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血浆和尿液中精氨酸加压素的放射免疫测定。

Radioimmunoassay of arginine vasopressin in the plasma and urine.

作者信息

Srámková J, Horký K, Dvoráková J

出版信息

Physiol Bohemoslov. 1979;28(5):399-409.

PMID:160049
Abstract

We introduced the radioimmunoassay (RIA) of arginine vasopressin (AVP) with standard AVP and antiserum to AVP (both Calibiochem). The sensitivity of the system was increased from the declared 4pg to 1 pg per tube by preparing AVP-125I of high specific activity (about 1,500 mCi/mg) and by modifying the reaction conditions. The sensitivity of the method was adequate for measuring AVP in urine and in concentrated plasma extracts, even under physiological conditions. Reliability of the results depended upon maintenance of approximately the same osmolarity in all the RIA samples. The mean plasma AVP level, uncorrected for AVP extraction losses, was 1.52 +/- 0.20 pg/ml for an ad libitum fluid intake; in fluid deprivation it rose in proportion to the osmolarity of the plasma to 5.83 +/- 0.42 pg/ml at 12 hours and to 19.09 +/- 4.51 pg/ml at 36 hours. Extraction recovery of added AVP was about 63%. The urinary AVP concentration varied according to the patients' state of hydratation from undetectable values at UOsm less than 200 mOsm/1 to a mean 16.5 +/- 7.9 pg/ml in the presence of an ad libitum fluid intake and to 29.1 +/- 7.5 pg/ml after 12 hours' and 117.2 +/- 13.7 pg/ml after 36 hours' deprivation of fluids.

摘要

我们采用标准抗利尿激素(AVP)和抗AVP血清(均购自Calibiochem),引入了抗利尿激素的放射免疫分析(RIA)方法。通过制备高比活度(约1,500mCi/mg)的AVP-125I并改变反应条件,该系统的灵敏度从每管宣称的4pg提高到了1pg。即使在生理条件下,该方法的灵敏度也足以测定尿液和浓缩血浆提取物中的AVP。结果的可靠性取决于所有RIA样品中渗透压大致保持相同。在随意饮水时,未经AVP提取损失校正的平均血浆AVP水平为1.52±0.20pg/ml;在禁水时,其随血浆渗透压升高而升高,12小时时升至5.83±0.42pg/ml,36小时时升至19.09±4.51pg/ml。添加的AVP的提取回收率约为63%。尿AVP浓度根据患者的水合状态而变化,在尿渗透压小于200mOsm/1时无法检测到,在随意饮水时平均为16.5±7.9pg/ml,禁水12小时后为29.1±7.5pg/ml,禁水36小时后为117.2±13.7pg/ml。

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