The propulsion of intestinal contents is dependent on the coordination of contraction and relaxation of the circular and longitudinal muscle of the gut. Our previous studies have examined in detail the peristaltic reflex which underlies propulsive activity, and have resulted in a model of the neuronal circuit that mediates this reflex in rat, guinea pig and human. Our recent studies have expanded the model by identifying the modulatory roles of NPY and GRP in ascending and descending pathways, by characterizing the sensory limb activated by chemical stimulation of the mucosa with short chain fatty acids, and by identifying the influence of inflammatory cytokines on the reflex. The model of the peristaltic reflex has been fully validated in the mouse colon, allowing us to use a variety of transgenic mice in each aim listed below. In the current proposal, we will examine two novel endogenous regulators of neural function: the neurotrophins BDNF and GDNF, and the endocannabinoids.
The first aim i s to characterize the physiological role of BDNF in modulating the sensory limb of the peristaltic reflex and to examine the autocrine and paracrine mechanisms by which BDNF acts to enhance the release of the sensory neurotransmitter, CGRP. The receptor type(s) and signaling pathways that mediate the actions of BDNF will be determined.
The second aim will characterize the role of GDNF and Neurturin in regulating the motor limb of the peristaltic reflex by examining their effect on motor and modulatory neurotransmitters.
The third aim will characterize the role of the endocannabinoids in modulating the sensory and motor limbs of the peristaltic reflex. The release of endocannabinoids during each phase of the reflex, the relative roles of the C, B-1 and VR-1 receptors in mediating the response to endocannabinoids, and the interaction between endocannabinoids and neurotrophins will be determined. We have done extensive preliminary studies in support of these three aims, and their completion will enhance our understanding of the peristaltic reflex.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK034153-24
Application #
7276077
Study Section
Clinical and Integrative Gastrointestinal Pathobiology Study Section (CIGP)
Program Officer
May, Michael K
Project Start
1984-07-01
Project End
2009-08-31
Budget Start
2007-09-01
Budget End
2008-08-31
Support Year
24
Fiscal Year
2007
Total Cost
$270,231
Indirect Cost
Name
Virginia Commonwealth University
Department
Physiology
Type
Schools of Medicine
DUNS #
105300446
City
Richmond
State
VA
Country
United States
Zip Code
23298
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