Ito S, Okuda E, Sugama K, Negishi M, Hayaishi O
Department of Cell Biology, Osaka Bioscience Institute, Suita, Japan.
Br J Pharmacol. 1990 Jan;99(1):13-4. doi: 10.1111/j.1476-5381.1990.tb14645.x.
ZK110841 and AH6809, an agonist and an antagonist of prostaglandin DP-receptors on human platelets, were evaluated with a fibroblastic cell line from bovine embryonic trachea (EBTr) which specifically responds to prostaglandin D2 (PGD2). ZK110841, equipotent to PGD2, elevated the adenosine 3':5'-cyclic monophosphate (cyclic AMP) level in EBTr cells dose-dependently, being more than 100 fold over the basal level at 1 microM. The half-maximally effective concentration of PGD2 or ZK110841 was 10-30 nM. Increasing concentrations (10(-7)-10(-4) M) of AH6809 (which possesses negligible intrinsic agonist activity) produced parallel shifts to the right of dose-response curves to PGD2 and ZK110841. Schild plots of these data were linear (correlation close to unity) and pA2 values against PGD2 and ZK110841 were calculated to be 6.36 and 6.57, respectively, indicating that AH6809 is a simple and competitive antagonist. These results demonstrate that ZK110841, AH6809 and EBTr cells will be useful for characterization of DP-receptors.
ZK110841和AH6809分别是人类血小板上前列腺素DP受体的激动剂和拮抗剂,利用来自牛胚胎气管(EBTr)的成纤维细胞系对其进行了评估,该细胞系对前列腺素D2(PGD2)有特异性反应。ZK110841与PGD2等效,能剂量依赖性地提高EBTr细胞中3':5'-环磷酸腺苷(环磷腺苷)水平,在1微摩尔时比基础水平高出100多倍。PGD2或ZK110841的半数最大效应浓度为10 - 30纳摩尔。AH6809(内在激动剂活性可忽略不计)浓度增加(10(-7)-10(-4) 摩尔)会使PGD2和ZK110841的剂量反应曲线平行右移。这些数据的Schild图呈线性(相关性接近1),针对PGD2和ZK110841计算出的pA2值分别为6.36和6.57,表明AH6809是一种简单的竞争性拮抗剂。这些结果表明,ZK110841、AH6809和EBTr细胞将有助于DP受体的特性研究。