Cited 28 time in
Antiplatelet effect of AMP-activated protein kinase activator and its potentiation by the phosphodiesterase inhibitor dipyridamole
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Liu, Yingqiu | - |
| dc.contributor.author | Oh, Seok-Jeong | - |
| dc.contributor.author | Chang, Kyung-Hwa | - |
| dc.contributor.author | Kim, Yoon-Gyoon | - |
| dc.contributor.author | Lee, Moo-Yeol | - |
| dc.date.accessioned | 2024-08-08T01:31:31Z | - |
| dc.date.available | 2024-08-08T01:31:31Z | - |
| dc.date.issued | 2013-10-01 | - |
| dc.identifier.issn | 0006-2952 | - |
| dc.identifier.issn | 1873-2968 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/15377 | - |
| dc.description.abstract | AMP-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.extent | 12 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
| dc.title | Antiplatelet effect of AMP-activated protein kinase activator and its potentiation by the phosphodiesterase inhibitor dipyridamole | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1016/j.bcp.2013.07.009 | - |
| dc.identifier.scopusid | 2-s2.0-84884699320 | - |
| dc.identifier.wosid | 000324976900008 | - |
| dc.identifier.bibliographicCitation | BIOCHEMICAL PHARMACOLOGY, v.86, no.7, pp 914 - 925 | - |
| dc.citation.title | BIOCHEMICAL PHARMACOLOGY | - |
| dc.citation.volume | 86 | - |
| dc.citation.number | 7 | - |
| dc.citation.startPage | 914 | - |
| dc.citation.endPage | 925 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
| dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
| dc.subject.keywordPlus | NITRIC-OXIDE SYNTHASE | - |
| dc.subject.keywordPlus | ENDOTHELIAL NO SYNTHASE | - |
| dc.subject.keywordPlus | PLATELET-AGGREGATION | - |
| dc.subject.keywordPlus | CARDIOVASCULAR-DISEASE | - |
| dc.subject.keywordPlus | THERAPEUTIC TARGET | - |
| dc.subject.keywordPlus | SKELETAL-MUSCLE | - |
| dc.subject.keywordPlus | IN-VIVO | - |
| dc.subject.keywordPlus | ARTERIAL THROMBOSIS | - |
| dc.subject.keywordPlus | METABOLIC SYNDROME | - |
| dc.subject.keywordPlus | DRUG TARGET | - |
| dc.subject.keywordAuthor | AMP-activated protein kinase (AMPK) | - |
| dc.subject.keywordAuthor | Platelet aggregation | - |
| dc.subject.keywordAuthor | Antiplatelet therapy | - |
| dc.subject.keywordAuthor | Thrombosis 5-Aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR) | - |
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