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一种使用荧光底物的改良淀粉酶测定法及其在大鼠腮腺体外研究中的应用。

A modified amylase assay, using a fluorescent substrate, and its application to a study of the rat parotid gland in vitro.

作者信息

Owen D G, Jordan C C

出版信息

J Pharmacol Methods. 1981 Dec;6(4):281-93. doi: 10.1016/0160-5402(81)90068-1.

Abstract

A modified fluorescence assay for alpha-amylase activity is described. The method employs amylopectin anthranilate as substrate and offers the advantages of economy of time and resources over a previously described technique using the same substrate. The sample containing alpha-amylase is incubated with the substrate for 5 min at 30 degree C in a final volume of 750 microliter. The fluorescent products of the reaction are separated from the substrate by the addition of methanol, and the methanol-soluble fluorescence is measured in a fluorescence spectrometer. A highly reproducible linear relationship between fluorescence and alpha-amylase activity is obtained for enzyme activities up to 2 units. The absolute sensitivity of the assay under these conditions was estimated to be 0.02 EU (= 0.08 EU ml-1). The application of the assay method to a study of the effects of isoprenaline and substance P-like peptides on the release of alpha-amylase from rat parotid gland slices is described. The assay is particularly suitable for studies on agonists, such as substance P, which have a low ceiling effect in terms of amylase release.

摘要

本文描述了一种改良的α-淀粉酶活性荧光测定法。该方法采用支链淀粉邻氨基苯甲酸酯作为底物,与先前使用相同底物的技术相比,具有节省时间和资源的优点。将含有α-淀粉酶的样品与底物在30℃下孵育5分钟,最终体积为750微升。通过加入甲醇将反应的荧光产物与底物分离,并在荧光光谱仪中测量甲醇可溶性荧光。对于高达2个单位的酶活性,荧光与α-淀粉酶活性之间获得了高度可重复的线性关系。在这些条件下,该测定法的绝对灵敏度估计为0.02 EU(= 0.08 EU ml-1)。本文描述了该测定方法在研究异丙肾上腺素和P物质样肽对大鼠腮腺切片中α-淀粉酶释放的影响方面的应用。该测定法特别适用于对激动剂(如P物质)的研究,这些激动剂在淀粉酶释放方面具有较低的上限效应。

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Synergistic interactions between forskolin, isoprenaline and substance P as secretagogues in rat parotid glands.
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