TRPC4/5 inhibitors: Phase I results and proof of concept studies.

Eur Arch Psychiatry Clin Neurosci

Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany.

Published: September 2024

AI Article Synopsis

  • TRPC ion channels are linked to emotion and mood regulation in the brain and are important in disorders like major depression and anxiety.
  • Research suggests that blocking TRPC4 and TRPC5 channels may help reduce fear and anxiety in mice without adversely affecting other behaviors.
  • Clinical trials with BI 1358894, a TRPC4/5 inhibitor, showed promise in reducing anxiety responses in humans, but more research is needed to confirm its effectiveness as a treatment for anxiety and mood disorders.

Article Abstract

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.

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Source
http://dx.doi.org/10.1007/s00406-024-01890-0DOI Listing

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