Cheng J, Hong S L
Institute of Basic Medical Sciences, Beijing.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1992 Oct;14(5):351-6.
This paper details the methods of establishing stock culture and subculture of calf and pig aorta endothelial cells and the effects of bradykinin, ionophore A23187, trypsin and arachidonic acid (AA) on the release of prostacyclin (PGI2) from the cells. The release was measured by 6-keto PGF1 alpha radioimmunoassay. The results showed that the stimuli significantly increased the release of PGI2 in the two endothelial cell types (P < 0.01, n = 8), and the release was much stronger in pig than in calf endothelial cells under the experimental conditions. We therefore suggest that the reactivities of the two endothelial cells to the stimuli differ. The results offer useful information for further research of the mechanism of their pharmacologic actions on endothelial cells and their relationship with PGI2.
本文详述了小牛和猪主动脉内皮细胞原代培养及传代培养的方法,以及缓激肽、离子载体A23187、胰蛋白酶和花生四烯酸(AA)对这些细胞释放前列环素(PGI2)的影响。通过6-酮-前列腺素F1α放射免疫分析法测定释放量。结果表明,这些刺激物显著增加了两种内皮细胞类型中PGI2的释放(P<0.01,n=8),并且在实验条件下,猪内皮细胞中的释放比小牛内皮细胞中的释放要强得多。因此,我们认为这两种内皮细胞对刺激物的反应性不同。这些结果为进一步研究它们对内皮细胞的药理作用机制及其与PGI2的关系提供了有用的信息。