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Am J Physiol Gastrointest Liver Physiol 292: G457-G461, 2007. First published November 9, 2006; doi:10.1152/ajpgi.00411.2006
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THEMES

Taste Receptors in the Gastrointestinal Tract. IV. Functional implications of bitter taste receptors in gastrointestinal chemosensing

Catia Sternini

Center for Ulcer Research and Education Digestive Diseases Research Center, Veterans Administration Greater Los Angeles Healthcare System, Digestive Diseases Division, Departments of Medicine and Neurobiology, David Geffen School of Medicine, University of California, Los Angeles, California

Submitted 2 September 2006 ; accepted in final form 31 October 2006

Changes in the luminal contents of the gastrointestinal tract modulate gastrointestinal functions, including absorption of nutrients, food intake, and protection against harmful substances. The current notion is that mucosal enteroendocrine cells act as primary chemoreceptors by releasing signaling molecules in response to changes in the luminal environment, which in turn activate nerve terminals. The recent discovery that taste receptors and G protein subunits {alpha}-gustducin and {alpha}-transducin, involved in gustatory signal transduction, are expressed in the gastrointestinal mucosa supports the concept of a chemosensory machinery in the gastrointestinal tract. An understanding of luminal sensing processes responsible for the generation of the appropriate functional response to specific nutrients and nonnutrients is of clinical importance since aberrant or unsteady responses to changes in luminal contents might result in disease states ranging from intoxication to feeding disorders and inflammation. The purpose of this theme article is to discuss the functional implications of bitter taste signaling molecules in the gastrointestinal tract deduced by their localization in selected populations of epithelial cells and their relationship with neural pathways responsible for the generation of specific responses to luminal contents.

{alpha}-gustducin; {alpha}-transducin; enteroendocrine cells; intrinsic afferent neurons; visceral afferent neurons; chemoreception



Address for reprint requests and other correspondence: C. Sternini, CURE Digestive Diseases Research Center, Bldg. 115, Rm. 224, VAGLAHS, 11301 Wilshire Blvd., Los Angeles, CA 90073 (e-mail: csternin{at}ucla.edu)




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