Matches in SemOpenAlex for { <https://semopenalex.org/work/W4214571844> ?p ?o ?g. }
- W4214571844 endingPage "3246" @default.
- W4214571844 startingPage "3234" @default.
- W4214571844 abstract "Background: Abnormal proliferation of vascular smooth muscle cells (VSMCs) in the intimal region is a key event in the development of neointimal hyperplasia. 10-G, a bioactive compound found in ginger, exerted inhibitory effects on the proliferation of several cancer cells. However, the effect and mechanism of 10-G on neointimal hyperplasia are not clear. Purpose: To explore the suppressive effects of 10-G on the proliferation and migration of VSMCs, and investigate the underlying mechanisms. Methods: In vivo, a left common carotid artery ligation mouse model was used to observe the effects of neointimal formation through immunohistochemistry and hematoxylin-eosin staining. In vitro, the cell proliferation and migration of HASMCs and A7r5 cells were detected by MTS assay, EdU staining, wound healing assay, Transwell assay, and western blotting as well. Molecular docking, molecular dynamics simulations and surface plasmon resonance imaging were collectively used to evaluate the interaction of 10-G with AMP-activated protein kinase (AMPK). Compound C and si-AMPK were used to inhibit the expression of AMPK. Results: Treatment with 10-G significantly reduced neointimal hyperplasia in the left common carotid artery ligation mouse model. MST and EdU staining showed that 10-G inhibited the proliferation of VSMC cells A7r5 and HASMC. We also found that 10-G altered the expression of proliferation-related proteins, including CyclinD1, CyclinD2, CyclinD3, and CDK4. Molecular docking revealed that the binding energy between AMPK and 10-G is -7.4 kcal mol-1. Molecular simulations suggested that the binding between 10-G and AMPK is stable. Surface plasmon resonance imaging analysis also showed that 10-G has a strong binding affinity to AMPK (KD = 6.81 × 10-8 M). 10-G promoted AMPKα phosphorylation both in vivo and in vitro. Blocking AMPK by an siRNA or AMPK inhibitor pathway partly abolished the anti-proliferation effects of 10-G on VSMCs. Conclusion: These data showed that 10-G might inhibit neointimal hyperplasia and suppress VSMC proliferation by the activation of AMPK as a natural AMPK agonist." @default.
- W4214571844 created "2022-03-02" @default.
- W4214571844 creator A5002583040 @default.
- W4214571844 creator A5021669690 @default.
- W4214571844 creator A5021782944 @default.
- W4214571844 creator A5022896962 @default.
- W4214571844 creator A5030458072 @default.
- W4214571844 creator A5038427797 @default.
- W4214571844 creator A5045706719 @default.
- W4214571844 creator A5052651640 @default.
- W4214571844 creator A5054831917 @default.
- W4214571844 creator A5056342535 @default.
- W4214571844 creator A5073574375 @default.
- W4214571844 creator A5081451260 @default.
- W4214571844 creator A5084130934 @default.
- W4214571844 date "2022-01-01" @default.
- W4214571844 modified "2023-10-14" @default.
- W4214571844 title "10-Gingerol, a natural AMPK agonist, suppresses neointimal hyperplasia and inhibits vascular smooth muscle cell proliferation" @default.
- W4214571844 cites W1024036315 @default.
- W4214571844 cites W1511269911 @default.
- W4214571844 cites W1963885748 @default.
- W4214571844 cites W1986899166 @default.
- W4214571844 cites W2027982316 @default.
- W4214571844 cites W2039768522 @default.
- W4214571844 cites W2056564326 @default.
- W4214571844 cites W2085567056 @default.
- W4214571844 cites W2098619012 @default.
- W4214571844 cites W2106903440 @default.
- W4214571844 cites W2111198326 @default.
- W4214571844 cites W2133301348 @default.
- W4214571844 cites W2171010297 @default.
- W4214571844 cites W2274680336 @default.
- W4214571844 cites W2313705475 @default.
- W4214571844 cites W2326531080 @default.
- W4214571844 cites W2568596714 @default.
- W4214571844 cites W2589445559 @default.
- W4214571844 cites W2590573757 @default.
- W4214571844 cites W2596314029 @default.
- W4214571844 cites W2696298149 @default.
- W4214571844 cites W2735956192 @default.
- W4214571844 cites W2740454899 @default.
- W4214571844 cites W2742734698 @default.
- W4214571844 cites W2746702337 @default.
- W4214571844 cites W2765285487 @default.
- W4214571844 cites W2883196957 @default.
- W4214571844 cites W2887726015 @default.
- W4214571844 cites W2897400078 @default.
- W4214571844 cites W2898927694 @default.
- W4214571844 cites W2944543781 @default.
- W4214571844 cites W2964445842 @default.
- W4214571844 cites W2968731587 @default.
- W4214571844 cites W2981807817 @default.
- W4214571844 cites W3002721650 @default.
- W4214571844 cites W3022520860 @default.
- W4214571844 cites W3043760418 @default.
- W4214571844 cites W3046719355 @default.
- W4214571844 cites W3047161397 @default.
- W4214571844 cites W3062144999 @default.
- W4214571844 cites W3084922787 @default.
- W4214571844 cites W3122226502 @default.
- W4214571844 cites W3188944453 @default.
- W4214571844 cites W3202971910 @default.
- W4214571844 cites W3216582714 @default.
- W4214571844 doi "https://doi.org/10.1039/d1fo03610f" @default.
- W4214571844 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35213678" @default.
- W4214571844 hasPublicationYear "2022" @default.
- W4214571844 type Work @default.
- W4214571844 citedByCount "1" @default.
- W4214571844 countsByYear W42145718442022 @default.
- W4214571844 crossrefType "journal-article" @default.
- W4214571844 hasAuthorship W4214571844A5002583040 @default.
- W4214571844 hasAuthorship W4214571844A5021669690 @default.
- W4214571844 hasAuthorship W4214571844A5021782944 @default.
- W4214571844 hasAuthorship W4214571844A5022896962 @default.
- W4214571844 hasAuthorship W4214571844A5030458072 @default.
- W4214571844 hasAuthorship W4214571844A5038427797 @default.
- W4214571844 hasAuthorship W4214571844A5045706719 @default.
- W4214571844 hasAuthorship W4214571844A5052651640 @default.
- W4214571844 hasAuthorship W4214571844A5054831917 @default.
- W4214571844 hasAuthorship W4214571844A5056342535 @default.
- W4214571844 hasAuthorship W4214571844A5073574375 @default.
- W4214571844 hasAuthorship W4214571844A5081451260 @default.
- W4214571844 hasAuthorship W4214571844A5084130934 @default.
- W4214571844 hasConcept C11960822 @default.
- W4214571844 hasConcept C126322002 @default.
- W4214571844 hasConcept C134018914 @default.
- W4214571844 hasConcept C1491633281 @default.
- W4214571844 hasConcept C185592680 @default.
- W4214571844 hasConcept C2778095995 @default.
- W4214571844 hasConcept C2778283817 @default.
- W4214571844 hasConcept C2778583881 @default.
- W4214571844 hasConcept C2779395532 @default.
- W4214571844 hasConcept C2780124434 @default.
- W4214571844 hasConcept C2992686903 @default.
- W4214571844 hasConcept C55493867 @default.
- W4214571844 hasConcept C62112901 @default.
- W4214571844 hasConcept C71924100 @default.
- W4214571844 hasConcept C86803240 @default.