EVALUATION OF ZK110841 AND AH6809, AN AGONIST AND AN ANTAGONIST OF PROSTAGLANDIN DP-RECEPTORS ON HUMAN-PLATELETS, WITH A PGD2-RESPONSIVE CELL-LINE FROM BOVINE EMBRYONIC TRACHEA

被引:29
作者
ITO, S
OKUDA, E
SUGAMA, K
NEGISHI, M
HAYAISHI, O
机构
关键词
D O I
10.1111/j.1476-5381.1990.tb14645.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 μM. 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.
引用
收藏
页码:13 / 14
页数:2
相关论文
共 11 条
[1]   SOME QUANTITATIVE USES OF DRUG ANTAGONISTS [J].
ARUNLAKSHANA, O ;
SCHILD, HO .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01) :48-58
[2]   HETEROCYCLIC PROSTAGLANDIN ANALOGS .3. THE RELATIONSHIP OF CONFIGURATION TO BIOLOGICAL-ACTIVITY FOR SOME HYDANTOIN PROSTAGLANDIN ANALOGS [J].
BROCKWELL, MA ;
CALDWELL, AG ;
WHITTAKER, N ;
BEGLEY, MJ .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1981, (03) :706-711
[3]  
COLEMAN R A, 1985, British Journal of Pharmacology, V85, p273P
[4]   THE CLASSIFICATION OF PROSTAGLANDIN DP-RECEPTORS IN PLATELETS AND VASCULATURE USING BW-A868C, A NOVEL, SELECTIVE AND POTENT COMPETITIVE ANTAGONIST [J].
GILES, H ;
LEFF, P ;
BOLOFO, ML ;
KELLY, MG ;
ROBERTSON, AD .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 96 (02) :291-300
[5]   PROSTAGLANDIN-D2 INTERACTS AT THROMBOXANE RECEPTOR-SITES ON GUINEA-PIG PLATELETS [J].
HAMIDBLOOMFIELD, S ;
WHITTLE, BJR .
BRITISH JOURNAL OF PHARMACOLOGY, 1986, 88 (04) :931-936
[6]   PROSTAGLANDIN-D2 - A BIOCHEMICAL PERSPECTIVE [J].
ITO, S ;
NARUMIYA, S ;
HAYAISHI, O .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1989, 37 (04) :219-234
[7]   AH6809, A PROSTAGLANDIN DP-RECEPTOR BLOCKING DRUG ON HUMAN-PLATELETS [J].
KEERY, RJ ;
LUMLEY, P .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 94 (03) :745-754
[8]   STUDIES ON THE CHARACTERIZATION OF PROSTANOID RECEPTORS - A PROPOSED CLASSIFICATION [J].
KENNEDY, I ;
COLEMAN, RA ;
HUMPHREY, PPA ;
LEVY, GP ;
LUMLEY, P .
PROSTAGLANDINS, 1982, 24 (05) :667-689
[9]  
ROBERTSON RP, 1986, PROSTAG OTH LIPID M, V31, P395
[10]   STIMULATION OF CAMP FORMATION BY PROSTAGLANDIN-D2 IN PRIMARY CULTURES OF BOVINE ADRENAL-MEDULLARY CELLS - IDENTIFICATION OF THE RESPONSIVE POPULATION AS FIBROBLASTS [J].
SUGAMA, K ;
TANAKA, T ;
YOKOHAMA, H ;
NEGISHI, M ;
HAYASHI, H ;
ITO, S ;
HAYAISHI, O .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1011 (01) :75-80