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血浆精氨酸加压素放射免疫分析法的建立及其在中枢性尿崩症患儿诊断中的应用

[Development of radioimmunoassay for plasma arginine vasopressin and its application to the diagnosis of children with central diabetes insipidus].

作者信息

Kato T

出版信息

Hokkaido Igaku Zasshi. 1986 Mar;61(2):303-13.

PMID:3721401
Abstract

For measurement of plasma arginine vasopressin (AVP) in children with central diabetes insipidus (DI), a sensitive and specific radioimmunoassay (RIA) for AVP was developed. The anti AVP serum used in this assay bound 50 percent of an purified 125-I-labeled-AVP (125I-AVP) at a final dilution of 5 X 10(4) and its cross reaction with lysine vasopressin, 1-deamino-8-D-arginine vasopressin and oxytocin were 7, 15, and 0%, respectively. Column chromatography of Sephadex G-25 superfine was used for purification of 125I-AVP and four major peaks of radioactivity were observed. The purified 125I-AVP was found in 3rd peak by the highest binding activity with the anti-AVP serum. On the other hand, extraction of AVP from plasma was carried out by the acetone extraction procedure and as little as 1.2 pg per milliliter of AVP in plasma was detected in this RIA. In dehydration state plasma concentration of AVP was 4.5 +/- 1.1 pg/ml (mean +/- SE) in normal seven children (control), 1.5 +/- 0.2 pg/ml in six patients with complete DI and 3.4 +/- 0.6 pg/ml in five patients with partial DI diagnosed with Miller test (complete DI vs partial DI; p less than 0.02, partial DI vs control; no significant). The evaluation of diagnostic value of AVP level measured with RIA in complete DI and partial DI diagnosed with Miller test based on urine osmolality was discussed.

摘要

为了测量中枢性尿崩症(DI)患儿的血浆精氨酸血管加压素(AVP),开发了一种灵敏且特异的AVP放射免疫测定法(RIA)。该测定法中使用的抗AVP血清在终浓度为5×10⁴时能结合50%的纯化¹²⁵I标记的AVP(¹²⁵I - AVP),其与赖氨酸加压素、1 - 去氨基 - 8 - D - 精氨酸加压素和催产素的交叉反应分别为7%、15%和0%。使用Sephadex G - 25超细柱色谱法纯化¹²⁵I - AVP,观察到四个主要放射性峰。通过与抗AVP血清的最高结合活性,在第三个峰中发现了纯化的¹²⁵I - AVP。另一方面,采用丙酮萃取法从血浆中提取AVP,在此RIA中可检测到低至每毫升血浆1.2皮克的AVP。在脱水状态下,7名正常儿童(对照组)的血浆AVP浓度为4.5±1.1皮克/毫升(均值±标准误),6名完全性DI患者为1.5±0.2皮克/毫升,5名经米勒试验诊断为部分性DI的患者为3.4±0.6皮克/毫升(完全性DI与部分性DI比较;p<0.02,部分性DI与对照组比较;无显著差异)。讨论了基于尿渗透压用RIA测量的AVP水平在经米勒试验诊断的完全性DI和部分性DI中的诊断价值评估。

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