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人体内纤连蛋白合成的同位素测定

Isotopic determination of fibronectin synthesis in humans.

作者信息

Carraro F, Rosenblatt J, Wolfe R R

机构信息

Metabolism Unit, Shriners Burns Institute, Galveston, TX 77550.

出版信息

Metabolism. 1991 Jun;40(6):553-61. doi: 10.1016/0026-0495(91)90043-v.

Abstract

Fibronectin is an opsonic protein that, among other functions, activates the reticuloendothelial system. Accurate measurement of its rate of synthesis is necessary to more fully understand its physiological role in normal and pathological conditions. We have determined the rate of fibronectin synthesis in three normal volunteers using a primed-constant infusion of 15N-glycine and 1,2-13C-leucine, and measuring the incorporation of the isotopes into the protein over 5 days of infusion. In nine additional subjects, the fractional synthetic rate (FSR) of fibronectin was calculated during a 24-hour infusion using urinary hippurate and plasma alpha-ketoisocaproic acid enrichment to represent the precursors for incorporation of labeled glycine and leucine, respectively, into fibronectin. The FSR using glycine and leucine was 1.56 +/- 0.14 and 1.29 +/- 0.04 (%/h), respectively, in the 5-day infusion study, and 1.56 +/- 0.10 versus 1.83 +/- 0.09 (%/h), respectively, in the 24-hour study. The results of the 5-day infusion of 15N-glycine justify the use of urinary hippurate to reflect the precursor enrichment for the determination of the FSR of fibronectin during a shorter (less than 24 hour) infusion period.

摘要

纤连蛋白是一种调理素蛋白,除其他功能外,还可激活网状内皮系统。准确测量其合成速率对于更全面地了解其在正常和病理状态下的生理作用是必要的。我们使用15N-甘氨酸和1,2-13C-亮氨酸的预充恒速输注法,并在输注的5天内测量同位素掺入该蛋白的情况,测定了三名正常志愿者体内纤连蛋白的合成速率。在另外九名受试者中,通过使用尿马尿酸盐和血浆α-酮异己酸富集分别代表标记的甘氨酸和亮氨酸掺入纤连蛋白的前体,在24小时输注期间计算纤连蛋白的分数合成率(FSR)。在为期5天的输注研究中,使用甘氨酸和亮氨酸的FSR分别为1.56±0.14和1.29±0.04(%/小时),在24小时研究中分别为1.56±0.10和1.83±0.09(%/小时)。15N-甘氨酸5天输注的结果证明,在较短(少于24小时)的输注期间,使用尿马尿酸盐反映前体富集以测定纤连蛋白的FSR是合理的。

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