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Lack of critical involvement of endothelial nitric oxide synthase in vascular nitrate tolerance in mice

机译:缺乏小鼠血管内皮硝酸盐耐受性的内皮一氧化氮合酶的关键参与

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摘要

We examined the direct involvement of endothelial nitric oxide (eNOS) in nitrate tolerance using eNOS knockout (eNOS (−/−)) and wild-type (eNOS (+/+)) mice. Animals were treated with either nitroglycerin (NTG, 20 mg kg−1s.c. 3×daily for 3 days) or vehicle (5% dextrose, D5W), and nitrate tolerance was assessed ex vivo in isolated aorta by vascular relaxation studies and cyclic GMP accumulation. Western blot was performed to determine NOS expression after NTG treatment. In both the eNOS (−/−) and (+/+) mice, the EC50 from NTG concentration-response curve was increased by ∼3 fold, and vascular cyclic GMP accumulation was similarly decreased after NTG pretreatment. Vascular tolerance did not lead to changes in eNOS protein expression in eNOS (+/+) mice. These results indicate that vascular nitrate tolerance was similarly induced in eNOS (−/−) and (+/+) mice, suggesting that eNOS may not be critically involved in nitrate tolerance development in mice.
机译:我们使用eNOS基因敲除(eNOS(-/-))和野生型(eNOS(+ / +))小鼠研究了内皮一氧化氮(eNOS)直接参与硝酸盐耐受性的问题。用硝酸甘油(NTG,每天20 µmg kg -1 sc 3次,每天3次)或溶媒(5%葡萄糖,D5W)处理动物,并通过离体主动脉离体评估硝酸盐耐受性血管松弛研究和循环GMP积累。进行蛋白质印迹以确定NTG处理后的NOS表达。在eNOS(-/-)和(+ / +)小鼠中,NTG浓度-响应曲线的EC50增加了约3倍,而NTG预处理后,血管循环GMP的积累也减少了。血管耐受性并未导致eNOS(+ / +)小鼠的eNOS蛋白表达发生变化。这些结果表明,在eNOS(-/-)和(+ / +)小鼠中类似地诱导了血管对硝酸盐的耐受性,表明eNOS可能与小鼠硝酸盐耐受性的发展无关。

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