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Hoe 140对激肽作用于上皮细胞的拮抗作用:明显的竞争性和非竞争性相互作用。

Antagonism of kinin effects on epithelial by Hoe 140: apparently competitive and non-competitive interactions.

作者信息

Cuthbert A W, MacVinish L J, Pickles R J

机构信息

Department of Pharmacology, University of Cambridge.

出版信息

Br J Pharmacol. 1992 Nov;107(3):797-802. doi: 10.1111/j.1476-5381.1992.tb14526.x.

Abstract
  1. Hoe-140, a potent kinin receptor antagonist, was investigated for its ability to inhibit the effects of lysylbradykinin (kallidin) on a cultured colonic epithelium, HCA-7 Colony 29, derived from a human adenocarcinoma. 2. Measurements of electrogenic chloride secretion (as short circuit current), and of intracellular Ca2+ (from Fura-2 fluorescence) were used to assess the action of lysylbradykinin in the absence and presence of Hoe 140. 3. From short circuit current data, Hoe 140 appeared to be a competitive antagonist with a Ki value of 5 nM. However, with measurements of intracellular Ca2+ Hoe 140 was apparently a non-competitive antagonist with a Ki of between 4-6 nM. 4. Because of the unexpected finding of non-competitive antagonism, measurements were made with a second antagonist pair, histamine and mepyramine. Mepyramine behaved as a competitive antagonist against responses to histamine with a Ki value of approximately 5 nM when short circuit current measurements were evaluated. However, when intracellular Ca2+ concentration was used as a measure mepyramine, 30 nM, produced a near parallel shift in the response curve, but at 100 nM the maximal response was depressed. 5. The reasons why the apparent type of antagonism depends upon the method of measurement is discussed, bearing in mind that the increase in intracellular Ca2+ is a signal which precedes the increase in short circuit current.
摘要
  1. 强效激肽受体拮抗剂Hoe - 140,被研究其抑制赖氨酰缓激肽(胰激肽)对源自人腺癌的培养结肠上皮HCA - 7克隆29的作用的能力。2. 测量电致氯分泌(作为短路电流)以及细胞内Ca2 +(通过Fura - 2荧光),用于评估在不存在和存在Hoe 140的情况下赖氨酰缓激肽的作用。3. 根据短路电流数据,Hoe 140似乎是一种竞争性拮抗剂,Ki值为5 nM。然而,通过测量细胞内Ca2 +时,Hoe 140显然是一种非竞争性拮抗剂,Ki值在4 - 6 nM之间。4. 由于意外发现非竞争性拮抗作用,使用了第二对抗拮抗剂组胺和甲氧苄胺进行测量。当评估短路电流测量时,甲氧苄胺对组胺反应表现为竞争性拮抗剂,Ki值约为5 nM。然而,当使用细胞内Ca2 +浓度作为测量指标时,30 nM的甲氧苄胺使反应曲线产生近乎平行的移动,但在100 nM时最大反应受到抑制。5. 考虑到细胞内Ca2 +的增加是短路电流增加之前的一个信号,讨论了拮抗作用的明显类型为何取决于测量方法的原因。

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Adv Exp Med Biol. 1989;247A:105-11. doi: 10.1007/978-1-4615-9543-4_15.

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