The goal of this project is to define the role of endogeneous prostaglandins in the control of gastric and intestinal motility. General questions under investigation will be: 1) Which prostaglandins are synthesized in physiologically significant concentrations? 2) What stimuli alter prostaglandin biosynthesis, 3) what are the mechanical consequences of endogeneous prostaglandins, 4) what are the electrophysiological mechanisms of the motor effects of prostaglandins. Prostaglandins probably function as local regulatory compounds, which means their synthesis, effect and deactivation must all occur locally, within the tissue. Therefore, the questions above will be studied with an in vitro, canine smooth muscle preparation. This proposal is unique because it will combine several well-known techniques to produce a unified picture of prostaglandin physiology. Microsomal preparations of muscle will be used to determine the types of prostaglandins the muscles are capable of producing. Radioimmunoassay (RIA) of muscle extracts will be used to measure basal prostaglandin levels and quantitate relative changes in prostaglandin concentration in response to various stimuli. Mechanical and intracellular electrical measurements will be made to isolate common aspects of stimuli which enhance prostaglandin synthesis, to determine the influence of endogenous prostaglandins and electrical and mechanical activities, and to determine the mechanism of the electrical and mechanical effects of prostaglandins. In parallel experiments normal and malfunctioning human gastric and intestinal muscles removed during corrective GI surgery will be studied. The techniques above will be applied in these studies to test the hypothesis that some pseudo-obstruction disorders are related to an over-abundance of endogenous prostaglandin.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK032176-06
Application #
3230623
Study Section
(GCN)
Project Start
1982-09-01
Project End
1989-03-31
Budget Start
1987-09-01
Budget End
1989-03-31
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Nevada Reno
Department
Type
Schools of Medicine
DUNS #
146515460
City
Reno
State
NV
Country
United States
Zip Code
89557
Stevens, R J; Weinert, J S; Publicover, N G (1999) Visualization of origins and propagation of excitation in canine gastric smooth muscle. Am J Physiol 277:C448-60
Frey, B W; Carl, A; Publicover, N G (1998) Charybdotoxin block of Ca(2+)-activated K+ channels in colonic muscle depends on membrane potential dynamics. Am J Physiol 274:C673-80
Burke, E P; Gerthoffer, W T; Sanders, K M et al. (1996) Wortmannin inhibits contraction without altering electrical activity in canine gastric smooth muscle. Am J Physiol 270:C1405-12
Sanders, K M; Publicover, N G (1994) Excitation-contraction coupling in gastric muscles. Dig Dis Sci 39:69S-72S
Sato, K; Sanders, K M; Gerthoffer, W T et al. (1994) Sources of calcium utilized in cholinergic responses in canine colonic smooth muscle. Am J Physiol 267:C1666-73
Publicover, N G; Hammond, E M; Sanders, K M (1993) Amplification of nitric oxide signaling by interstitial cells isolated from canine colon. Proc Natl Acad Sci U S A 90:2087-91
Ozaki, H; Gerthoffer, W T; Hori, M et al. (1993) Ca2+ regulation of the contractile apparatus in canine gastric smooth muscle. J Physiol 460:33-50
Ozaki, H; Zhang, L; Buxton, I L et al. (1992) Negative-feedback regulation of excitation-contraction coupling in gastric smooth muscle. Am J Physiol 263:C1160-71
Ozaki, H; Blondfield, D P; Hori, M et al. (1992) Cyclic AMP-mediated regulation of excitation-contraction coupling in canine gastric smooth muscle. J Physiol 447:351-72
Ozaki, H; Blondfield, D P; Hori, M et al. (1992) Spontaneous release of nitric oxide inhibits electrical, Ca2+ and mechanical transients in canine gastric smooth muscle. J Physiol 445:231-47

Showing the most recent 10 out of 23 publications