mTOR Pathway Suppression refers to the pharmacological or nutritional inhibition of the mammalian Target of Rapamycin (mTOR) signaling cascade, a central regulator of cell growth, proliferation, and protein synthesis. Transient suppression of this pathway is a key strategy in longevity and metabolic health, as it is a potent trigger for catabolic and cellular recycling processes, notably autophagy. This modulation is critical for shifting the cellular balance from growth toward repair.
Origin
The mTOR protein was initially identified as the target of the immunosuppressant drug Rapamycin, hence its name. The realization that this pathway acts as a master nutrient sensor linking growth factors, amino acids, and cellular energy status to cellular aging established its profound importance in longevity science. Suppression is now a central focus of metabolic research.
Mechanism
mTOR acts as a sensor of nutrient abundance; when activated by insulin, growth factors, and high amino acid levels, it promotes anabolic processes and inhibits autophagy. Suppression, often achieved through nutrient deprivation like fasting or with compounds like Rapamycin, leads to the dephosphorylation of key regulatory proteins. This molecular event effectively turns off the growth signal and activates the AMPK and sirtuin pathways, initiating the degradation of damaged cellular components and promoting cellular stress resistance and renewal.
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