Chemosensory signaling through the vagus nerve is an important component of the gut-brain axis, relaying information about the presence of nutrients and irritants within the lumen of the gut. Vagal sensory neurons transmit these signals from the gut to the brainstem, activating neural circuits to modulate the rate of digestion, or trigger emesis or diarrhea. Although the physiology of this circuit has been studied for decades, only recently have the molecular details of the receptors, cells, and signaling mechanisms begun to be defined. Pioneering work has identified two specific populations of vagal sensory neurons that play distinct roles for signaling stretch in the stomach and nutrients in the duodenum. This demonstrates that vagal neurons can encode sensory information in a labeled-line fashion, ie one line for stretch, one line for nutrients. Apart from these two specific vagal sensory populations innervating the gut, other populations of neurons responsible for irritant sensing, or nutrient sensing outside of the duodenum/proximal intestine remain undefined. Basic information about the repertoire of vagal sensory neurons innervating the gut and the types of information they encode are lacking. The goal of this proposal is to define the chemosensory circuits for detecting nutrients and irritants in the gut by addressing the following questions: 1) How is gut nutrient and irritant information encoded by vagal sensory neurons? 2) Can activity dependent labeling techniques be used for circuit mapping and molecular characterization of functional subsets of vagal sensory neurons?

Public Health Relevance

The vagus nerve innervates the trachea, lungs, heart, liver, kidneys and gastrointestinal tract and serves as a multi-modal information conduit from the viscera to the brain (and back). Despite the important role of vagal sensory neurons in sensing and maintaining autonomic nervous system function, very little is known about their molecular receptors and signaling mechanisms. The focus of the project proposed here is to begin to fill in some basic gaps in our knowledge of the chemosensory neurons innervating the gut which will lay the foundation for future translational studies to tackle significant issues in human health including obesity, nausea and emesis, and inflammatory bowel disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Pilot Research Project (SC2)
Project #
5SC2GM130411-02
Application #
9843154
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Krasnova, Irina N
Project Start
2019-01-01
Project End
2021-12-31
Budget Start
2020-01-01
Budget End
2020-12-31
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
800189185
City
San Antonio
State
TX
Country
United States
Zip Code
78249