Digestive System
Navigational overlay for the gastrointestinal tract, liver, pancreas, and the gut microbiome. The best-developed aging biology in this system is currently the gut microbiome — its compositional drift, barrier failure (“leaky gut”), and contribution to inflammaging are an active research front and a dedicated hallmark (dysbiosis). Solid-organ pages (liver, intestine, pancreas) are largely planned.
Processes & barrier biology
- gut-barrier — intestinal barrier integrity; “leaky gut” and systemic inflammaging
- gut-microbiome-aging-shifts — age-related compositional change
Microbiome (atomic taxa)
- firmicutes-bacteroidetes-ratio — the most-cited aging microbiome metric
- akkermansia-muciniphila · bifidobacterium · lactobacillus — taxa with aging-relevant shifts
- ewingella-americana — lower-vertebrate-derived therapeutic candidate
Aging phenotypes
- type-2-diabetes — metabolic disease with strong gut-microbiome and pancreatic-islet components (shared with endocrine-system)
Related interventions
- Dietary: caloric-restriction, ketogenic-diet, phosphate-additive-reduction; prebiotics/postbiotics/FMT
Auto-aggregated tissue members
LIST FROM "tissues"
WHERE parent-system = "digestive-system"
SORT file.nameMissing / planned pages
- liver and pancreas — now seeded as stubs (need full content); liver has an ingested primate snRNA aging study (yang-2023-primate-liver-aging-snrna-srebp2)
[[intestine]],[[stomach]],[[colon]],[[esophagus]],[[gallbladder]]— solid-organ/segment pages not yet seeded stub[[enterocytes]],[[intestinal-stem-cells]],[[hepatocytes]]— cell types not yet seeded stub
See also
- by-organ-system — index of all body-system MOCs
- dysbiosis — the gut-microbiome hallmark
- endocrine-system — pancreatic islets / glucose homeostasis overlap