Targeting neuronal homeostasis to prevent seizures

Mulroe, F.; Lin, W.-H.; Mackenzie-Gray-Scott, C.; Aourz, N.; Fan, Y. N.; Coutts, G.; Parrish, R. R.; Smolders, I.; Trevelyan, A.; Wykes, R.; Allan, S. M.; Freeman, S.; Baines, R. A.

doi:10.1101/2022.03.07.483229

bioRxiv · 10.1101/2022.03.07.483229

Targeting neuronal homeostasis to prevent seizures

Mulroe, F.·Lin, W.-H.·Mackenzie-Gray-Scott, C.·Aourz, N.·Fan, Y. N.·Coutts, G.·Parrish, R. R.·Smolders, I.·Trevelyan, A.·Wykes, R.·Allan, S. M.·Freeman, S.·Baines, R. A.

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Abstract

Manipulating neuronal homeostasis, which enables neurons to regulate their intrinsic excitability, offers an attractive opportunity to prevent seizures. However, no anticonvulsant compounds have yet been reported that directly manipulate neuronal homeostasis. Here, we describe a novel class of anticonvulsant compounds, based on 4-tert-butyl-benzaldehyde (4-TBB), with a mode-of-action that includes increased expression of the homeostatic regulator Pumilio (Pum). In Drosophila and mouse we use a pentylenetetrazole (PTZ) induced seizure model, and an electrically induced seizure model for refractory seizures to evaluate anticonvulsant efficacy. The pyrazole analogue (RAB216) demonstrates best efficacy, protecting 50% of mice from PTZ-induced seizure. Knock-down of Pum, in Drosophila, blocks anticonvulsive effects, whilst analysis of validated Pum targets show significant reductions following exposure of mouse brain to 4-TBB. This study provides proof-of-principle that anticonvulsant effects can be achieved through regulation of neuronal homeostasis and identifies a chemical lead compound for future development.

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Mulroe, F., Lin, W.-H., Mackenzie-Gray-Scott, C., Aourz, N., Fan, Y. N., Coutts, G., Parrish, R. R., Smolders, I., Trevelyan, A., Wykes, R., Allan, S. M., Freeman, S., Baines, R. A.. 2022-03-07. Targeting neuronal homeostasis to prevent seizures. https://doi.org/10.1101/2022.03.07.483229

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