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5-HT1B/1D受体拮抗剂和激动剂的最新进展及其潜在治疗应用。

Recent advances in 5-HT1B/1D receptor antagonists and agonists and their potential therapeutic applications.

作者信息

Slassi Abdelmalik

机构信息

Medicinal Chemistry Department, NPS Pharmaceuticals, 6850 Goreway Drive, Mississauga, Ontario, L4V 1V7, Canada.

出版信息

Curr Top Med Chem. 2002 Jun;2(6):559-74. doi: 10.2174/1568026023393903.

DOI:10.2174/1568026023393903
PMID:12052194
Abstract

The human 5-HT(1B) and 5-HT(1D) receptors are especially similar in sequence despite being encoded by two distinct genes. Although, human 5-HT(1B) and 5-HT(1D) receptors have been pharmacologically differentiated using nonselective 5-HT(1B/D) receptor antagonists such as ketanserin (1), ritanserin (2) and methiothepin (3), the precise function of these receptors remains undefined, and progress toward this has been hampered by the lack of selective ligands. The interest of the major pharmaceutical companies in 5-HT(1B/1D) antagonists increased by the discovery of potent and selective tools, combined with the fact that the blockade of terminal 5-HT(1B) receptors by selective antagonists has been proposed as a new approach for more efficient and/or fast-acting antidepressant drugs, since the acute blockade of these 5-HT autoreceptors will, in theory, immediately mimic their desensitization. Furthermore, it has been also suggested that supersensitive 5-HT(1B/1D) receptors may be involved in the pathophysiology of obsessive compulsive disorders (OCD). In the 5-HT(1B/1D) agonist field, since the discovery of sumatriptan (26) (a 5-HT(1B/1D) receptor agonist) as an effective treatment for migraine headache, intensive research in this area has led to several second-generation compounds, a few of which have either entered the market place or are in late clinical trials. Beside the antimigraine activity of the 5-HT(1B/1D) agonists in clinical evaluation or already on the market, other potential therapeutic evaluations (such as gastric motor effect, bipolar disorder, autism, anti-aggressive effects) with these drugs are being investigated. This article highlights and reviews the research advances published in the 5-HT(1B/1D) antagonist and agonist literature. The article is supplemented with selected references on the design, synthesis and development of novel 5-HT(1B/1D) agents, and on studies to understand their mechanism and pathophysiology. Emphasis is given to recent advances in the potential therapeutic applications of 5-HT(1B/1D) serotonergic agents. By no means has any attempt been made to exhaustively review the literature but rather, primary references along with citations to recent literature reviews have been included in each section.

摘要

尽管人类5-HT(1B)和5-HT(1D)受体由两个不同的基因编码,但它们在序列上特别相似。虽然,人类5-HT(1B)和5-HT(1D)受体已通过使用非选择性5-HT(1B/D)受体拮抗剂(如酮色林(1)、利坦色林(2)和甲硫噻平(3))进行了药理学区分,但这些受体的确切功能仍未明确,且由于缺乏选择性配体,在此方面的进展受到了阻碍。主要制药公司对5-HT(1B/1D)拮抗剂的兴趣因发现了强效且选择性的工具而增加,同时,由于理论上选择性拮抗剂对终末5-HT(1B)受体的阻断被提议作为一种开发更高效和/或速效抗抑郁药物的新方法,因为对这些5-HT自身受体的急性阻断将立即模拟它们的脱敏状态。此外,也有人提出超敏的5-HT(1B/1D)受体可能参与强迫症(OCD)的病理生理学过程。在5-HT(1B/1D)激动剂领域,自从发现舒马曲坦(26)(一种5-HT(1B/1D)受体激动剂)可有效治疗偏头痛以来,该领域的深入研究已产生了几种第二代化合物,其中一些已进入市场或正处于后期临床试验阶段。除了5-HT(1B/1D)激动剂在临床评估或已上市产品中的抗偏头痛活性外,这些药物的其他潜在治疗评估(如胃动力效应、双相情感障碍、自闭症、抗攻击效应)也正在研究中。本文重点介绍并综述了5-HT(1B/1D)拮抗剂和激动剂文献中发表的研究进展。文章还补充了关于新型5-HT(1B/1D)药物的设计、合成和开发以及旨在了解其作用机制和病理生理学的研究的精选参考文献。重点是5-HT(1B/1D)血清素能药物在潜在治疗应用方面的最新进展。本文绝没有试图详尽地综述文献,而是在每个章节中都纳入了主要参考文献以及对近期文献综述的引用。

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