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大鼠冠状动脉循环中腺嘌呤核苷酸分解代谢的动力学

Kinetics of adenine nucleotide catabolism in coronary circulation of rats.

作者信息

Fleetwood G, Coade S B, Gordon J L, Pearson J D

机构信息

Section of Vascular Biology, Medical Research Council Clinical Research Centre, Harrow, Middlesex, United Kingdom.

出版信息

Am J Physiol. 1989 Jun;256(6 Pt 2):H1565-72. doi: 10.1152/ajpheart.1989.256.6.H1565.

DOI:10.1152/ajpheart.1989.256.6.H1565
PMID:2544108
Abstract

We have used the rat isolated, perfused heart to study the metabolism of adenine nucleotides on a single passage through the coronary circulation. Low doses (3-30 nmol) of ATP, ADP, or AMP injected as a bolus were extensively catabolized by ectoenzymes. Increasing doses of each nucleotide demonstrated saturability of catabolism that occurred at significantly lower doses of AMP than of ADP or ATP. The patterns of catabolites formed in each case were consistent with the major pathway of metabolism being sequential dephosphorylation of ATP----ADP----AMP----adenosine, although from experiments in which [3H]ATP was co-injected with unlabeled ADP, it appears that some direct conversion of ATP----AMP can occur. Furthermore, particularly in the presence of excess unlabeled ATP, [3H]ADP was phosphorylated to [3H]ATP, indicating that ectoenzymes capable of interconverting nucleotides are present. By evaluating recovery and metabolism in serial samples collected rapidly after bolus injection, we were able to use the integrated form of the Michaelis-Menten equation as developed by Bronikowski et al. (Math. Biosci. 61: 237-266, 1982) to derive Michaelis constant (Km) and maximum velocity times capillary plasma volume (Amax) values for adenosinetriphosphatase, adenosine diphosphatase, and 5'-nucleotidase (450, 300, and 93 microM; and 5.3, 5.9, and 1.7 mumol/min, respectively). This analysis also indicated that there is a high degree of heterogeneity of path lengths within the coronary circulation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们使用大鼠离体灌流心脏来研究腺嘌呤核苷酸在单次通过冠脉循环时的代谢情况。以团注形式注射低剂量(3 - 30纳摩尔)的ATP、ADP或AMP会被胞外酶大量分解代谢。每种核苷酸剂量增加时均显示出分解代谢的饱和性,AMP出现饱和的剂量明显低于ADP或ATP。每种情况下形成的分解代谢产物模式与主要代谢途径一致,即ATP依次脱磷酸生成ADP、AMP、腺苷,不过从[3H]ATP与未标记ADP共同注射的实验来看,似乎存在一些ATP直接转化为AMP的情况。此外,尤其是在存在过量未标记ATP的情况下,[3H]ADP会磷酸化为[3H]ATP,这表明存在能够相互转化核苷酸的胞外酶。通过评估团注注射后快速采集的系列样本中的回收率和代谢情况,我们能够使用Bronikowski等人(《数学生物学》61: 237 - 266, 1982)推导的米氏方程的积分形式来得出三磷酸腺苷酶、二磷酸腺苷酶和5'-核苷酸酶的米氏常数(Km)以及最大速度乘以毛细血管血浆体积(Amax)的值(分别为450、300和93微摩尔;以及5.3、5.9和1.7微摩尔/分钟)。该分析还表明冠脉循环内路径长度存在高度异质性。(摘要截短于250字)

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