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首页> 外文期刊>Steroids: An International Journal >Development of a highly sensitive ELISA for aldosterone in mouse urine: Validation in physiological and pathophysiological states of aldosterone excess and depletion.
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Development of a highly sensitive ELISA for aldosterone in mouse urine: Validation in physiological and pathophysiological states of aldosterone excess and depletion.

机译:小鼠尿中醛固酮高灵敏度ELISA的开发:醛固酮过量和耗竭的生理和病理生理状态验证。

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BACKGROUND: Clinical studies have established aldosterone as a critical physiological and pathophysiological factor in salt and water homeostasis, blood pressure control and in heart failure. Genetic and physiological studies of mice are used to model these processes. A sensitive and specific assay for aldosterone is therefore needed to monitor adrenocortical activity in murine studies of renal function and cardiovascular diseases. METHODS: Antibodies against aldosterone were raised in sheep as previously described. HRP-Donkey-anti-sheep IgG enzyme tracer was produced in our laboratory using the Lightning-Link HRP technique. Aldosterone ELISA protocol was validated and optimised to achieve the best sensitivity. The assay was validated by analysing the urine of mice collected under various experimental conditions designed to stimulate or suppress aldosterone in the presence of other potentially interfering steroid hormones. RESULTS: Cross-reactivity with the steroids most likely to interfere was minimal: corticosterone=0.0028%, cortisol=0.0006%, DOC=0.0048% except for 5alpha-dihydro-aldosterone=1.65%. Minimum detection limit of this ELISA was 5.2pmole/L (1.5pg/mL). The validity of urinary aldosterone ELISA was confirmed by the excellent correlation between results obtained before and after solvent extraction and HPLC separation step (Y=1.092X+0.03, R(2)=0.995, n=54). Accuracy studies, parallelism and imprecision data were determined and all found to be satisfactory. Using this assay, mean urinary aldosterone levels were (i) approximately 60-fold higher in females than males mice; (ii) increased 6-fold by dietary sodium restriction; (iii) increased 10-fold by ACTH infusion and (iv) reduced by >60% in Cyp11b1 null mice. CONCLUSION: We describe an ELISA for urinary aldosterone that is suitable for repeated non-invasive measurements in mice. Female aldosterone levels are higher than males. Unlike humans, most aldosterone in mouse urine is not conjugated. Increased levels were noted in response to dietarysodium restriction and ACTH treatment. The sensitivity of the assay is sufficient to detect suppressed levels in mouse models of congenital adrenal hyperplasia.
机译:背景:临床研究已将醛固酮确立为盐和水稳态,血压控制和心力衰竭的关键生理和病理生理因素。小鼠的遗传和生理研究用于模拟这些过程。因此,在肾脏功能和心血管疾病的鼠类研究中,需要一种灵敏且特异性的醛固酮测定法来监测肾上腺皮质活动。方法:如前所述,在绵羊中产生了针对醛固酮的抗体。 HRP-驴抗绵羊IgG酶示踪剂是在我们的实验室中使用Lightning-Link HRP技术生产的。醛固酮ELISA方案经过验证和优化,以实现最佳灵敏度。该分析通过分析在各种实验条件下收集的小鼠尿液来验证,该实验条件设计为在存在其他潜在干扰类固醇激素的情况下刺激或抑制醛固酮。结果:与最可能干扰的类固醇的交叉反应极少:除了5α-二氢-醛固酮= 1.65%外,皮质酮= 0.0028%,皮质醇= 0.006%,DOC = 0.0048%。该ELISA的最低检测限为5.2pmole / L(1.5pg / mL)。尿醛固酮ELISA的有效性通过溶剂提取前后的结果与HPLC分离步骤之间的良好相关性得到证实(Y = 1.092X + 0.03,R(2)= 0.995,n = 54)。确定了准确性研究,并行度和不精确度数据,都令人满意。使用该试验,平均尿醛固酮水平(i)雌性小鼠的雄性醛固酮水平比雄性小鼠高约60倍; (ii)通过饮食中的钠限制增加了6倍; (iii)通过ACTH输注增加了10倍,并且(iv)在Cyp11b1空小鼠中减少了> 60%。结论:我们描述了尿醛固酮的酶联免疫吸附测定法,适用于在小鼠中重复进行非侵入性测量。女性醛固酮水平高于男性。与人类不同,小鼠尿液中的大多数醛固酮不缀合。注意到对饮食中的钠限制和ACTH治疗后,其水平增加了。该测定法的灵敏度足以检测先天性肾上腺增生的小鼠模型中抑制水平。

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