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利用选择性拮抗剂CI-988、L-365,260和地伐西匹对豚鼠胃新平滑肌制剂中的胆囊收缩素受体进行表征。

Characterization of CCK receptors in a novel smooth muscle preparation from the guinea-pig stomach by use of the selective antagonists CI-988, L-365,260 and devazepide.

作者信息

Boyle S J, Tang K W, Woodruff G N, McKnight A T

机构信息

Parke-Davis Neuroscience Research Centre, Addenbrookes Hospital Site, Cambridge.

出版信息

Br J Pharmacol. 1993 Aug;109(4):913-7. doi: 10.1111/j.1476-5381.1993.tb13707.x.

DOI:10.1111/j.1476-5381.1993.tb13707.x
PMID:8401944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2175762/
Abstract
  1. The cholecystokinin receptors mediating motor responses in a novel smooth muscle preparation from the corpus region of the guinea-pig stomach have been characterized by use of five agonist peptides and the antagonists CI-988, L-365,260 and devazepide. 2. Mucosa-denuded strips of circular muscle were contracted in a concentration-dependent manner by the five cholecystokinin (CCK)-related peptides CCK-8S, pentagastrin, gastrin-I, CCK-8US and CCK-4. 3. CI-988 was a powerful antagonist of the response to pentagastrin with an affinity (pKB = 9.49) similar to that obtained in CCKB receptor binding assays. With CCK-8S as the agonist, CI-988 was approximately 1000 fold less powerful as an antagonist. 4. Devazepide powerfully blocked responses to CCK-8S with an affinity (pKB = 9.54) that was in agreement with reported functional data obtained in pancreatic amylase secretion studies, a system exhibiting CCKA receptor activity. Devazepide displayed lower affinity against pentagastrin than against CCK-8S. 5. CI-988 blocked responses to pentagastrin in an insurmountable manner in the presence of 3 nM devazepide; a concentration previously shown to block the CCKA receptor. The nature of the antagonism observed with L-365,260 was unaltered by the presence of devazepide. 6. The guinea-pig stomach corpus smooth muscle preparation contains both subtypes of CCK receptor and will be useful as a pharmacological tool for investigating the functional effects of novel CCK ligands.
摘要
  1. 通过使用五种激动剂肽以及拮抗剂CI - 988、L - 365,260和地伐西匹,对豚鼠胃体部一种新型平滑肌制剂中介导运动反应的胆囊收缩素受体进行了特性研究。2. 五种胆囊收缩素(CCK)相关肽CCK - 8S、五肽胃泌素、胃泌素 - I、CCK - 8US和CCK - 4使去黏膜的环行肌条呈浓度依赖性收缩。3. CI - 988是对五肽胃泌素反应的强效拮抗剂,其亲和力(pKB = 9.49)与在CCKB受体结合试验中获得的相似。以CCK - 8S作为激动剂时,CI - 988作为拮抗剂的效力约低1000倍。4. 地伐西匹强效阻断对CCK - 8S的反应,其亲和力(pKB = 9.54)与在胰腺淀粉酶分泌研究中获得的报道功能数据一致,该系统表现出CCKA受体活性。地伐西匹对五肽胃泌素的亲和力低于对CCK - 8S的亲和力。5. 在存在3 nM地伐西匹(先前已证明该浓度可阻断CCKA受体)的情况下,CI - 988以不可克服的方式阻断对五肽胃泌素的反应;L - 365,260所观察到的拮抗性质不受地伐西匹存在的影响。6. 豚鼠胃体平滑肌制剂含有两种CCK受体亚型,将作为研究新型CCK配体功能作用的药理学工具。

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Characterization of CCK receptors in a novel smooth muscle preparation from the guinea-pig stomach by use of the selective antagonists CI-988, L-365,260 and devazepide.利用选择性拮抗剂CI-988、L-365,260和地伐西匹对豚鼠胃新平滑肌制剂中的胆囊收缩素受体进行表征。
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Am J Physiol. 1989 Jul;257(1 Pt 1):G169-74. doi: 10.1152/ajpgi.1989.257.1.G169.
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Combined dose-ratio analysis of cholecystokinin receptor antagonists, devazepide, lorglumide and loxiglumide in the guinea-pig gall bladder.豚鼠胆囊中胆囊收缩素受体拮抗剂、地伐西匹、洛谷胺和洛昔谷胺的联合剂量比分析
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3
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本文引用的文献

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Some quantitative uses of drug antagonists.药物拮抗剂的一些定量应用。
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Effects of benzodiazepines on responses of guinea-pig ileum and gall-bladder and rat pancreatic acini to cholecystokinin.苯二氮䓬类药物对豚鼠回肠和胆囊以及大鼠胰腺腺泡对胆囊收缩素反应的影响。
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