TY - JOUR
T1 - Regulation of the brain-gut axis by group III metabotropic glutamate receptors
AU - Julio-Pieper, Marcela
AU - O'Connor, Richard M.
AU - Dinan, Timothy G.
AU - Cryan, John F.
N1 - Funding Information:
The authors would like to thank Dr. Ken Nally, Dr. Monica Ambrose and Mr. Jerzy Woznicki for kindly providing human proximal colon RNA as well as cDNA for preliminary studies. The authors would also like to thank Dr. Sue Grenham for her expert technical assistance and helpful comments. MJ-P is supported by Conicyt (grant for Recruitment and Integration of Advanced Human Capital) and JFC, RMO and TGD are supported by Science Foundation Ireland (grant 02/CE/B124 and 07/CE/B1368 ) and European Community’s Seventh Framework Programme (grant FP7/2007–2013 , grant Agreement 201714 ). The funding sources had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
PY - 2013/1/5
Y1 - 2013/1/5
N2 - l-glutamate is produced by a great variety of peripheral tissues in both health and disease. Like other components of the glutamatergic system, metabotropic glutamate (mGlu) receptors also have a widespread distribution outside the central nervous system (CNS). In particular, group III mGlu receptors have been recently found in human stomach and colon revealing an extraordinary potential for these receptors in the treatment of peripheral disorders, including gastrointestinal dysfunction. The significance of these findings is that pharmacological tools originally designed for mGlu receptors in the CNS may also be directed towards new disease targets in the periphery. Targeting mGlu receptors can also be beneficial in the treatment of disorders involving central components together with gastrointestinal dysfunction, such as irritable bowel syndrome, which can be co-morbid with anxiety and depression. Conversely, the development of more specific therapeutic approaches for mGlu ligands both centrally as in the gut will depend on the elucidation of tissue-specific elements in mGlu receptor signalling.
AB - l-glutamate is produced by a great variety of peripheral tissues in both health and disease. Like other components of the glutamatergic system, metabotropic glutamate (mGlu) receptors also have a widespread distribution outside the central nervous system (CNS). In particular, group III mGlu receptors have been recently found in human stomach and colon revealing an extraordinary potential for these receptors in the treatment of peripheral disorders, including gastrointestinal dysfunction. The significance of these findings is that pharmacological tools originally designed for mGlu receptors in the CNS may also be directed towards new disease targets in the periphery. Targeting mGlu receptors can also be beneficial in the treatment of disorders involving central components together with gastrointestinal dysfunction, such as irritable bowel syndrome, which can be co-morbid with anxiety and depression. Conversely, the development of more specific therapeutic approaches for mGlu ligands both centrally as in the gut will depend on the elucidation of tissue-specific elements in mGlu receptor signalling.
KW - Brain-gut axis
KW - Gastrointestinal tract
KW - Metabotropic glutamate receptor
KW - Mood
UR - http://www.scopus.com/inward/record.url?scp=84871926883&partnerID=8YFLogxK
U2 - 10.1016/j.ejphar.2012.10.027
DO - 10.1016/j.ejphar.2012.10.027
M3 - Review article
C2 - 23123053
AN - SCOPUS:84871926883
SN - 0014-2999
VL - 698
SP - 19
EP - 30
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
IS - 1-3
ER -