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膳食硝酸盐补充可改善慢性缺血中的再血管化。

Dietary nitrate supplementation improves revascularization in chronic ischemia.

机构信息

Division of Cardiology, Pulmonology and Vascular Medicine, Medical Faculty, University Hospital Düsseldorf, Düsseldorf, Germany.

出版信息

Circulation. 2012 Oct 16;126(16):1983-92. doi: 10.1161/CIRCULATIONAHA.112.112912. Epub 2012 Sep 19.

Abstract

BACKGROUND

Revascularization is an adaptive repair mechanism that restores blood flow to undersupplied ischemic tissue. Nitric oxide plays an important role in this process. Whether dietary nitrate, serially reduced to nitrite by commensal bacteria in the oral cavity and subsequently to nitric oxide and other nitrogen oxides, enhances ischemia-induced remodeling of the vascular network is not known.

METHODS AND RESULTS

Mice were treated with either nitrate (1 g/L sodium nitrate in drinking water) or sodium chloride (control) for 14 days. At day 7, unilateral hind-limb surgery with excision of the left femoral artery was conducted. Blood flow was determined by laser Doppler. Capillary density, myoblast apoptosis, mobilization of CD34(+)/Flk-1(+), migration of bone marrow-derived CD31(+)/CD45(-), plasma S-nitrosothiols, nitrite, and skeletal tissue cGMP levels were assessed. Enhanced green fluorescence protein transgenic mice were used for bone marrow transplantation. Dietary nitrate increased plasma S-nitrosothiols and nitrite, enhanced revascularization, increased mobilization of CD34(+)/Flk-1(+) and migration of bone marrow-derived CD31(+)/CD45(-) cells to the site of ischemia, and attenuated apoptosis of potentially regenerative myoblasts in chronically ischemic tissue. The regenerative effects of nitrate treatment were abolished by eradication of the nitrate-reducing bacteria in the oral cavity through the use of an antiseptic mouthwash.

CONCLUSIONS

Long-term dietary nitrate supplementation may represent a novel nutrition-based strategy to enhance ischemia-induced revascularization.

摘要

背景

再血管化是一种适应性修复机制,可恢复向缺血组织提供的血流。一氧化氮在这个过程中起着重要作用。尚不清楚饮食硝酸盐(通过口腔共生细菌连续还原为亚硝酸盐,随后还原为一氧化氮和其他氮氧化物)是否增强缺血诱导的血管网络重塑。

方法和结果

小鼠用硝酸盐(饮用水中 1 g/L 硝酸钠)或氯化钠(对照)处理 14 天。第 7 天,进行单侧后肢手术,切除左侧股动脉。通过激光多普勒测定血流。评估毛细血管密度、成肌细胞凋亡、CD34(+)/Flk-1(+)动员、骨髓源性 CD31(+)/CD45(-)迁移、血浆 S-亚硝基硫醇、亚硝酸盐和骨骼组织 cGMP 水平。使用增强型绿色荧光蛋白转基因小鼠进行骨髓移植。饮食硝酸盐增加了血浆 S-亚硝基硫醇和亚硝酸盐,增强了再血管化,增加了 CD34(+)/Flk-1(+)的动员和骨髓源性 CD31(+)/CD45(-)细胞向缺血部位的迁移,并减轻了慢性缺血组织中成肌细胞的潜在再生性凋亡。通过使用防腐剂漱口水消除口腔中的硝酸盐还原菌,硝酸盐处理的再生作用被消除。

结论

长期饮食硝酸盐补充可能代表一种增强缺血诱导再血管化的新型营养策略。

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