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血浆肾素活性的放射免疫测定

Radioimmunoassay of plasma renin activity.

作者信息

Sealey J E, Laragh J H

出版信息

Semin Nucl Med. 1975 Apr;5(2):189-202. doi: 10.1016/s0001-2998(75)80033-x.

Abstract

Plasma renin activity is quantitated by measuring the rate of angiotensin generation during incubation of plasma renin with endogenous renin substrate. The angiotensin is quantitated by radioimmunoassay. Our studies indicate that the incubation step is best carried out in undiluted plasma at the pH optimum for renin (pH 5.7) in the presence of EDTA, neomycin, and DFP or PMSF. By using these conditions, incubation of low-renin samples can be prolonged for up to 18 hr, because angiotensinases and converting enzyme are completely inhibited. Accuracy is enhanced by prolongation of the incubation time, which results in more angiotensin and eliminates the need for blank subtraction. Incubation at pH 7.4 is disadvantageous because of lower rates of generation of angiotensin 1, because of the inability to maintain pH constant without addition of strong buffer, and because the incubation step cannot be prolonged beyond 3 hr. Dilution of plasma is undesirable because it results in a slower reaction rate due to dilution of both enzyme and substrate, and it is not possible to correct for the effect of substrate dilution. The radioimmunoassay of angiotensin I presents few unusual problems. The volume of plasma assayed should be 20 muI or less. If blank subtraction is used, antibodies should be screened to determine the extent to which they bind nonspecific substances in plasma, and then to ascertain whether the blank is entirely additive when angiotensin is added to it. Assay sensitivity is an important issue, since approximately 30 percent of patients with essential hypertension have subnormal plasma renin activity. In a study of three different commercial kits we found that many low-renin samples were undetectable and major fractions could not be discriminated with precision or consistency from normal renin samples. However, the incubation conditions can be easily modified, so that an 18-hr incubation can be utilized and then low-renin samples can be detected with the same degree of accuracy as those with normal plasma renin activity.

摘要

通过在血浆肾素与内源性肾素底物孵育期间测量血管紧张素生成速率来定量血浆肾素活性。血管紧张素通过放射免疫测定法定量。我们的研究表明,孵育步骤最好在未稀释的血浆中于肾素的最适pH(pH 5.7)下,在存在乙二胺四乙酸(EDTA)、新霉素以及二异丙基氟磷酸(DFP)或苯甲基磺酰氟(PMSF)的情况下进行。通过使用这些条件,低肾素样本的孵育时间可延长至18小时,因为血管紧张素酶和转化酶被完全抑制。孵育时间的延长提高了准确性,这会产生更多的血管紧张素并消除了空白扣除的需要。在pH 7.4下孵育是不利的,因为血管紧张素1的生成速率较低,因为在不添加强缓冲剂的情况下无法维持pH恒定,并且因为孵育步骤不能延长超过3小时。血浆稀释是不可取的,因为这会由于酶和底物的稀释导致反应速率变慢,并且无法校正底物稀释的影响。血管紧张素I的放射免疫测定没有什么特别的问题。所测定的血浆体积应在20微升或更少。如果使用空白扣除,应筛选抗体以确定它们与血浆中非特异性物质结合的程度,然后确定当向其中添加血管紧张素时空白是否完全是累加性的。测定灵敏度是一个重要问题,因为大约30%的原发性高血压患者血浆肾素活性低于正常水平。在对三种不同商业试剂盒的研究中,我们发现许多低肾素样本无法检测到,并且主要部分无法与正常肾素样本精确或一致地区分。然而,孵育条件可以很容易地改变,这样就可以利用18小时的孵育,然后以与正常血浆肾素活性样本相同的准确度检测低肾素样本。

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