Role of cholinergic neurons in the motor effects of glucagon-like peptide-2 in mouse colon

被引:37
作者
Amato, Antonella
Rotondo, Alessandra
Cinci, Lorenzo [2 ]
Baldassano, Sara
Vannucchi, Maria Giuliana [2 ]
Mule, Flavia [1 ]
机构
[1] Univ Palermo, Lab Fisiol Gen, Dipartimento Biol Cellulare & Sviluppo, I-90128 Palermo, Italy
[2] Univ Florence, Dipartimento Anat Istol & Med Legale, Florence, Italy
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2010年 / 299卷 / 05期
关键词
enteric nervous system; gastrointestinal hormones; colonic motility; acetylcholine; DIVERGENT SIGNALING PATHWAYS; GLP-2; RECEPTOR; ENTERIC NEURONS; ACTIVATION; HUMANS; RAT; IDENTIFICATION; ABSORPTION; SECRETION; INTESTINE;
D O I
10.1152/ajpgi.00282.2010
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Amato A, Rotondo A, Cinci L, Baldassano S, Vannucchi MG, Mule F. Role of cholinergic neurons in the motor effects of glucagon-like peptide-2 in mouse colon. Am J Physiol Gastrointest Liver Physiol 299: G1038-G1044, 2010. First published August 12, 2010; doi: 10.1152/ajpgi.00282.2010.-Glucagon-like peptide-2 (GLP-2) reduces mouse gastric tone and small intestine transit, but its action on large intestine motility is still unknown. The purposes of the present study were 1) to examine the influence of GLP-2 on spontaneous mechanical activity and on neurally evoked responses, by recording intraluminal pressure from mouse isolated colonic segments; 2) to characterize GLP-2 mechanism of action; and 3) to determine the distribution of GLP-2 receptor (GLP-2R) in the mouse colonic muscle coat by immunohistochemistry. Exogenous GLP-2 (0.1-300 nM) induced a concentration-dependent reduction of the spontaneous mechanical activity, which was abolished by the desensitization of GLP-2 receptor or by tetrodotoxin, a voltage-dependent Na+-channel blocker. GLP-2 inhibitory effect was not affected by N-omega-nitro-L-arginine methyl ester (a nitric oxide synthase inhibitor), apamin (a blocker of small conductance Ca2+-dependent K+ channels), or [Lys1, Pro2,5, Arg3,4, Tyr6]VIP7-28 (a VIP receptor antagonist), but it was prevented by atropine or pertussis toxin (PTX), a G(i/o) protein inhibitor. Proximal colon responses to electrical field stimulation were characterized by nitrergic relaxation, which was followed by cholinergic contraction. GLP-2 reduced only the cholinergic evoked contractions. This effect was almost abolished by GLP-2 receptor desensitization or PTX. GLP-2 failed to affect the contractile responses to exogenous carbachol. GLP-2R immunoreactivity (IR) was detected only in the neuronal cells of both plexuses of the colonic muscle coat. More than 50% of myenteric GLP-2R-IR neurons shared the choline acetyltransferase IR. In conclusion, the activation of GLP-2R located on cholinergic neurons may modulate negatively the colonic spontaneous and electrically evoked contractions through inhibition of acetylcholine release. The effect is mediated by G(i) protein.
引用
收藏
页码:G1038 / G1044
页数:7
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