG inhibitor Rp-8-pCPT-cGMPS. Simultaneous treatment of dipyridamole, a phosphodiesterase (PDE) inhibitor, with AICAR potentiated the antiaggregatory effect by enhancing the cGMP elevation. Administration of AICAR increased platelet cGMP and prolonged FeCl3-induced arterial occlusion time in rats, which further increased in combination with dipyridamole. In conclusion, AMPK activators inhibited platelet aggregation by stimulating the eNOS-NO/sGC-cGMP/PKG signaling pathway. The antiplatelet effect of AMPK activators could be potentiated in combination with a PDE inhibitor through the common mechanism of elevating cGMP. Thus, AMPK may serve as a potential target for antiplatelet therapy. (c) 2013 Elsevier Inc. All rights reserved.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleAntiplatelet effect of AMP-activated protein kinase activator and its potentiation by the phosphodiesterase inhibitor dipyridamole-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.bcp.2013.07.009-
dc.identifier.scopusid2-s2.0-84884699320-
dc.identifier.wosid000324976900008-
dc.identifier.bibliographicCitationBIOCHEMICAL PHARMACOLOGY, v.86, no.7, pp 914 - 925-
dc.citation.titleBIOCHEMICAL PHARMACOLOGY-
dc.citation.volume86-
dc.citation.number7-
dc.citation.startPage914-
dc.citation.endPage925-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHASE-
dc.subject.keywordPlusENDOTHELIAL NO SYNTHASE-
dc.subject.keywordPlusPLATELET-AGGREGATION-
dc.subject.keywordPlusCARDIOVASCULAR-DISEASE-
dc.subject.keywordPlusTHERAPEUTIC TARGET-
dc.subject.keywordPlusSKELETAL-MUSCLE-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusARTERIAL THROMBOSIS-
dc.subject.keywordPlusMETABOLIC SYNDROME-
dc.subject.keywordPlusDRUG TARGET-
dc.subject.keywordAuthorAMP-activated protein kinase (AMPK)-
dc.subject.keywordAuthorPlatelet aggregation-
dc.subject.keywordAuthorAntiplatelet therapy-
dc.subject.keywordAuthorThrombosis 5-Aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR)-
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