bioRxiv · 10.64898/2026.01.15.699765
THIK-1 channel mediates microglial glucose sensing and modulates AgRP neurons
Abstract
Microglia play essential roles in maintaining energy homeostasis, and their dysfunction contributes to metabolic disease. Although high-fat diet (HFD) exposure induces microglial activation, the underlying mechanisms remain poorly defined. Here, we identified a previously unrecognized role for THIK-1 channel in mediating glucose sensing of microglia in arcuate nucleus of the hypothalamus (ARH), during HFD-induced obesity. Pharmacological inhibition of THIK-1 channel with tetrapentylammonium (TPA) suppresses feeding and attenuates body-weight gain in diet induced obese mice. Mechanistically, inhibition of agouti-related peptide (AgRP) neurons is indispensable for TPA-induced hypophagia. Moreover, THIK-1 inhibition promotes microglial phagocytosis of perineuronal nets (PNNs), leading to reduced AgRP neuronal activity and feeding suppression. Together, these findings establish THIK-1 as a critical glucose sensor in hypothalamic microglia and uncover a microglia-dependent pathway through which overnutrition modulates AgRP neuronal activity via PNN remodeling to regulate energy balance, highlighting THIK-1 as a potential therapeutic target for treatment of diet-induced obesity.
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Liu, Q., Bean, J. C., Jian, J., Zhou, T., Yang, Y., Sun, M., Li, Y., Conde, K. M., Wang, M., Deng, Y., Qiu, J., Wang, F., Liu, X., Liu, Y., Cheng, J., Wu, X., Xue, L., Chen, C., Meng, C., Zhu, Y., Tu, L., Liu, H., Xu, Y.. 2026-01-16. THIK-1 channel mediates microglial glucose sensing and modulates AgRP neurons. https://doi.org/10.64898/2026.01.15.699765
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