Suppr超能文献

正常受试者和各类疾病患者血清中游离卵泡抑素水平的测定。

Determination of free follistatin levels in sera of normal subjects and patients with various diseases.

作者信息

Sakamoto Y, Shintani Y, Harada K, Abe M, Shitsukawa K, Saito S

机构信息

First Department of Internal Medicine, School of Medicine, University of Tokushima, Japan.

出版信息

Eur J Endocrinol. 1996 Sep;135(3):345-51. doi: 10.1530/eje.0.1350345.

Abstract

We developed an assay system for measuring free follistatin by using an anti-follistatin mouse monoclonal antibody and [125I]activin A. The sensitivity of this assay was 0.5 microgram/l and cross-reactivities with inhibin, luteinizing hormone, follicle-stimulating hormone and growth hormone were all less than 0.5%. The dose-response curves of human sera and follicular fluid were parallel to the standard curve, and the follicular fluid contained a large amount of follistatin (6.4 +/- 0.5 mg/l, mean +/- SEM; N = 13). The within- and between-assay coefficients of variation calculated from the analysis of serum samples of four different concentrations were 3.3-7.8% and 3.9-11.0%, respectively. The recovery rates of free follistatin at five different doses were 86.4 - 102.4%. When activin A was added to the same sample, free follistatin recovery rate declined dose-dependently. Gel filtration analyses of human serum and follicular fluid resulted in a single peak corresponding to authentic follistatin. Using this assay, free follistatin concentrations in sera were measured in normal, pregnant and diseased subjects. The free follistatin level in serum of normal adults was 3.5 +/- 0.2 micrograms/l (N = 60), which was significantly elevated in pregnant women (16.7 +/- 1.3 micrograms/l, N = 56), and in patients with chronic liver disease (8.1 +/- 1.1 micrograms/l, N = 20), chronic renal failure (6.7 +/- 0.9 micrograms/l, N = 42), advanced solid cancer (8.5 +/- 1.0 micrograms/l, N = 39) and hematological malignancies (6.8 +/- 1.0 micrograms/l, N = 18). These data indicated that the free follistatin concentration in serum is detectable and varies during pregnancy and in various diseased states.

摘要

我们利用抗卵泡抑素小鼠单克隆抗体和[125I]激活素A开发了一种用于测量游离卵泡抑素的检测系统。该检测方法的灵敏度为0.5微克/升,与抑制素、黄体生成素、卵泡刺激素和生长激素的交叉反应率均低于0.5%。人血清和卵泡液的剂量反应曲线与标准曲线平行,卵泡液中含有大量卵泡抑素(6.4±0.5毫克/升,平均值±标准误;N = 13)。通过对四种不同浓度血清样本的分析计算得出的批内和批间变异系数分别为3.3 - 7.8%和3.9 - 11.0%。五种不同剂量的游离卵泡抑素回收率为86.4 - 102.4%。当向同一样本中添加激活素A时,游离卵泡抑素回收率呈剂量依赖性下降。对人血清和卵泡液进行凝胶过滤分析得到一个与真实卵泡抑素相对应的单峰。使用该检测方法,对正常、怀孕和患病受试者的血清中游离卵泡抑素浓度进行了测量。正常成年人血清中的游离卵泡抑素水平为3.5±0.2微克/升(N = 60),孕妇(16.7±1.3微克/升,N = 56)、慢性肝病患者(8.1±1.1微克/升,N = 20)、慢性肾衰竭患者(6.7±0.9微克/升,N = 42)、晚期实体癌患者(8.5±1.0微克/升,N = 39)和血液系统恶性肿瘤患者(6.8±1.0微克/升,N = 18)的该水平均显著升高。这些数据表明血清中游离卵泡抑素浓度是可检测的,并且在怀孕期间和各种疾病状态下会发生变化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验