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Article type: Research Article
Authors: Zhang, Jianboa; * | Shi, Qiyub | Hu, Yamina | Li, Xiaohongc
Affiliations: [a] Department Cardiology 6, Cangzhou Central Hospital, Cangzhou, Hebei, China | [b] Gastroenterology Department, Cangzhou People’s Hospital, Cangzhou, Hebei, China | [c] Department Cardiology 3, Cangzhou Central Hospital, Cangzhou, Hebei, China
Correspondence: [*] Corresponding author: Jianbo Zhang, Department Cardiology 6, Cangzhou Central Hospital, 16 Xinhuaxi Road, Cangzhou 061001, Hebei, China. Tel.: +86 18713686699; E-mail: 20204171@stu.hebmu.edu.cn.
Abstract: BACKGROUND:Diabetes mellitus (DM) abolishes the antithrombotic effect of Clopidogrel. Here, we investigated the synergistic effect of Silibinin on Clopidogrel-mediated atherosclerosis treatment in diabetic mice. METHODS:ApoE–/– mice were fed with high-fat diet (HFD) to establish the atherosclerotic model with diabetes. Animals were treated with Clopidogrel, Silibinin, or the combined to evaluate the protective effects on atherosclerosis and diabetes through Oil-red-O staining, qRT-PCR, Western blot, and metabolic measurements. Platelet activation and aggregation ex vivo assays were performed to detect the anti-thrombotic effect of different administrations. RESULTS:Silibinin significantly enhanced the inhibitory effect of Clopidogrel on atherosclerosis in DM mice. Co-administration of Silibinin with Clopidogrel remarkedly reduced the aortic lesion, inflammation, and endothelial dysfunction in aorta roots, and diabetic symptoms were significantly improved by the Silibinin-Clopidogrel treatment in HFD-fed ApoE–/– mice. Interestingly, the anti-thrombotic effect of Clopidogrel was further augmented by the Silibinin treatment in atherosclerotic mice. CONCLUSION:In atherosclerotic mouse model, Silibinin significantly improves the effect of Clopidogrel on atherosclerosis.
Keywords: Atherosclerosis, diabetes, Clopidogrel, Silibinin, platelet reactivity
DOI: 10.3233/CH-211279
Journal: Clinical Hemorheology and Microcirculation, vol. 80, no. 4, pp. 353-361, 2022
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