Abstract
Ingestion of a meal triggers a range of physiological responses both within and outside the gut, and results in the remote modulation of appetite and glucose homeostasis. Luminal contents are sensed by specialised chemosensitive cells scattered throughout the intestinal epithelium. These enteroendocrine and tuft cells make direct contact with the gut lumen and release a range of chemical mediators, which can either act in a paracrine fashion interacting with neighbouring cells and nerve endings or as classical circulating hormones. At the molecular level, the chemosensory machinery involves multiple and complex signalling pathways including activation of G-protein-coupled receptors and solute carrier transporters. This chapter will discuss our current knowledge of the molecular mechanisms underlying intestinal chemosensation with a particular focus on the relatively well-characterised nutrient-triggered secretion from the enteroendocrine system.
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Abbreviations
- 2-APB:
-
2-Aminoethoxydiphenyl borate
- 5-HT:
-
Serotonin
- CaMK:
-
Ca2+/calmodulin-dependent protein kinases
- cAMP:
-
Cyclic adenosine monophosphate
- CCK:
-
Cholecystokinin
- DGAT1:
-
Diacylglycerol acyltransferase 1
- EC:
-
Enterochromaffin cell
- FFA:
-
Free fatty acids
- GIP:
-
Glucose-dependent insulinotropic polypeptide
- GLP:
-
Glucagon-like peptide
- GPCR:
-
G-protein-coupled receptor
- LCFA:
-
Long-chain fatty acids
- MTP:
-
Microsomal triglyceride transfer protein
- NOPE:
-
N-oleoyl-phosphatidylethanolamine
- OEA:
-
Oleoylethanolamide
- PKA:
-
Protein kinase A
- PKC:
-
Protein kinase C
- PLC:
-
Phospholipase C
- PYY:
-
PeptideYY
- SCFA:
-
Short-chain fatty acids
- SLC:
-
Solute carrier transporters
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FMG, GT and FR are supported by grants from the Wellcome Trust ((#WT088357, #WT084210).
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Tolhurst, G., Reimann, F., Gribble, F.M. (2012). Intestinal Sensing of Nutrients. In: Joost, HG. (eds) Appetite Control. Handbook of Experimental Pharmacology, vol 209. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-24716-3_14
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