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Showing papers by "Thomas Baukrowitz published in 2023"


Journal ArticleDOI
TL;DR: In this article , the TWIK-related potassium channel 1 (TREK1) activators were identified and validated using patch-clamp measurements of Xenopus laevis oocytes expressing TREK1.
Abstract: Abstract Modulation of two-pore domain potassium (K2P) channels has emerged as a novel field of therapeutic strategies as they may regulate immune cell activation and metabolism, inflammatory signals, or barrier integrity. One of these ion channels is the TWIK-related potassium channel 1 (TREK1). In the current study, we report the identification and validation of new TREK1 activators. Firstly, we used a modified potassium ion channel assay to perform high-throughput-screening of new TREK1 activators. Dose-response studies helped to identify compounds with a high separation between effectiveness and toxicity. Inside-out patch-clamp measurements of Xenopus laevis oocytes expressing TREK1 were used for further validation of these activators regarding specificity and activity. These approaches yielded three substances, E1, B3 and A2 that robustly activate TREK1. Functionally, we demonstrated that these compounds reduce levels of adhesion molecules on primary human brain and muscle endothelial cells without affecting cell viability. Finally, we studied compound A2 via voltage-clamp recordings as this activator displayed the strongest effect on adhesion molecules. Interestingly, A2 lacked TREK1 activation in the tested neuronal cell type. Taken together, this study provides data on novel TREK1 activators that might be employed to pharmacologically modulate TREK1 activity.

1 citations


Journal ArticleDOI
TL;DR: In this paper , a lower gate in the cardiac two-pore domain K+ channel K2P17.1 (TALK-2, TASK-4) was shown to produce state-dependent pore access of intracellular applied blockers and cysteine modifying probes similar to the helix-bundle crossing gate in voltage-gated Kv channels.