Glucagon-like peptide-2 modulates neurally evoked mucosal chloride secretion in guinea pig small intestine in vitro

被引:38
作者
Baldassano, Sara [1 ]
Liu, Sumei [1 ,2 ]
Qu, Mei-Hu [1 ]
Mule, Flavia [1 ]
Wood, Jackie D. [1 ,2 ]
机构
[1] Ohio State Univ, Coll Med, Dept Physiol & Cell Biol, Columbus, OH 43210 USA
[2] Ohio State Univ, Coll Med, Dept Internal Med, Columbus, OH 43210 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2009年 / 297卷 / 04期
关键词
enteric nervous system; gastrointestinal hormones; intestine; mucosal secretion; GASTRIC-ACID-SECRETION; BARRIER FUNCTION; ENTERIC NEURONS; BLOOD-FLOW; GROWTH; STIMULATION; RECEPTORS; HUMANS; COLON; MICE;
D O I
10.1152/ajpgi.00170.2009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Baldassano S, Liu S, Qu M, Mule F, Wood JD. Glucagon-like peptide-2 modulates neurally evoked mucosal chloride secretion in guinea pig small intestine in vitro. Am J Physiol Gastrointest Liver Physiol 297: G800-G805, 2009. First published July 23, 2009; doi: 10.1152/ajpgi.00170.2009.-Glucagon-like peptide-2 (GLP-2) is an important neuroendocrine peptide in intestinal physiology. It influences digestion, absorption, epithelial growth, motility, and blood flow. We studied involvement of GLP-2 in intestinal mucosal secretory behavior. Submucosal-mucosal preparations from guinea pig ileum were mounted in Ussing chambers for measurement of short-circuit current (I-sc) as a surrogate for chloride secretion. GLP-2 action on neuronal release of acetylcholine was determined with ELISA. Enteric neuronal expression of the GLP-2 receptor (GLP-2R) was studied with immunohistochemical methods. Application of GLP-2 (0.1-100 nM) to the serosal or mucosal side of the preparations evoked no change in baseline I-sc and did not alter transepithelial ionic conductance. Transmural electrical field stimulation (EFS) evoked characteristic biphasic increases in I-sc, with an initially rapid rising phase followed by a sustained phase. Application of GLP-2 reduced the EFS-evoked biphasic responses in a concentration-dependent manner. The GLP-2R antagonist GLP-2-(3-33) significantly reversed suppression of the EFS-evoked responses by GLP-2. Tetrodotoxin, scopolamine, and hexamethonium, but not vasoactive intestinal peptide type 1 receptor (VPAC1) antagonist abolished or reduced to near zero the EFS-evoked responses. GLP-2 suppressed EFS-evoked acetylcholine release as measured by ELISA. Pretreatment with GLP-2(3-33) offset this action of GLP-2. In the submucosal plexus, GLP-2R immunoreactivity (-IR) was expressed in choline acetyltransferase-IR neurons, somatostatin-IR neurons, neuropeptide Y-IR neurons, and vasoactive intestinal peptide-IR neurons. We conclude that submucosal neurons in the guinea pig ileum express GLP-2R. Activation of GLP-2R decreases neuronally evoked epithelial chloride secretion by suppressing acetylcholine release from secretomotor neurons.
引用
收藏
页码:G800 / G805
页数:6
相关论文
共 36 条
[1]   Glucagon-like peptide-2 relaxes mouse stomach through vasoactive intestinal peptide release [J].
Amato, Antonella ;
Baldassano, Sara ;
Serio, Rosa ;
Mule, Flavia .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2009, 296 (03) :G678-G684
[2]   Glucagon-like peptide-2 enhances intestinal epithelial barrier function of both transcellular and paracellular pathways in the mouse [J].
Benjamin, MA ;
McKay, DM ;
Yang, PC ;
Cameron, H ;
Perdue, MH .
GUT, 2000, 47 (01) :112-119
[3]   Modulation of specific intestinal epithelial progenitors by enteric neurons [J].
Bjerknes, M ;
Cheng, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (22) :12497-12502
[4]   Intestinal function in mice with small bowel growth induced by glucagon-like peptide-2 [J].
Brubaker, PL ;
Izzo, A ;
Hill, M ;
Drucker, DJ .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (06) :E1050-E1058
[5]   Stress impairs murine intestinal barrier function: Improvement by glucagon-like peptide-2 [J].
Cameron, HL ;
Perdue, MH .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 314 (01) :214-220
[6]   Glucagon-like peptide-2-enhanced barrier function reduces pathophysiology in a model of food allergy [J].
Cameron, HL ;
Yang, PC ;
Perdue, MH .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 284 (06) :G905-G912
[7]  
Cooke HJ, 2006, PHYSIOLOGY OF THE GASTROINTESTINAL TRACT, VOLS 1 AND 2, 4TH EDITION, P737
[8]   EFFECTS OF NEURONAL STIMULATION ON MUCOSAL TRANSPORT IN GUINEA-PIG ILEUM [J].
COOKE, HJ ;
SHONNARD, K ;
WOOD, JD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1983, 245 (02) :G290-G296
[9]   VASOACTIVE INTESTINAL POLYPEPTIDE ACTIONS ON THE GUINEA-PIG INTESTINAL-MUCOSA DURING NEURAL STIMULATION [J].
COOKE, HJ ;
ZAFIROVA, M ;
CAREY, HV ;
WALSH, JH ;
GRIDER, J .
GASTROENTEROLOGY, 1987, 92 (02) :361-370
[10]   Mediators of glucagon-like peptide 2-induced blood flow: Responses in different vascular sites [J].
Deniz, Mustafa ;
Bozkurt, Ayhan ;
Kurtel, Hizir .
REGULATORY PEPTIDES, 2007, 142 (1-2) :7-15