Hellewell P G, Pearson J D
Circ Res. 1983 Jul;53(1):1-7. doi: 10.1161/01.res.53.1.1.
Adenosine uptake was studied in the piglet isolated perfused lung by means of the single-circulation paired-tracer dilution technique. Adenosine was efficiently taken up from the pulmonary vascular bed, and the process was potently inhibited by dipyridamole. Following uptake, adenosine was incorporated into intracellular nucleotides, and at low perfusate concentrations, little or none of the incorporated radioactivity returned to the circulation. At higher concentrations, cellular uptake was saturable and products of intracellular catabolism (inosine and hypoxanthine) were returned to the circulation. Perfusion of low concentrations of adenosine after inhibition of pulmonary adenosine kinase led to a proportional decrease in the retention of nucleotides and to a release of inosine and hypoxanthine. A small proportion of adenosine was metabolised extracellularly by adenosine deaminase; this activity was not released from perfused lungs and is apparently an ecto-enzyme.
采用单循环双示踪剂稀释技术,在仔猪离体灌注肺中研究了腺苷摄取情况。腺苷可从肺血管床有效摄取,且该过程受到双嘧达莫的强烈抑制。摄取后,腺苷被整合到细胞内核苷酸中,在灌注液浓度较低时,整合的放射性很少或没有返回循环。在较高浓度时,细胞摄取具有饱和性,细胞内分解代谢产物(肌苷和次黄嘌呤)返回循环。抑制肺腺苷激酶后灌注低浓度腺苷,导致核苷酸保留量成比例下降,并释放出肌苷和次黄嘌呤。一小部分腺苷在细胞外被腺苷脱氨酶代谢;这种活性不会从灌注肺中释放出来,显然是一种外酶。