Worldwide Discovery Research, Cephalon, Inc., West Chester, PA 19380, USA.
Curr Top Med Chem. 2010;10(2):153-69. doi: 10.2174/156802610790411027.
The H(3) histamine receptor is expressed in many brain regions, including those involved in sleep/wake regulation and cognitive functions. Inhibition of the H(3) receptor leads to increased release of multiple neurotransmitters in these regions, making this receptor an ideal target for the potential enhancement of arousal and/or cognitive processes. The high interest level by several pharmaceutical companies in H(3) receptors as potential drug targets has produced rapid advancement in novel compound series with different properties, providing a variety of preclinical tools as well as advancing several candidates into clinical trials. Multiple chemotypes have demonstrated efficacy in preclinical models covering a range of cognitive deficits, suggesting the potential value of H(3) antagonists as cognition enhancers in a variety of disease states. These studies have revealed the actions of this class of compounds at the cellular, neuronal systems and behavioral levels. Recently, compounds with improved selectivity, pharmacokinetics and preclinical safety profiles have advanced into clinical trials for a number of potential indications. The results of these clinical trials are eagerly awaited and will increase our understanding of the properties of H(3) receptor antagonists that will provide therapeutic value.
H3 组胺受体在许多脑区表达,包括参与睡眠/觉醒调节和认知功能的脑区。H3 受体的抑制导致这些脑区中多种神经递质的释放增加,使该受体成为潜在增强觉醒和/或认知过程的理想靶点。多家制药公司对 H3 受体作为潜在药物靶点的高度关注,推动了具有不同特性的新型化合物系列的快速发展,提供了多种临床前工具,并使几种候选药物进入临床试验。多种化学型已在涵盖一系列认知缺陷的临床前模型中证明了疗效,这表明 H3 拮抗剂作为多种疾病状态下的认知增强剂具有潜在价值。这些研究揭示了该类化合物在细胞、神经元系统和行为水平上的作用。最近,具有改善的选择性、药代动力学和临床前安全性特征的化合物已在多种潜在适应症的临床试验中取得进展。这些临床试验的结果备受期待,将增加我们对 H3 受体拮抗剂特性的理解,从而提供治疗价值。