Antihypertensive effects of Tartary buckwheat flavonoids by improvement of vascular insulin sensitivity in spontaneously hypertensive rats

被引:34
|
作者
Hou, Zuoxu [1 ]
Hu, Yuanyuan [2 ,3 ]
Yang, Xingbin [3 ]
Chen, Wensheng [4 ]
机构
[1] Fourth Mil Med Univ, Dept Aerosp Med, Xian 710032, Shaanxi, Peoples R China
[2] Chongqing Univ Educ, Chongqing Collaborat Innovat Ctr Funct Food, Chongqing 400067, Peoples R China
[3] Shaanxi Normal Univ, Coll Food Engn & Nutrit Sci, Minist Educ Med Resource & Nat Pharmaceut Chem, Key Lab, Xian 710062, Shaanxi, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Cardiovasc Surg, Xian 710032, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
RANDOMIZED CONTROLLED-TRIAL; NITRIC-OXIDE; ENDOTHELIAL DYSFUNCTION; BLOOD-PRESSURE; CARDIOVASCULAR-DISEASE; RECEPTOR SUBSTRATE-1; OXIDATIVE STRESS; DOWN-REGULATION; HIGH GLUCOSE; RESISTANCE;
D O I
10.1039/c7fo00975e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vascular insulin resistance and oxidative stress contribute to endothelial dysfunction and hypertension. The present study investigated whether chronic treatment with purified Tartary buckwheat flavonoids fraction (TBF) prevents the development of hypertension via improving vascular insulin sensitivity and reducing oxidative stress. Six-week-old male spontaneously hypertensive rats (SHRs) and their normotensive Wistar-Kyoto (WKY) control rats were subjected to different dosages of TBF for 8 weeks. Blood pressure, mesenteric arteriolar vasorelaxation, superoxide anion (O-2(-)) generation, NAD(P) H oxidase activity, and insulin-stimulated Akt/endothelial nitric oxide synthase (eNOS) activation and nitric oxide (NO) production were determined. The SHRs had higher systolic blood pressure, systemic insulin resistance, and impaired vasodilator actions of insulin and the insulin signaling pathway in mesenteric arterioles when compared with the WKY rats. TBF treatment at a dosage of 100 mg kg(-1) day(-1) significantly reduced systolic blood pressure and increased vasodilator response to insulin in the SHRs. Additionally, TBF treatment significantly reduced phosphorylation of insulin receptor substrate 1 (IRS-1) at serine 307 and increased insulin-stimulated Akt/eNOS activation in the SHRs. Furthermore, TBF treatment reduced the overproduction of basal O-2(-) in association with a reduction of NAD(P) H oxidase activity in mesenteric arterioles of the SHRs. Finally, quercetin was identified as the predominant active component of TBF in attenuating the development of hypertension with regard to reducing vascular oxidative stress, regulating the vascular insulin signaling pathway and restoring vasodilator response to insulin in the SHRs. In conclusion, TBF possesses protective effects against hypertension through attenuating vascular insulin resistance and oxidative stress.
引用
收藏
页码:4217 / 4228
页数:12
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