PROSTAGLANDINS AND MYOGENIC CONTROL OF TENSION IN LOWER ESOPHAGEAL SPHINCTER INVITRO

被引:17
作者
DANIEL, EE
CRANKSHAW, J
SARNA, S
机构
[1] MCMASTER UNIV,DEPT SURG,HAMILTON L8S 4J9,ONTARIO,CANADA
[2] MCMASTER UNIV,DEPT ELECT BIOENGN,HAMILTON L8S 4J9,ONTARIO,CANADA
来源
PROSTAGLANDINS | 1979年 / 17卷 / 04期
基金
英国医学研究理事会;
关键词
Endoperoxides; Esophageal Body; Lower Esophageal Sphincter; Prostaglandin Receptors;
D O I
10.1016/0090-6980(79)90014-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Active tension is produced by the lower esophageal sphincter (LES) of North American opossum in vitro by a myogenic mechanism. Strips of LES, but not those from the esophageal body, contracted to prostaglandin (PG)F2α, stable expoxymethano derivatives of PGH2 and to thromboxane B2. Stable endoperoxides were more than 500 times more potent than PGF2α. PGI2 and 6-keto PGF1α were weak relaxants of LES strips. LES strips transformed arachidonic acid into contractile substances. This transformation was prevented by agents which interfere with PG synthesis by inhibiting cyclo-oxygenase [indomethacin (IDM), 5,8,11,14-eicosatetraynoic acid (ETA) or thromboxane synthetase [imidazole]. Tranylcypromine 500 μg/ml also inhibited contractions to arachidonic acid. These agents also reduced muscle tone, so that endogenous PG formation may contribute to active tension in the LES. ETA and IDM increased tone before inhibiting it, and this effect was prevented by prior treatment with ETA or imidazole. There may also be an endogenous PG which inhibits LES tone. The possibility that this may be PGI2 is discussed. © 1979.
引用
收藏
页码:629 / 639
页数:11
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