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首页> 外文期刊>Neurourology and urodynamics. >Changes in nitric oxide production in the rat kidney due to CaOx nephrolithiasis.
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Changes in nitric oxide production in the rat kidney due to CaOx nephrolithiasis.

机译:CaOx肾结石症导致大鼠肾脏中一氧化氮产生的变化。

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摘要

AIMS: The aim of the study was to test the hypothesis that the renal nitric oxide (NO) system is involved in the animal model of nephrolithiasis by evaluating the relationship between nitric oxide synthase (NOS) and oxidative stress. METHODS: Deposition of renal calculi was induced by adding 0.75% ethylene glycol (EG) to the drinking water of male Wistar rats. After 42 days of treatment, urinary biochemistry and urinary levels of oxalate, NO metabolites (nitrate and nitrite), cGMP, and lipid peroxides, and markers for renal damage and oxidative stress in the kidney were examined. In the second part of the experiment, two diuretic stimuli (intrarenal infusion of l-arginine or saline loading) were applied to test the renal NO system response. Finally, levels of three isoforms of NOS in renal tissues were evaluated by immunostaining. RESULTS: In the EG-treated rats, increased urinary excretion of enzymes and lipid peroxides and increased nitrotyrosine levels and oxidative injury markers in the kidneys indicated that peroxynitrite formation occurred during oxidative stress, while the 24-hr urinary excretion of NO metabolites and cGMP remained unchanged. In contrast to control rats, urinary excretion and NO metabolites and cGMP excretion were unresponsive to intrarenal l-arginine infusion; in response to saline loading, an increase in these factors was seen, but the increase was only 50% of that seen in the identically treated control group. A significant decrease in eNOS expression and increase in iNOS expression were observed in the renal medulla of the EG-treated group, whereas expression of nNOS was not affected. CONCLUSIONS: Although basal renal NO production remained unchanged, excessive peroxynitrite formation in the kidney was noted in this model. A decreased response of the NOS system was noted when diuretic stimuli were applied. How the imbalance between eNOS and iNOS expression influences CaOx stone formation requires detailed evaluation.
机译:目的:该研究的目的是通过评估一氧化氮合酶(NOS)与氧化应激之间的关系,来检验肾一氧化氮(NO)系统参与肾结石症动物模型的假设。方法:在雄性Wistar大鼠的饮用水中加入0.75%的乙二醇(EG)诱导肾结石沉积。治疗42天后,检查了尿中的草酸,NO代谢产物(硝酸盐和亚硝酸盐),cGMP和脂质过氧化物的尿生化和尿水平,以及肾脏中肾脏损害和氧化应激的标志物。在实验的第二部分中,应用了两种利尿剂刺激(肾内输注L-精氨酸或生理盐水)来测试肾脏NO系统反应。最后,通过免疫染色评估了肾脏组织中三种NOS亚型的水平。结果:在接受EG治疗的大鼠中,肾脏中酶和脂质过氧化物的尿排泄增加,肾脏中的硝基酪氨酸水平和氧化损伤标志物增加,表明在氧化应激期间发生过氧亚硝酸盐形成,而24小时NO代谢产物和cGMP的尿排泄仍然存在不变。与对照组相比,尿内排泄,NO代谢产物和cGMP排泄对肾内L-精氨酸输注无反应。响应于盐负荷,这些因素有所增加,但增加幅度仅为相同治疗对照组的50%。在EG治疗组的肾延髓中观察到eNOS表达的显着降低和iNOS表达的增加,而nNOS的表达未受影响。结论:尽管基础肾脏NO的产生保持不变,但在该模型中注意到肾脏中过多的过氧亚硝酸盐形成。使用利尿剂时,注意到NOS系统的反应降低。 eNOS和iNOS表达之间的不平衡如何影响CaOx结石形成需要详细评估。

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