Cholecystokinin
low riskAlso: CCK · CCK-8 · Satiety hormone
Reference entry for cholecystokinin (CCK), the primary GI satiety hormone released from duodenal I-cells in response to fat and protein. Signals fullness via vagal afferents and hypothalamic CCK receptors. CCK-1 receptor agonism is a drug target for obesity.
Reported Benefits
Satiety signaling
Well-characterized GI satiety hormone. CCK-1 receptor agonism is active drug target for obesity pharmacology.
Mechanism of Action
Released from duodenal I-cells post-meal; acts on CCK-1 (CCK-A) receptors on vagal afferents; stimulates pancreatic enzyme and bile secretion; inhibits gastric emptying; signals satiety to hypothalamus.
Relevance to Obesity Pharmacology
CCK-1 receptor agonists are an active target class for obesity drug development. Understanding native CCK physiology provides context for interpreting early-stage compounds targeting this pathway.
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Regulatory Status
Research OnlySafety Profile
Side Effects
- •Not applicable
Contraindications
- •N/A
Primary Uses
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