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bioRxiv · 10.1101/2023.08.24.554526

Cellular and Molecular Basis of Leptin Resistance

Tan, B.·Hedbacker, K.·Kelly, L.·Zhang, Z.·Luo, J.-D.·Rabinowitz, J. D.·Friedman, J. M.
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Abstract

Obese humans and diet induced obese mice (DIO) have high leptin levels and fail to respond to the exogenous hormone suggesting that obesity is caused by leptin resistance, the pathogenesis of which is unknown. We found that leptin treatment reduced plasma levels of mTOR ligands leading us to hypothesize that mTOR activation might inhibit leptin signaling. Rapamycin, an mTOR inhibitor, reduced fat mass and increased leptin sensitivity in DIO mice but not in mice with defects in leptin signaling. Rapamycin restored leptins actions on POMC neurons but failed to reduce the weight of mice with defects in melanocortin signaling. mTOR activation in POMC neurons caused leptin resistance while POMC specific mutations in mTOR activators decreased the weight gain of DIO mice. Thus increased mTOR activity in POMC neurons is necessary and sufficient for the development of leptin resistance in DIO mice establishing a key pathogenic mechanism leading to obesity.

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Tan, B., Hedbacker, K., Kelly, L., Zhang, Z., Luo, J.-D., Rabinowitz, J. D., Friedman, J. M.. 2023-08-26. Cellular and Molecular Basis of Leptin Resistance. https://doi.org/10.1101/2023.08.24.554526

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