Satiety Signaling Pathways encompass the complex, integrated neuroendocrine circuits that originate primarily in the gastrointestinal tract and adipose tissue, converging on the hypothalamus to communicate the state of energy sufficiency and suppress the drive to eat. These pathways involve the coordinated release and action of numerous gut peptides and adipokines, such as GLP-1, PYY, CCK, and leptin, which collectively terminate a meal and regulate inter-meal interval. Functional integrity of these pathways is essential for natural weight management.
Origin
The detailed understanding of these pathways is a relatively modern development in endocrinology and neurobiology, following the discovery of key regulatory hormones and their central nervous system targets. The concept emphasizes a multi-hormonal, network-based control system rather than a single hunger switch.
Mechanism
Upon food ingestion, enteroendocrine cells in the gut release peptides like GLP-1 and PYY, which travel via the bloodstream and vagus nerve to the brainstem and arcuate nucleus of the hypothalamus. Simultaneously, leptin from fat cells signals long-term energy stores. These signals activate anorexigenic neurons and inhibit orexigenic neurons, creating the integrated sensation of fullness that governs subsequent food-seeking behavior.
We use cookies to personalize content and marketing, and to analyze our traffic. This helps us maintain the quality of our free resources. manage your preferences below.
Detailed Cookie Preferences
This helps support our free resources through personalized marketing efforts and promotions.
Analytics cookies help us understand how visitors interact with our website, improving user experience and website performance.
Personalization cookies enable us to customize the content and features of our site based on your interactions, offering a more tailored experience.