首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Whole body nitric oxide synthesis in healthy men determined from 15N arginine-to-15Ncitrulline labeling.
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Whole body nitric oxide synthesis in healthy men determined from 15N arginine-to-15Ncitrulline labeling.

机译:从15N精氨酸到15N瓜氨酸标签确定健康男性的全身一氧化氮合成。

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摘要

The rates of whole body nitric oxide (NO) synthesis, plasma arginine flux, and de novo arginine synthesis and their relationships to urea production, were examined in a total of seven healthy adults receiving an L-amino acid diet for 6 days. NO synthesis was estimated by the rate of conversion of the [15N] guanidino nitrogen of arginine to plasma [15N] ureido citrulline and compared with that based on urinary nitrite (NO2-)itrate (NO3-) excretion. Six subjects received on dietary day 7, a 24-hr (12-hr fed/12-hr fasted) primed, constant, intravenous infusion of L-[guanidino-15N2]arginine and [13C]urea. A similar investigation was repeated with three of these subjects, plus an additional subject, in which they received L-[ureido-13C]citrulline, to determine plasma citrulline fluxes. The estimated rates (mean +/- SD) of NO synthesis over a period of 24 hr averaged 0.96 +/- 0.1 mumol .kg-1.hr-1 and 0.95 +/- 0.1 mumol.kg-1.hr-1, for the [15N]citrulline and the nitriteitrate methods, respectively. About 15% of the plasma arginine turnover was associated with urea formation and 1.2% with NO formation. De novo arginine synthesis averaged 9.2 +/- 1.4 mumol. kg-1.hr-1, indicating that approximately 11% of the plasma arginine flux originates via conversion of plasma citrulline to arginine. Thus, the fraction of the plasma arginine flux associated with NO and also urea synthesis in healthy humans is small, although the plasma arginine compartment serves as a significant precursor pool (54%) for whole body NO formation. This tracer model should be useful for exploring these metabolic relationships in vivo, under specific pathophysiologic states where the L-arginine-NO pathway might be altered.
机译:在总共7名接受L-氨基酸饮食6天的健康成年人中,检查了全身一氧化氮(NO)合成速率,血浆精氨酸通量和从头精氨酸合成速率及其与尿素生成的关系。通过将精氨酸的[15N]胍基氮转化为血浆[15N]脲基瓜氨酸的速率估算NO的合成,并将其与基于亚硝酸尿(NO2-)/硝酸盐(NO3-)排泄的转化率进行比较。在饮食的第7天,接受了24小时(12小时进食/ 12小时禁食)的L- [胍基15N2]精氨酸和[13C]尿素灌注的恒定,静脉内输注的六名受试者。对其中三名受试者以及另外一名受试者(其中他们接受L- [ureido-13C]瓜氨酸)进行了类似的研究,以确定血浆瓜氨酸通量。 24小时内NO合成的估算速率(平均值+/- SD)平均为0.96 +/- 0.1μmol.kg-1.hr-1和0.95 +/- 0.1μmol.kg-1.hr-1,分别用于[15N]瓜氨酸和亚硝酸盐/硝酸盐方法。血浆精氨酸转化率的大约15%与尿素形成有关,而1.2%与NO形成有关。从头精氨酸合成平均为9.2 +/-1.4μmol。 kg-1.hr-1,表明血浆精氨酸通量的大约11%来自血浆瓜氨酸转化为精氨酸。因此,尽管精氨酸血浆区室是全身NO形成的重要前体库(54%),但与血浆NO有关的血浆精氨酸通量与健康人尿素合成的比例很小。该示踪剂模型对于在可能改变L-精氨酸-NO途径的特定病理生理状态下体内探索这些代谢关系方面应该是有用的。

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