Presence of putative neurotransmitters in the myenteric plexus of the gastrointestinal tract and in the musculature of the urinary bladder of the ferret

1998 ◽  
Vol 10 (1) ◽  
pp. 35-47 ◽  
Author(s):  
SANN ◽  
HOPPE ◽  
BALDWIN ◽  
GRUNDY ◽  
SCHEMANN
2008 ◽  
Vol 150 (1-3) ◽  
pp. 73-80 ◽  
Author(s):  
Shannon J. Raboin ◽  
Joseph R. Reeve ◽  
Marvis S. Cooper ◽  
Gary M. Green ◽  
Ayman I. Sayegh

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
David Grundmann ◽  
Markus Klotz ◽  
Holger Rabe ◽  
Matthias Glanemann ◽  
Karl-Herbert Schäfer

1989 ◽  
Vol 256 (5) ◽  
pp. G884-G896 ◽  
Author(s):  
T. Gonda ◽  
E. E. Daniel ◽  
T. J. McDonald ◽  
J. E. Fox ◽  
B. D. Brooks ◽  
...  

The distribution of nerves containing galanin-immunoreactive (GAL-IR) material was compared to the distribution of neurons containing vasoactive intestinal polypeptide (VIP) immunoreactivity in the canine gastrointestinal tract. The actions of intra-arterially administered galanin and VIP on motility in the gastric antrum and corpus and the intestines were also studied. All sphincter muscles contained galanin- and VIP-immunoreactive nerve profiles. VIP-immunoreactive nerve profiles were present in all layers of the stomach, small intestine, and colon. GAL-IR nerve somata were common in the submucous plexus of ileum and colon and in the myenteric plexus of the terminal antrum, as were nerve processes in various layers. In the small intestine, galanin inhibited contractile responses to field stimulation of intrinsic nerves and also reduced the contractions after nerve blockade with tetrodotoxin (TTX). VIP often enhanced field-stimulated contractions at low doses but inhibited these and the contractions after TTX at higher doses. In the stomach and colon, both peptides inhibited responses to field stimulation; whether these effects were due to actions on smooth muscle was not tested. The distribution and actions of galanin in gut are consistent with the hypothesis that it acts at smooth muscle sites and possibly at prejunctional sites.


1983 ◽  
Vol 85 (4) ◽  
pp. 890-899 ◽  
Author(s):  
James Christensen ◽  
Gary A. Rick ◽  
Bryce A. Robison ◽  
Michael J. Stiles ◽  
Mark A. Wix

PLoS ONE ◽  
2014 ◽  
Vol 9 (8) ◽  
pp. e103894 ◽  
Author(s):  
Hercules T. Maguma ◽  
Dipanjana Datta De ◽  
Sukhada Bhave ◽  
William L. Dewey ◽  
Hamid I. Akbarali

2012 ◽  
Vol 27 (3) ◽  
pp. 244-250 ◽  
Author(s):  
Sidney Pereira Pinto Lemos ◽  
José Luiz Martins ◽  
Patrícia Veruska Ribeiro Barbosa Lemos ◽  
Silvio Romero Gonçalves e Silva ◽  
Fernando Leandro dos Santos ◽  
...  

PURPOSE: The pathophysiology of abnormalities associated with myenteric plexus lesions remains imperfectly understood. Such abnormalities have been correlated with subocclusive intestinal conditions in children with Hirschsprung's disease, cases of chronic constipation and, postoperatively, in cases of anorectal anomalies. This study evaluated abnormalities of the myenteric plexus in fetus from female rats that received ethylenethiourea. METHODS: Female rats were exposed to ethylenethiourea on the 11th day of pregnancy (experimental group) or to 0.9% physiological solution (control group). Abnormalities were only found in the experimental group. The digestive tract muscle layer was analyzed morphometrically and changes to the frequencies of nerve plexus cells and interstitial cells of Cajal were evaluated, using hematoxylin-eosin, S-100 protein, neuron-specific enolase and C-Kit, respectively. RESULTS: Muscle and skeletal abnormalities were observed in 100%, anorectal anomalies in 86%, absent tail in 71%, short tail in 29%, duodenal atresia in 5%, esophageal atresia in 5% and persistent omphalomesenteric duct in 5%. Histopathological analysis showed a thinner muscle layer associated with lower frequencies of ganglion cells and interstitial cells of Cajal, in all gastrointestinal tract. CONCLUSION: Severe nerve plexus abnormalities associated with muscle layer atrophy were observed throughout the gastrointestinal tract in newborn rats exposed to ethylenethiourea.


2001 ◽  
Vol 281 (2) ◽  
pp. G533-G543 ◽  
Author(s):  
Y. F. Wang ◽  
E. E. Daniel

In the canine gastrointestinal tract, the roles that gap junctions play in pacemaking and neurotransmission are unclear. Using antibodies to connexin (Cx)43, Cx45, and Cx40, we determined the distribution of these connexins. Cx43 was present in all locations where structural gap junctions occur. Cx40 was also widely distributed in the circular muscle of the lower esophageal sphincter (LES), stomach, and ileum. Cx45 was sparsely distributed in circular muscle of the LES. In the interstitial cells of Cajal (ICC) networks of myenteric plexus, in the deep muscular and submuscular plexuses, sparse Cx45 and Cx40 immunoreactivity was present. In colon, immunoreactivity was found only in the myenteric and submuscular plexus and nearby circular muscle cells. No immunoreactivity was found in sites lacking structural gap junctions (longitudinal muscle, inner circular muscle of the intestine, and most circular muscle of the colon). Studies of colocalization of connexins suggested that in the ICC networks, some colocalization of Cx43 with Cx40 and/or Cx45 occurred. Thus gap junctions in canine intestine may be heterotypic or heteromeric and have different conductance properties in different regions based on different connexin compositions.


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