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Pathway

Fullness hormone (PYY)

The Gut Veto

1 blend on this site modulates it.

This is a third separate way that eating shuts fat release down, alongside insulin and the short-chain fatty acids that fiber fermentation produces. It is released particularly in response to protein and fiber. Nothing here is a criticism of eating well — it is simply why the timing of a fat-release product is not a detail.

In depth

A hormone released by the gut after eating that binds the same brake receptor as the stress peptide.

What drives it

Gut barrier increases it.

Distal-gut enteroendocrine L cells secrete peptide YY in response to luminal nutrients. PMID 26258126

What it drives

It increases The Stress Veto.

10.1371/journal.pone.0040038 — from a published diagram titled 'control DE LA LIPÓLISIS EN EL adipocito HUMANO' — a human-specific control map. Its legend enumerates the whole system: 'Receptores β- y α2A-Adrenérgicos (RA); Adenilato Ciclasa (AC); proteínas G heterotriméricas (Gs y Gi); Proteína Cinasa A (PKA); Lipasa Sensible a Hormona (LSH); Receptor de Insulina (IRS-1/2); Proteína Cinasa B (PKB); Cinasa (PI3-K); Fosfodiesterasa tipo 3B (PDE-3B); GUANILATO Ciclasa (GC); Receptor de Péptidos Natriuréticos (NPR-A); Proteína Cinasa G (PKG); Lipasa de Monoglicéridos (LMG); NEUROPÉPTIDO Y (NPY) Y PÉPTIDO YY (PYY); Proteínas que enlazan lípidos en adipocito (ALBP); Ácidos Grasos No Esterificados (AGNE)' (Revista de Educación Bioquímica, UNAM — 'Control de la lipólisis en el adipocito HUMANO' (ESPAÑOL)). A seventh veto ligand, named alongside the sixth in the same legend. Peptide YY shares the same receptor family as neuropeptide Y, and it is a gut hormone released after eating — particularly in response to protein and fiber. That is the third separate mechanism by which eating shuts this system down, alongside insulin and the short-chain fatty acids that fiber fermentation produces. The fasted rule keeps earning itself. doi 10.1371/journal.pone.0040038

It reduces Releases stored fat.

10.1016/S0022-2275(20)39879-5 — 10.1172/JCI114425 — from a published diagram titled 'control DE LA LIPÓLISIS EN EL adipocito HUMANO' — a human-specific control map. Its legend enumerates the whole system: 'Receptores β- y α2A-Adrenérgicos (RA); Adenilato Ciclasa (AC); proteínas G heterotriméricas (Gs y Gi); Proteína Cinasa A (PKA); Lipasa Sensible a Hormona (LSH); Receptor de Insulina (IRS-1/2); Proteína Cinasa B (PKB); Cinasa (PI3-K); Fosfodiesterasa tipo 3B (PDE-3B); GUANILATO Ciclasa (GC); Receptor de Péptidos Natriuréticos (NPR-A); Proteína Cinasa G (PKG); Lipasa de Monoglicéridos (LMG); NEUROPÉPTIDO Y (NPY) Y PÉPTIDO YY (PYY); Proteínas que enlazan lípidos en adipocito (ALBP); Ácidos Grasos No Esterificados (AGNE)' (Revista de Educación Bioquímica, UNAM — 'Control de la lipólisis en el adipocito HUMANO' (ESPAÑOL)). A seventh veto ligand, named alongside the sixth in the same legend. Peptide YY shares the same receptor family as neuropeptide Y, and it is a gut hormone released after eating — particularly in response to protein and fiber. That is the third separate mechanism by which eating shuts this system down, alongside insulin and the short-chain fatty acids that fiber fermentation produces. The fasted rule keeps earning itself. doi 10.1016/S0022-2275(20

Blends that modulate it

Each blend page names this pathway and carries the study behind its claim.

Lipolytic (Stored-Fat Mobilization) →

See it on the map

Open the causal map to follow this pathway upstream and downstream, arrow by arrow, each with its study.

All 567 pathways · All botanicals

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