Nitrate decreases xanthine oxidoreductase-mediated nitrite reductase activity and attenuates vascular and blood pressure responses to nitrite

被引:25
|
作者
Damacena-Angelis, Celio [1 ]
Oliveira-Paula, Gustavo H. [2 ]
Pinheiro, Lucas C. [2 ]
Crevelin, Eduardo J. [3 ]
Portella, Rafael L. [2 ]
Moraes, Luiz Alberto B. [3 ]
Tanus-Santos, Jose E. [2 ]
机构
[1] Univ Estadual Campinas, Dept Pharmacol, Fac Med Sci, Campinas, SP, Brazil
[2] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Pharmacol, Av Bandeirantes 3900, BR-14049900 Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Sch Philosophy Sci & Languages, Dept Chem, Ribeirao Preto, SP, Brazil
来源
REDOX BIOLOGY | 2017年 / 12卷
基金
巴西圣保罗研究基金会;
关键词
Hypertension; Nitric oxide; Nitrite; Nitrate; Xanthine oxidoreductase; ORAL SODIUM-NITRITE; REACTIVE SPECIES GENERATION; OXIDE; MECHANISMS; BIOLOGY; EXPRESSION; INCREASE;
D O I
10.1016/j.redox.2017.03.003
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
Nitrite and nitrate restore deficient endogenous nitric oxide (NO) production as they are converted back to NO, and therefore complement the classic enzymatic NO synthesis. Circulating nitrate and nitrite must cross membrane barriers to produce their effects and increased nitrate concentrations may attenuate the nitrite influx into cells, decreasing NO generation from nitrite. Moreover, xanthine oxidoreductase (XOR) mediates NO formation from nitrite and nitrate. However, no study has examined whether nitrate attenuates XOR-mediated NO generation from nitrite. We hypothesized that nitrate attenuates the vascular and blood pressure responses to nitrite either by interfering with nitrite influx into vascular tissue, or by competing with nitrite for XOR, thus inhibiting XOR-mediated NO generation. We used two independent vascular function assays in rats (aortic ring preparations and isolated mesenteric arterial bed perfusion) to examine the effects of sodium nitrate on the concentration-dependent responses to sodium nitrite. Both assays showed that nitrate attenuated the vascular responses to nitrite. Conversely, the aortic responses to the NO donor DETANONOate were not affected by sodium nitrate. Further confirming these results, we found that nitrate attenuated the acute blood pressure lowering effects of increasing doses of nitrite infused intravenously in freely moving rats. The possibility that nitrate could compete with nitrite and decrease nitrite influx into cells was tested by measuring the accumulation of nitrogen-15-labeled nitrite (15N-nitrite) by aortic rings using ultra-performance liquid chromatography tandem mass-spectrometry (UPLC-MS/MS). Nitrate exerted no effect on aortic accumulation of 15N-nitrite. Next, we used chemiluminescence-based NO detection to examine whether nitrate attenuates XOR-mediated nitrite reductase activity. Nitrate significantly shifted the Michaelis Menten saturation curve to the right, with a 3-fold increase in the Michaelis constant. Together, our results show that nitrate inhibits XOR-mediated NO production from nitrite, and this mechanism may explain how nitrate attenuates the vascular and blood pressure responses to nitrite.
引用
收藏
页码:291 / 299
页数:9
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