Quercetin downregulates NADPH oxidase, increases eNOS activity and prevents endothelial dysfunction in spontaneously hypertensive rats

被引:253
作者
Sánchez, M
Galisteo, M
Vera, R
Villar, IC
Zarzuelo, A
Tamargo, J
Pérez-Vizcaíno, F
Duarte, J [1 ]
机构
[1] Univ Granada, Sch Pharm, Dept Pharmacol, E-18071 Granada, Spain
[2] Univ Complutense Madrid, Sch Med, Dept Pharmacol, Madrid, Spain
关键词
caveolin; endothelial nitric oxide synthase; hypertension; NADPH oxidase; quercetin; spontaneously hypertensive rat; flavonoid;
D O I
10.1097/01.hjh.0000198029.22472.d9
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background and objective Several studies have found that chronic treatment with the dietary flavonoid quercetin lowers blood pressure and restores endothelial dysfunction in hypertensive animal models. We hypothesized that increased endothelial nitric oxide synthase (eNOS) and/or decreased nicotinamide adenine dinucleotide phosphate (NADPH) oxidase protein expression and activity, and reduced reactive oxygen species might be involved in the improvement of endothelial function induced by quercetin in sponataneously hypertensive rats (SHR). Design and methods Male SHR and Wistar-Kyoto (WKY) rats (5 weeks old) were treated with quercetin (10 mg/kg) or vehicle for 13 weeks. Changes in vascular expression of eNOS, caveolin-1 and p47(phox) were analysed by Western blot, eNOS activity by conversion of [H-3]arginine to L-[H-3]citrulline, and NADPH oxidase activity by NADPH-enhanced chemoluminescence of lucigenin. Results In SHR, quercetin reduced the increase in blood pressure and heart rate and enhanced the endothelium-dependent aortic vasodilation induced by acetylcholine, but had no effect on the endothelium-independent response induced by nitroprusside. However, quercetin had no effect on endothelium-dependent vasoconstriction and aortic thromboxane 132 production. Compared to WKY, SHR showed upregulated eNOS and p47(phox) protein expression, downregulated caveolin-1 expression, increased NADPH-induced superoxide production but, paradoxically, eNOS activity was reduced. Chronic quercetin treatment prevented all these changes in SHR. In WKY, quercetin had no effect on blood pressure, endothelial function or the expression or activity of the proteins analysed. Conclusions Enhanced eNOS activity and decreased NADPH oxidase-mediated superoxide anion (O-2(-)) generation associated with reduced p47(phox) expression appear to be essential mechanisms for the improvement of endothelial function and the anti hypertensive effects of chronic quercetin.
引用
收藏
页码:75 / 84
页数:10
相关论文
共 42 条
[31]   Different antioxidant effects of polyphenols on lipid peroxidation and hydroxyl radicals in the NADPH-, Fe-ascorbate- and Fe-microsomal systems [J].
Ozgová, D ;
Hermánek, J ;
Gut, I .
BIOCHEMICAL PHARMACOLOGY, 2003, 66 (07) :1127-1137
[32]   EFFECT OF INCREASED AVAILABILITY OF ENDOTHELIUM-DERIVED NITRIC-OXIDE PRECURSOR ON ENDOTHELIUM-DEPENDENT VASCULAR RELAXATION IN NORMAL SUBJECTS AND IN PATIENTS WITH ESSENTIAL-HYPERTENSION [J].
PANZA, JA ;
CASINO, PR ;
BADAR, DM ;
QUYYUMI, AA .
CIRCULATION, 1993, 87 (05) :1475-1481
[33]   Differential regulation of nitric oxide synthases and their allosteric regulators in heart and vessels of hypertensive rats [J].
Piech, A ;
Dessy, C ;
Havaux, X ;
Feron, O ;
Balligand, JL .
CARDIOVASCULAR RESEARCH, 2003, 57 (02) :456-467
[34]   Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NADH/NADPH oxidase activation - Contribution to alterations of vasomotor tone [J].
Rajagopalan, S ;
Kurz, S ;
Munzel, T ;
Tarpey, M ;
Freeman, BA ;
Griendling, KK ;
Harrison, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (08) :1916-1923
[35]  
RICEEVANS A, 1998, FLAVONOIDS HLTH DIS
[36]   Effect of hydrosoluble coenzyme Q10 on blood pressures and Insulin resistance in hypertensive patients with coronary artery disease [J].
Singh, RB ;
Niaz, MA ;
Rastogi, SS ;
Shukla, PK ;
Thakur, AS .
JOURNAL OF HUMAN HYPERTENSION, 1999, 13 (03) :203-208
[37]   Increased generation of superoxide by angiotensin II in smooth muscle cells from resistance arteries of hypertensive patients: role of phospholipase D-dependent NAD(P)H oxidase-sensitive pathways [J].
Touyz, RM ;
Schiffrin, EL .
JOURNAL OF HYPERTENSION, 2001, 19 (07) :1245-1254
[38]   Vitamins reverse endothelial dysfunction through regulation of eNOS and NAD(P)H oxidase activities [J].
Ülker, S ;
McKeown, PP ;
Bayraktutan, U .
HYPERTENSION, 2003, 41 (03) :534-539
[39]   Upregulation of renal and vascular nitric oxide synthase in young spontaneously hypertensive rats [J].
Vaziri, ND ;
Ni, ZM ;
Oveisi, F .
HYPERTENSION, 1998, 31 (06) :1248-1254
[40]   cGMP-mediated negative-feedback regulation of endothelial nitric oxide synthase expression by nitric oxide [J].
Vaziri, ND ;
Wang, XQ .
HYPERTENSION, 1999, 34 (06) :1237-1241