Serotonin
215 sourcesRay Peat's view of serotonin is one of his most radical departures from mainstream thinking. While popular culture and psychiatry treat serotonin as a 'happiness molecule' whose deficiency causes depression, Peat argued that serotonin is fundamentally a stress and inflammation mediator. He documented extensive evidence that serotonin promotes intestinal inflammation, blood clotting, bronchoconstriction, fibrosis, and cancer — and that SSRI antidepressants work not by correcting a deficiency but by desensitizing serotonin receptors over time.
Peat traced the serotonin myth to pharmaceutical marketing and noted that tryptophan (serotonin's precursor) increases under stress as muscle protein breaks down. He recommended reducing serotonin through dietary means (avoiding excess tryptophan from muscle meats, preferring gelatin-rich foods), using anti-serotonin agents (cyproheptadine, ondansetron), and supporting opposing systems (thyroid, progesterone, dopamine).
Key Positions
- Serotonin is primarily a stress and inflammation mediator, not a 'happiness molecule'
- 90% of the body's serotonin is in the gut, where it promotes inflammation and peristalsis
- SSRIs work by eventually desensitizing serotonin receptors, not by correcting a deficiency
- Tryptophan (serotonin precursor) is released from stressed muscle tissue
- Gelatin/collagen protein is low in tryptophan and can help reduce serotonin
- Serotonin promotes cancer cell growth, fibrosis, and blood vessel constriction
- Anti-serotonin agents (cyproheptadine, ondansetron) have anti-inflammatory and anti-cancer effects
Sources
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