Senescence / Autophagy
In one line: Ageing is partly a garbage problem — old "zombie" cells that won't die, and cellular junk that needs recycling.
Picture this: Two housekeeping systems keep cells young. Autophagy is the cell's recycling program — it breaks down damaged parts and reuses them (fasting and exercise switch it on). Senescence is the opposite problem: some damaged cells refuse to die and instead sit around leaking inflammation — "zombie cells." Senolytics are compounds that clear those zombies out.
Step by step:
- Over time, cells accumulate damaged parts (junk) and some become senescent (zombies).
- Autophagy recycles the junk — triggered by low mTOR, high AMPK, fasting, and exercise.
- Zombie cells, meanwhile, secrete inflammatory signals that age nearby tissue.
- Senolytic compounds selectively kill those zombie cells, reducing the inflammation.
Why it matters for you: This is the frontier of longevity. Fisetin (taken as a monthly 2-day pulse) clears zombie cells; spermidine and rapamycin boost recycling. Fasting and exercise do both for free.
Turn it up: fisetin and quercetin (clear zombies), spermidine and rapamycin (boost recycling), fasting, exercise. Don't be fooled: senolytics are pulsed (a couple of days), not taken daily — and the human evidence is still early, however compelling the mechanism.
The whole map in one paragraph
Building muscle lives on mTOR + the androgen receptor + growth-factor signalling. Losing fat lives on the cAMP doorbell (stimulants), GLP-1, and AMPK. Focus and mood live on dopamine/serotonin, acetylcholine, and the GABA brake. Longevity lives on AMPK (up), mTOR (down), NAD⁺, cleanup crews, and healthy mitochondria. Hormones run through the testosterone loop, the stress axis, and nuclear receptors. Recovery and blood flow run through nitric oxide, growth-factor healing, and turning inflammation down. Sixteen switches — learn them, and every compound on this site becomes something you can reason about yourself.