首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Characterization of interactions between local anesthetics and histamine H-1 receptor by cell membrane chromatography model
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Characterization of interactions between local anesthetics and histamine H-1 receptor by cell membrane chromatography model

机译:细胞膜色谱模型局部麻醉剂与组胺H-1受体相互作用的表征

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摘要

Local anesthetic has a wide application in clinical practice. However, angioedema, an adverse reaction caused by local anesthetics, has been reported to be related to histamine H-1 receptor (H1R). Hence, an effective and practical method for investigating the interaction characteristics between local anesthetics and H1R is needed. In this work, the competition binding assay and the relative standard method based on H1R-HEK293/cell membrane chromatography (CMC) were developed to analyze the equilibrium dissociation constant (K-D) values of local anesthetics with H1R. The activity of drugs toward H1R was evaluated by intracellular Ca2+ imaging assay. Molecular docking was used to verify the interaction modes that occurred at the activate pocket of H1R protein. Results showed that the local anesthetics can directly occupy histamine binding sites on H1R, and the K-D values obtained from different CMC methods exhibited positive correlations with each other (p < 0.01). The K-D values of tetracaine, procaine, and lidocaine were much closer to that of histamine than bupivacaine and ropivacaine. This was not only in line with the Ca2+ responses in activating H1R, but also consistent with the same amino acid residues shared with histamine in the H1R active site. In conclusion, this study provided new insight into the interactions between local anesthetics and H1R. The H1R-HEK293/CMC methods developed in this study could be used to evaluate the interaction characteristics of those compounds acting on H1R. (C) 2021 Elsevier B.V. All rights reserved.
机译:局部麻醉药在临床实践中有着广泛的应用。然而,据报道,局部麻醉剂引起的不良反应血管水肿与组胺H-1受体(H1R)有关。因此,需要一种有效且实用的方法来研究局麻药与H1R之间的相互作用特征。在这项工作中,基于H1R-HEK293/细胞膜色谱(CMC)的竞争结合分析和相对标准方法被开发用于分析局部麻醉剂与H1R的平衡离解常数(K-D)值。通过细胞内钙离子成像分析评估药物对H1R的活性。分子对接用于验证H1R蛋白激活区的相互作用模式。结果表明,局麻药能直接占据H1R上的组胺结合位点,不同CMC方法测得的K-D值呈显著正相关(p<0.01)。丁卡因、普鲁卡因和利多卡因的K-D值比布比卡因和罗哌卡因更接近组胺。这不仅与激活H1R的Ca2+反应一致,而且与H1R活性部位与组胺共享的相同氨基酸残基一致。总之,这项研究为局部麻醉剂和H1R之间的相互作用提供了新的见解。本研究中开发的H1R-HEK293/CMC方法可用于评估作用于H1R的化合物的相互作用特性。(c)2021爱思唯尔B.V.保留所有权利。

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