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The inhibitory action of two thrombin inhibitors (TI-189 and TI-233) on the contractile responses to 5-hydroxytryptamine and prostaglandin endoperoxide analogue (U-44069) in isolated vascular strips.两种凝血酶抑制剂(TI - 189和TI - 233)对离体血管条对5 - 羟色胺和前列腺素内过氧化物类似物(U - 44069)收缩反应的抑制作用。
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Analysis of the 5-hydroxytryptamine induced contraction of the human basilar arterial strip compared with the rat aortic strip in vitro.体外比较5-羟色胺诱导的人基底动脉条与大鼠主动脉条收缩的分析。
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Endothelium-dependent contractile responses to 5-hydroxytryptamine in the rabbit basilar artery.兔基底动脉对5-羟色胺的内皮依赖性收缩反应。
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The inhibitory effects of N2-dansyl-L-arginine-4-t-butylpiperidine amide (TI233) on contraction of vascular and intestinal smooth muscle.N2-丹磺酰-L-精氨酸-4-叔丁基哌啶酰胺(TI233)对血管和平滑肌收缩的抑制作用。
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本文引用的文献

1
Cumulative dose-response curves. II. Technique for the making of dose-response curves in isolated organs and the evaluation of drug parameters.累积剂量-反应曲线。II. 离体器官中剂量-反应曲线的制作技术及药物参数的评估
Arch Int Pharmacodyn Ther. 1963;143:299-330.
2
A novel series of synthetic thrombin-inhibitors having extremely potent and highly selective action.一系列具有极强且高度选择性作用的新型合成凝血酶抑制剂。
Kobe J Med Sci. 1975 Jun;21(2):43-51.
3
Further evidence for two types of excitatory receptor for 5-hydroxytryptamine in dog vasculature [proceedings].犬血管系统中5-羟色胺两种兴奋性受体的进一步证据[会议论文集]
Br J Pharmacol. 1977 Nov;61(3):466P.
4
Two types of excitatory receptor for 5-hydroxytryptamine in dog vasculature? [proceedings].犬血管系统中5-羟色胺的两种兴奋性受体?[会议论文集]
Br J Pharmacol. 1977 Nov;61(3):465P.

两种凝血酶抑制剂(TI - 189和TI - 233)对离体血管条对5 - 羟色胺和前列腺素内过氧化物类似物(U - 44069)收缩反应的抑制作用。

The inhibitory action of two thrombin inhibitors (TI-189 and TI-233) on the contractile responses to 5-hydroxytryptamine and prostaglandin endoperoxide analogue (U-44069) in isolated vascular strips.

作者信息

Ho W K, Nakao K, Shibata S

出版信息

Br J Pharmacol. 1980;71(2):399-405. doi: 10.1111/j.1476-5381.1980.tb10952.x.

DOI:10.1111/j.1476-5381.1980.tb10952.x
PMID:7225193
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2044436/
Abstract
  1. Two arginine derivatives that were developed as thrombin inhibitors (TI-189 and TI-233) selectively inhibited the 5-hydroxytryptamine (5-HT)-induced contraction of rabbit aortic strips in a competitive manner. The PA2 values of TI-189 and TI-233 were 5.24 +/- 0.21 and 6.23 +/- 0.32 respectively. 2. Even at 10(-4) M they had no inhibitory effect on the contractile response to noradrenaline (NA), histamine, prostaglandin E2 (PGE2), PGF2 alpha, arachidonic acid or potassium in rabbit aortic strips. 3. In dog basilar and coronary arterial strips and also in rat fundus, both agents inhibited the 5-HT response in a non-competitive manner. 4. At 10(-5) M, TI-233 but not TI-189 antagonized effects of NA and KCl in the dog basilar and coronary arteries. 5. These arginine derivatives decreased the contractile responses induced by a prostaglandin endoperoxide analogue (U-44069) in rabbit aorta and in dog basilar and coronary arteries but there was no evidence for competitive antagonism. 6. These results indicate that the arginine derivatives are competitive antagonists selective for 5-HT receptors in rabbit aorta.
摘要
  1. 作为凝血酶抑制剂开发的两种精氨酸衍生物(TI-189和TI-233)以竞争性方式选择性抑制5-羟色胺(5-HT)诱导的兔主动脉条收缩。TI-189和TI-233的PA2值分别为5.24±0.21和6.23±0.32。2. 即使在10^(-4) M浓度下,它们对兔主动脉条对去甲肾上腺素(NA)、组胺、前列腺素E2(PGE2)、前列腺素F2α、花生四烯酸或钾的收缩反应也没有抑制作用。3. 在犬基底动脉和冠状动脉条以及大鼠胃底中,两种药物均以非竞争性方式抑制5-HT反应。4. 在10^(-5) M浓度下,TI-233而非TI-189拮抗犬基底动脉和冠状动脉中NA和KCl的作用。5. 这些精氨酸衍生物降低了前列腺素内过氧化物类似物(U-44069)在兔主动脉以及犬基底动脉和冠状动脉中诱导的收缩反应,但没有竞争性拮抗的证据。6. 这些结果表明,精氨酸衍生物是兔主动脉中5-HT受体的竞争性拮抗剂。