通过多种机制通过化合物丹申滴剂抑制血管化
Yanfang Yang1, Liying Yuan1, Hui Xiong2
1College of Life Sciences, State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials of Ministry of Education, Nankai University, Tianjin, 300071, China.
概括
化合物丹申滴剂 (CDDP) 通过抑制Wnt/β-catenin通路并激活Sirt1.1,有效地减少小鼠和细胞的血管化. 这种传统中医药在改善心血管疾病风险因素方面发挥了新的治疗作用.
科学领域:
- 心血管研究研究心血管研究
- 药理学 药理学是指药理学的学科.
- 细胞生物学 细胞生物学
背景情况:
- 血管化是一种被忽视的心血管疾病风险因素,缺乏特定的治疗方法.
- 化合物丹申滴液 (CDDP) 用于心血管疾病,但其对血管化的作用尚未研究.
研究的目的:
- 调查CDDP对ApoE-/-小鼠和体外血管化的影响.
- 阐明CDDP对血管化的作用的潜在机制.
主要方法:
- 网络药理学分析以预测CDDP的潜力.
- 在体内研究:ApoE-/-小鼠吃高脂肪饮食并补充CDDP.
- 在体外研究:暴露于CDDP的人类大动脉光滑肌细胞 (HASMC) 和内皮细胞 (HUVEC,HAEC).
主要成果:
- 在动脉样硬化病变和培养细胞中,CDDP减少了内脏化.
- 这些机制涉及通过DKK1/LRP6上调和减少骨质细胞标记物来抑制Wnt/β-catenin通路.
- 通过激活Sirt1和减少促炎性细胞因子,CDDP逆转了血管衰老和衰老.
结论:
- 通过调节DKK1/LRP6/β-catenin通路和EC-SMC交叉声调节,CDDP可以改善血管化.
- 通过Sirt1激活,CDDP减少了血管细胞衰老,突出了其治疗潜力.
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