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评估抗组胺药反向激动活性的希拉细胞的有用性。

Usefulness of HeLa cells to evaluate inverse agonistic activity of antihistamines.

机构信息

Department of Molecular Pharmacology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima 770-8505, Japan.

出版信息

Int Immunopharmacol. 2013 Mar;15(3):539-43. doi: 10.1016/j.intimp.2013.02.009. Epub 2013 Feb 20.

Abstract

Antihistamines are thought to antagonize histamine and prevent it from binding to the histamine H1 receptor (H1R). However, recent studies indicate that antihistamines are classified into two groups, i.e., inverse agonists and neutral antagonists on the basis of their ability to down-regulate the constitutive activity of H1R. As H1R is an allergy-sensitive gene whose expression influences the severity of allergic symptoms, inverse agonists should more potently alleviate allergic symptoms than neutral antagonists by inhibiting H1R constitutive activity. Therefore, it is important to assess inverse agonistic activity of antihistamines. Here we report a novel assay method using HeLa cells expressing H1R endogenously for evaluation of inverse agonistic activity of antihistamines. Pretreatment with inverse agonists down-regulated H1R gene expression below to its basal level. On the other hand, basal H1R mRNA expression was unchanged by neutral antagonist pretreatment. Both inverse agonists and neutral antagonists suppressed histamine-induced H1R mRNA elevation. Classification of antihistamines on the basis of their suppressive activity of basal H1R gene expression was consistent with that of inositol phosphate accumulation in H1R-overexpressed cells. Our data suggest that the assay method using HeLa cells is more convenient and useful than the existing methods and may contribute to develop new antihistamines with inverse agonistic activity.

摘要

抗组胺药被认为可以拮抗组胺并防止其与组胺 H1 受体(H1R)结合。然而,最近的研究表明,根据其下调 H1R 组成型活性的能力,抗组胺药可分为两类,即反向激动剂和中性拮抗剂。由于 H1R 是一种过敏敏感基因,其表达影响过敏症状的严重程度,因此通过抑制 H1R 组成型活性,反向激动剂应比中性拮抗剂更有效地缓解过敏症状。因此,评估抗组胺药的反向激动活性非常重要。在这里,我们报告了一种使用内源性表达 H1R 的 HeLa 细胞的新型测定方法,用于评估抗组胺药的反向激动活性。预处理与下调反向激动剂 H1R 基因表达低于其基础水平。另一方面,中性拮抗剂预处理对基础 H1R mRNA 表达没有影响。反向激动剂和中性拮抗剂均抑制组胺诱导的 H1R mRNA 升高。根据对基础 H1R 基因表达的抑制活性对抗组胺药进行分类,与在 H1R 过表达细胞中积累的肌醇磷酸一致。我们的数据表明,使用 HeLa 细胞的测定方法比现有方法更方便、更有用,可能有助于开发具有反向激动活性的新型抗组胺药。

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