The deliberate, cyclical modulation of the Mammalian Target of Rapamycin (mTOR) signaling pathway, alternating between periods of activation (anabolic state) and suppression (catabolic/autophagic state), typically achieved through strategic nutrient timing and intake. This cycling is a biohacking and clinical strategy aimed at optimizing muscle protein synthesis while periodically engaging cellular cleansing mechanisms to promote cellular longevity and metabolic health.
Origin
The concept stems from the fundamental understanding of the mTOR pathway as the central regulator of cell growth, proliferation, and survival, which is highly sensitive to amino acid and energy availability. “Cycling” represents the translational application of longevity research, suggesting that periodic inhibition is beneficial.
Mechanism
High intake of amino acids, particularly leucine, and the presence of insulin strongly activate the mTOR pathway, driving protein synthesis and cellular growth. Conversely, periods of fasting or calorie restriction lead to the deactivation of mTOR, which then permits the upregulation of autophagy, a critical cellular process for clearing damaged organelles and proteins. Strategic cycling seeks to leverage both the anabolic benefits of mTOR activation and the longevity benefits of its temporary suppression.
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