Pharmacological characterization of pre- and postsynaptic prostanoid receptors in pig gastric fundus

被引:11
|
作者
De Backer, O [1 ]
Leclere, PG [1 ]
Lefebvre, RA [1 ]
机构
[1] State Univ Ghent, Heymans Inst Pharmacol, Fac Med & Hlth Sci, B-9000 Ghent, Belgium
关键词
prostanoid receptors; acetylcholine release; smooth muscle cells; pig; gastric fundus;
D O I
10.1016/S0028-3908(03)00231-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study characterized the subtype of prostanoid receptors on the cholinergic neurones and smooth muscle cells in circularly oriented muscle strips of the pig gastric fundus. Tissues were electrically stimulated (40 V, 4 Hz, 0.25 ms, 2 min) to induce tritium outflow after incubation with [H-3]-choline. Indomethacin increased the electrically induced tritium outflow, suggesting an inhibitory effect of endogenous prostanoids. In the presence of indomethacin, PGE(2) > PGF(2alpha) > PGI(2) inhibited tritium release while the TP-receptor agonist U-46619 and PGD(2) had no effect. The EP2-receptor agonist butaprost had no effect while the EP1- and EP3-receptor agonist sulprostone mimicked the effect of PGE(2). The effect of sulprostone was not affected by AH 6809, that antagonizes EP1- and EP2-receptors, suggesting the presence of presynaptic EP3-receptors on the cholinergic nerve endings. All prostanoid receptor agonists, except butaprost, contracted the tissues concentration-dependently; the rank order of potency (U-46619 > sulprostone > PGE(2) > PGF(2alpha) > PGD(2) = PGI(2)) suggests the presence of TP- and EP1- and EP3-receptors on the circular smooth muscle cells. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:684 / 690
页数:7
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