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组胺 H₄ 受体:炎症治疗的新靶点。

Histamine H₄ receptor: a novel target for inflammation therapy.

机构信息

Pharmaceutical Chemistry Research Laboratory, Department of Pharmaceutics, Institute of Technology, Banaras Hindu University, Varanasi- 221005, India.

出版信息

Mini Rev Med Chem. 2011 Feb;11(2):143-58. doi: 10.2174/138955711794519519.

Abstract

Histamine, a low molecular weight amine has been extensively studied for its various pharmacological profiles. Until recently histamine was thought to act on three receptors - H₁, H₂ and H₃. Merely a decade back, sequencing of human genome has revealed a new histamine receptor - H₄ receptor. This 390 amino acid sequenced receptor has around 38% homology with histamine H₃ receptor besides; the pharmacological profile of the protein is quite different from other histamine receptors. H₄ receptor is mainly expressed in mast cells and leukocytes and involves various physiological functions related to inflammation and allergy. Potent selective H₄ receptor agonists and antagonists have been synthesized and in vivo studies have indicated their action on H₄ receptor. In this review, structure, expression, homology sequence of H₄ receptor among the different species has been documented. Further, structure activity relationship (SAR) of H₄ ligands on the basis of their nucleus has been discussed in depth. In addition, anti-inflammatory effects of H₄ receptor antagonists, with special emphasis to JNJ7777120, a selective H₄ receptor antagonist have been focused exhaustively.

摘要

组胺是一种低分子量的胺,因其各种药理学特性而被广泛研究。直到最近,人们认为组胺作用于三种受体——H₁、H₂和 H₃。仅仅十年前,人类基因组测序揭示了一种新的组胺受体——H₄ 受体。这种 390 个氨基酸序列的受体与组胺 H₃ 受体有大约 38%的同源性;此外,该蛋白的药理学特征与其他组胺受体有很大的不同。H₄ 受体主要表达在肥大细胞和白细胞中,涉及与炎症和过敏相关的各种生理功能。已经合成了强效选择性 H₄ 受体激动剂和拮抗剂,并进行了体内研究,表明它们对 H₄ 受体的作用。在这篇综述中,记录了不同物种中 H₄ 受体的结构、表达和同源序列。此外,还深入讨论了基于核的 H₄ 配体的结构活性关系(SAR)。此外,还专门关注了 H₄ 受体拮抗剂的抗炎作用,特别强调了选择性 H₄ 受体拮抗剂 JNJ7777120。

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