Liu Qian, Zhang Ling, Shan Qiyuan, Ding Yuxia, Zhang Zhaocai, Zhu Meifei, Mao Yuanjie
1 College of Pharmaceutical Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
2 Department of Cardiology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
J Int Med Res. 2018 Jun;46(6):2096-2103. doi: 10.1177/0300060517717358. Epub 2017 Aug 31.
Objective To investigate the vasodilative and endothelial-protective effects and the underlying mechanisms of total flavonoids from Astragalus (TFA). Methods The vasodilative activities of TFA were measured with a myograph ex vivo using rat superior mesenteric arterial rings. The primary human umbilical vein endothelial cell (HUVEC) viabilities were assayed using the cell counting kit-8 after hypoxia or normoxia treatment with or without TFA. Akt, P-Akt, eNOS, P-eNOS, Erk, P-Erk, Bcl-2 and Bax expression were analyzed using western blotting. Results TFA showed concentration-dependent vasodilative effects on rat superior mesenteric arterial rings, but had no effects on normal or potassium chloride precontracted arterial rings. TFA did not affect HUVEC viabilities in normoxia, but dramatically promoted cell proliferation in the concentration range of 1 to 30 µg/mL under hypoxia. Moreover, TFA significantly increased the ratios of P-Akt/Akt and P-eNOS/eNOS in vascular endothelial cells under hypoxic conditions, but did not change the P-Erk/Erk or Bcl-2/Bax ratios. Conclusions TFA might exhibit vasorelaxant and endothelial-protective effects via the Akt/eNOS signaling pathway.
目的 探讨黄芪总黄酮(TFA)的血管舒张和内皮保护作用及其潜在机制。方法 使用大鼠肠系膜上动脉环,通过离体血管张力测定仪检测TFA的血管舒张活性。在用或不用TFA进行缺氧或常氧处理后,使用细胞计数试剂盒-8检测原代人脐静脉内皮细胞(HUVEC)的活力。采用蛋白质印迹法分析Akt、P-Akt、eNOS、P-eNOS、Erk、P-Erk、Bcl-2和Bax的表达。结果 TFA对大鼠肠系膜上动脉环具有浓度依赖性血管舒张作用,但对正常或氯化钾预收缩的动脉环无作用。TFA在常氧条件下不影响HUVEC活力,但在缺氧条件下,在1至30μg/mL浓度范围内显著促进细胞增殖。此外,TFA在缺氧条件下显著增加血管内皮细胞中P-Akt/Akt和P-eNOS/eNOS的比值,但不改变P-Erk/Erk或Bcl-2/Bax的比值。结论 TFA可能通过Akt/eNOS信号通路发挥血管舒张和内皮保护作用。