Grimm Simone, Just Stefan, Fuertig Rene, Dwyer Jennifer B, Sharma Vikas M, Wunder Andreas
Medical School Berlin, Rüdesheimer Str., 5014197, Berlin, Germany.
Department of Psychiatry, Campus Benjamin Franklin Charité, Berlin, Germany.
Eur Arch Psychiatry Clin Neurosci. 2024 Sep 29. doi: 10.1007/s00406-024-01890-0.
Transient receptor potential canonical (TRPC) ion channels are expressed in areas of the brain responsible for processing emotion and mood and have been implicated in the pathophysiology of internalizing disorders such as major depressive disorder and anxiety disorders. This review outlines the rationale for targeting TRPC ion channels for drug development, with specific focus on TRPC4 and TRPC5. We provide preclinical evidence that the lack of TRPC4 and TRPC5 channels or its pharmacological inhibition attenuate fear and anxiety without impairing other behaviors in mice. We also report on clinical studies of BI 1358894, a small molecule inhibitor of TRPC4/5 ion channels, demonstrating reduced psychological and physiological responses to induced anxiety/panic-like symptoms in healthy volunteers. Furthermore, we highlight an imaging study that investigated the acute effects of BI 1358894 and showed reduced activation in several brain regions involved in emotional processing. We conclude that these findings demonstrate a critical role for TRPC4 and TRPC5 in emotional processing, even though it remains an open question if the biological signatures of TRPC4/5 inhibition reported here translate into clinical efficacy and indicate that a TRPC4/5 inhibitor might provide a more effective treatment of internalizing disorders.
瞬时受体电位香草酸亚型(TRPC)离子通道在大脑中负责处理情绪和心境的区域表达,并与诸如重度抑郁症和焦虑症等内化性障碍的病理生理学有关。本综述概述了将TRPC离子通道作为药物开发靶点的基本原理,特别关注TRPC4和TRPC5。我们提供临床前证据表明,缺乏TRPC4和TRPC5通道或其药理抑制作用可减轻小鼠的恐惧和焦虑,而不损害其他行为。我们还报告了TRPC4/5离子通道小分子抑制剂BI 1358894的临床研究,该研究表明健康志愿者对诱发的焦虑/惊恐样症状的心理和生理反应有所降低。此外,我们重点介绍了一项成像研究,该研究调查了BI 1358894的急性效应,并显示在几个参与情绪处理的脑区激活减少。我们得出结论,这些发现证明了TRPC4和TRPC5在情绪处理中起关键作用,尽管此处报道的TRPC4/5抑制的生物学特征是否转化为临床疗效仍是一个悬而未决的问题,并表明TRPC4/5抑制剂可能为内化性障碍提供更有效的治疗方法。