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[采用新型放射免疫分析系统对非孕妇和孕妇体内17α,20α-二羟基-4-孕烯-3-酮的研究]

[Studies on 17 alpha, 20 alpha-dihydroxy-4-pregnen-3-one in non-pregnant and pregnant women by a new radioimmunoassay system].

作者信息

Satoh K

出版信息

Nihon Naibunpi Gakkai Zasshi. 1987 Mar 20;63(3):227-38. doi: 10.1507/endocrine1927.63.3_227.

Abstract

17 alpha, 20 alpha-dihydroxy-4-pregnen-3-one (17 alpha, 20 alpha-P) is reportedly a hyper-tensinogenic substance in a model of ACTH induced hypertension in sheep (Scoggins et al). This steroid has not previously been measured in Japan. We have developed a new radioimmunoassay (RIA) system for 17 alpha, 20 alpha-P, and measured this steroid in peripheral blood samples from non-pregnant and pregnant women. In this clinical investigation concentrations of 17 alpha-hydroxyprogesterone (17 alpha-OHP) and progesterone (P) were also measured in the same clinical samples. Specific anti-serum against 17 alpha, 20 alpha-P-3-carboxymethyloxime-BSA was generated in rabbits. Cross-reactions with 5-pregnen-3 beta, 17 alpha 20 alpha-triol (17 alpha, 20 alpha-P5) and 17 alpha-OHP were 42 and 2.4%, respectively. Other steroids showed cross-reactivity of less than 1%. As an internal standard dexamethasone (500 ng/100 microliter) was added to the samples which were extracted twice with 6 volumes of dichloromethane. Separation of the plasma extract was performed by high performance liquid chromatography (HPLC) with the ODS column in the solvent system, acetonitrile:water = 55:45. Eluates of the 17 alpha, 20 alpha-P and 17 alpha-OHP fractions were collected separately and the solvent was evaporated in vacuo. RIA was carried out on each extract with specific anti-sera. RIA of P was performed independently using the anti-P-3-CMO-BSA antiserum; 0.1 ml of serum was extracted with n-hexane and subjected to RIA without chromatography. The coefficient of variation for intra- and interassay (n = 10) were 8.5 and 11.7% for 17 alpha, 20 alpha-P; 7.2 and 12.1% for 17-OHP and 10.5 and 14.0% for P, respectively. The recovery rates of 17 alpha, 20 alpha-P, 17 alpha-OHP and P were 95 +/- 1.5, 93.2 +/- 3.5 and 97.5 +/- 4.2%, respectively. With the use of this method, 17 alpha, 20 alpha-P was measured in the blood samples from the menstrual cycle and normal pregnancy. The mean serum 17 alpha, 20 alpha-P concentrations +/- SD in the follicular, ovulatory and luteal phases, and in the first, second and third trimesters were; 76 +/- 6.0, 100 +/- 31, 101 +/- 6.4, 226 +/- 80, 151 +/- 48 and 367 +/- 99 pg/ml, respectively.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

据报道,17α,20α-二羟基-4-孕烯-3-酮(17α,20α-P)在绵羊促肾上腺皮质激素诱导的高血压模型中是一种致高血压物质(斯科金斯等人)。此前日本尚未对这种类固醇进行过测量。我们开发了一种针对17α,20α-P的新型放射免疫分析(RIA)系统,并对非孕妇和孕妇的外周血样本中的这种类固醇进行了测量。在这项临床研究中,还在相同的临床样本中测量了17α-羟孕酮(17α-OHP)和孕酮(P)的浓度。用兔子制备了针对17α,20α-P-3-羧甲基肟-BSA的特异性抗血清。与5-孕烯-3β,17α,20α-三醇(17α,20α-P5)和17α-OHP的交叉反应分别为42%和2.4%。其他类固醇的交叉反应率低于1%。作为内标,将地塞米松(500 ng/100微升)加入样本中,样本用6倍体积的二氯甲烷萃取两次。血浆提取物通过高效液相色谱(HPLC)在乙腈:水 = 55:45的溶剂系统中使用ODS柱进行分离。分别收集17α,20α-P和17α-OHP馏分的洗脱液,并在真空中蒸发溶剂。用特异性抗血清对每个提取物进行放射免疫分析。使用抗P-3-CMO-BSA抗血清独立进行P的放射免疫分析;0.1毫升血清用正己烷萃取,不经色谱直接进行放射免疫分析。17α,20α-P的批内和批间变异系数(n = 10)分别为8.5%和11.7%;17-OHP的批内和批间变异系数分别为7.2%和12.1%;P的批内和批间变异系数分别为10.5%和14.0%。17α,20α-P、17α-OHP和P的回收率分别为95±1.5%、93.2±3.5%和97.5±4.2%。使用该方法,对月经周期和正常妊娠的血样中的17α,20α-P进行了测量。卵泡期、排卵期和黄体期以及妊娠第一、第二和第三个月的血清17α,20α-P平均浓度±标准差分别为:76±6.0、100±31、101±6.4、226±80、151±48和367±99 pg/ml。(摘要截短于400字)

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