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Mucosal glucagon‐like peptide 1 ( GLP ‐1) responses are mediated by calcitonin gene‐related peptide ( CGRP ) in the mouse colon and both peptide responses are area‐specific
Author(s) -
Tough I.R.,
Moodaley R.,
Cox H.M.
Publication year - 2018
Publication title -
neurogastroenterology and motility
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.489
H-Index - 105
eISSN - 1365-2982
pISSN - 1350-1925
DOI - 10.1111/nmo.13149
Subject(s) - calcitonin gene related peptide , endocrinology , medicine , peptide yy , calcitonin , chemistry , receptor , agonist , glucagon like peptide 1 , glucagon like peptide 2 , enteroendocrine cell , peptide , neuropeptide , hormone , neuropeptide y receptor , biochemistry , endocrine system , type 2 diabetes , diabetes mellitus
Background Glucagon‐like peptide ( GLP )‐1 is an incretin hormone and its mimetics are proven antidiabetic and antiobesity drugs. GLP ‐1 exerts antimotility and mucosal proliferative activities but its epithelial ion transport effects are uncharacterized and these may contribute to the gastrointestinal ( GI ) disturbance, i.e., diarrhea experienced with some GLP ‐1 mimetics. Our aim was to establish GLP ‐1 agonist mechanisms and identify potential mucosal mediator(s) in the colonic tissue from C57BL/6J mice. Methods A tissue survey of GLP ‐1 responses (using exendin 4, Ex4) and α‐calcitonin gene‐related peptide (α CGRP ) was undertaken, dividing the mouse colon into eight adjacent mucosal‐submucosal preparations. Each preparation was voltage‐clamped and changes in short‐circuit current (Isc) measured. The involvement of submucosal neurons in GLP ‐1 agonism was tested using Ex(9‐39) and tetrodotoxin ( TTX ), and CGRP receptors were blocked with BIBN 4094. Key Results Ex4 responses along the length of the colon were inhibited by the GLP ‐1 antagonist, Ex(9‐39) or TTX , indicating neural mediation in all colonic regions. In the ascending colon, Ex4 increased Isc levels that were abolished by 10 nM BIBN 4096, while in the descending colon it reduced Isc levels that were again BIBN 4096‐sensitive, but at 1 μM. The latter α CGRP response was dependent on epithelial Cl − conductance and Na + /K + ‐ ATP ase, and was partially (~25%) peptide YY ‐mediated, but was not nitrergic, somatostatin sst 2 , or α 2 ‐adrenoceptor‐mediated. Conclusions and Inferences GLP ‐1 modulates epithelial ion transport indirectly by activating CGRP ‐containing submucosal enteric neurons in the mouse colon. This GLP ‐1‐ CGRP response was area‐specific and could potentially contribute to the diarrheal side effect of certain GLP ‐1R therapeutics.