ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude

ISX-9 增强 CaMKIIδ 介导的 BMAL1 激活以增强昼夜节律

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作者:Huilin Li #, Jiali Ou #, Yaqun Li, Niannian Xu, Qing Li, Ping Wu, Chao Peng, Yun-Chi Tang, Hung-Chun Chang

Abstract

Circadian dysregulation associates with numerous diseases including metabolic dysfunction, sleep disorder, depression and aging. Given that declined circadian amplitude is a trait commonly found with compromised health, interventions that design in precluding circadian amplitude from dampening will aid to mitigate complex, circadian-related diseases. Here we identify a neurogenic small molecule ISX-9 that is able to support persistent and higher amplitude of circadian oscillations. ISX-9 improves diurnal metabolic rhythms in middle-aged mice. Moreover, the ISX-9-treated mice show better sleep homeostasis with increased delta power during the day time and higher locomotive activity in the dark period. ISX-9 augments CaMKIIδ expression and increases BMAL1 activity via eliciting CaMKIIδ-mediated phosphorylation on BMAL1 residues S513/S515/S516, accordingly composes a positive feedback effect on enhancing circadian amplitude. CaMKIIδ-targeting, and the use of ISX-9 may serve as decent choices for treating circadian-related disorders.

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