This application represents a systematic detailed study of three important neuropeptide systems involved in regulation of the digestive system and other visceral organs. The investigations will focus on opioid peptides, tachykinins (substance P, substance K and others), and cholecystokinin (CCK). Emphasis throughout is on understanding of neuropeptide mechanisms of action relevant to their pharmacological effects, physiological roles, and biochemical characteristics. The central hypothesis is that neuropeptides function in both sensory and motor pathways in the brain, spinal cord and periphery to regulate physiological activity of the gastrointestinal tract, urinary bladder, blood vessels, and other visceral organs. The specific regulatory events initiated or modulated by individual neuropeptides reflect neurotransmitter actions at multiple receptor subtypes in multiple anatomical sites mediated by multiple molecular forms and involving multiple interactions with other regulatory substances. Because of the complexities of the neuropeptide actions and interactions, a comprehensive research program is required that simultaneously addresses mechanisms at multiple biological levels and employs multiple experimental approaches. Even with a large collaborative effort, not all peptides can be studied at once. We will focus on three specific peptide groups (opioids, tachykinins and CCK) thought to be involved in both sensory and motor components of visceral reflex pathways. Opioid peptides were chosen because they are known to exert powerful regulatory effects on gastrointestinal and bladder motility by actions at brain, spinal cord and intramural sites and because an array of pharmacological tools in available for their study (Table 1). Tachykinins are known to function in both sensory and motor pathways and to interact at multiple levels with opioid systems. Cholesystokinin (CCK) is heavily represented in sensory and motor pathways relevant to the gut and also appears to interact in specific ways with opioid systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK036289-05
Application #
3095401
Study Section
Special Emphasis Panel (SRC)
Project Start
1986-01-01
Project End
1991-12-31
Budget Start
1990-01-01
Budget End
1991-12-31
Support Year
5
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Arizona
Department
Type
Schools of Medicine
DUNS #
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Li, Y; Duckles, S P (1993) Effect of age on vascular content of calcitonin gene-related peptide and mesenteric vasodilator nerve activity in the rat. Eur J Pharmacol 236:373-8
Li, Y J; Duckles, S P (1992) Effect of endothelium on the actions of sympathetic and sensory nerves in the perfused rat mesentery. Eur J Pharmacol 210:23-30
Friedman, D J; Krause, D N; Duckles, S P (1992) Complex prejunctional actions of the D2 dopamine agonists N-0923 and N-0924 in the rat tail artery. J Pharmacol Exp Ther 260:568-75
Massamiri, T; Duckles, S P (1991) Sigma receptor ligands inhibit rat tail artery contractile responses by multiple mechanisms. J Pharmacol Exp Ther 259:22-9
Nguyen, K; Barrios, V; Duckles, S P (1991) Prejunctional effects of opioids in the perfused mesentery of the rat and rabbit: interactions with alpha 2-adrenoceptors. Life Sci 48:931-8
Li, Y J; Duckles, S P (1991) Effect of opioid receptor antagonists on vasodilator nerve actions in the perfused rat mesentery. Eur J Pharmacol 204:323-8
Li, Y J; Duckles, S P (1991) GABA agonists and omega conotoxin GVIA modulate responses to nerve activation of the perfused rat mesentery. Life Sci 48:2331-9
Massamiri, T; Duckles, S P (1991) Interactions of sigma and phencyclidine receptor ligands with the norepinephrine uptake carrier in both rat brain and rat tail artery. J Pharmacol Exp Ther 256:519-24
Li, Y J; Duckles, S P (1991) Differential effects of neuropeptide Y and opioids on neurogenic responses of the perfused rat mesentery. Eur J Pharmacol 195:365-72
Massamiri, T; Duckles, S P (1990) Multiple sites of action of (+)-3-(3-hydroxyphenyl)-N-(1-propyl)piperidine ((+)-3PPP) in blood vessels. Eur J Pharmacol 190:295-303

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