The long term objective is to provide a quantitative understanding of the myogenic and neurogenic processes which regulate gastrointestinal smooth muscle activity in experimental animals and in man. Smooth muscle from the internal anal sphincter, ileocolonic/ileocecal sphincter, muscularis mucosa of the esophagus, small and large intestines and the inner and outer circular muscle lamellae will be used. The areas of particular interest are: (1) the electrophysiological properties of the smooth muscle cell membrane in each of these areas; (2) the electrophysiological characteristics of neuroeffector responses; (3) the pattern of intramural innervation; (4) the identity of the neurotransmitters which cause excitation and inhibition; and (5) the electrophysiological and neurotransmission processes in normal and diseased human GI smooth muscle. The methods of approach will involve recording simultaneously mechanical and intracellular electrical activity, the recording of contractility of strips of muscle, radio-immunoassay of muscle to identify the type and content of peptides and radio-immunological and immunological techniques to identify the excitatory and inhibitiory transmitters. In vitro studies are planned. Dogs, cats, rabbits, guinea pigs and human GI smooth muscle will be used. These studies may be particularly relevant to understanding motor disturbances involving hypoganglionosis of the intrinsic plexuses in man. They man also be relevant to disturbances in anal continence in man.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK017238-26
Application #
2838033
Study Section
General Medicine A Subcommittee 2 (GMA)
Program Officer
Hamilton, Frank A
Project Start
1976-12-01
Project End
2001-11-30
Budget Start
1998-12-01
Budget End
1999-11-30
Support Year
26
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
Sha, L; Linden, D R; Farrugia, G et al. (2014) Effect of endogenous hydrogen sulfide on the transwall gradient of the mouse colon circular smooth muscle. J Physiol 592:1077-89
Farrugia, Gianrico; Szurszewski, Joseph H (2014) Carbon monoxide, hydrogen sulfide, and nitric oxide as signaling molecules in the gastrointestinal tract. Gastroenterology 147:303-13
Sha, Lei; Linden, David R; Farrugia, Gianrico et al. (2013) Hydrogen sulfide selectively potentiates central preganglionic fast nicotinic synaptic input in mouse superior mesenteric ganglion. J Neurosci 33:12638-46
Linden, D R; Furne, J; Stoltz, G J et al. (2012) Sulphide quinone reductase contributes to hydrogen sulphide metabolism in murine peripheral tissues but not in the CNS. Br J Pharmacol 165:2178-90
Strege, Peter R; Bernard, Cheryl E; Kraichely, Robert E et al. (2011) Hydrogen sulfide is a partially redox-independent activator of the human jejunum Na+ channel, Nav1.5. Am J Physiol Gastrointest Liver Physiol 300:G1105-14
Linden, David R; Levitt, Michael D; Farrugia, Gianrico et al. (2010) Endogenous production of H2S in the gastrointestinal tract: still in search of a physiologic function. Antioxid Redox Signal 12:1135-46
Matsuda, Nilce Mitiko; Miller, Steven M; Szurszewski, Joseph H (2010) Heme-oxygenase-2 immunolabelling in pig jejunum. Acta Histochem 112:402-6
Sha, L; Farrugia, G; Linden, D R et al. (2010) The transwall gradient across the mouse colonic circular muscle layer is carbon monoxide dependent. FASEB J 24:3840-9
Fidler, J; Bharucha, A E; Camilleri, M et al. (2009) Application of magnetic resonance imaging to measure fasting and postprandial volumes in humans. Neurogastroenterol Motil 21:42-51
Linden, David R; Sha, Lei; Mazzone, Amelia et al. (2008) Production of the gaseous signal molecule hydrogen sulfide in mouse tissues. J Neurochem 106:1577-85

Showing the most recent 10 out of 71 publications