Recent evidence indicates that peptide-containing neurons have crucial regulatory roles in nearly every aspect of digestive function. However, the mechanisms by which peptidergic neurons interact with the classical divisions of the autonomic nervous system are largely unknown. This lack of basic information is a major obstacle to rational treatment of human enteric autonomic disorders, and is reflected in the current empiric, and often ineffective, treatment of human neuropathic disease. The current research proposal is designed to investigate, on a fundamental level, the actions of selected pancreatic neuropeptides, chosen because they demonstrate reciprocal actions within the enteropancreatic nervous system. We have hypothesized that: 1) peptide neurotransmitters regulate pancreatic function by mechanisms that act directly on acinar cells and indirectly via modulation of cholinergic neurotransmission; 2) peptide neurotransmitters activate both membrane-bound and intracellular second messenger systems; 3) acetylcholine controls neural activity via membrane- associated calcium channels; and 4) neural function is regulated, at the transcriptional level, by neuropeptide-activated calcium signalling pathways. The proposed experiments integrate physiological studies with recent advances in cellular and molecular biology. It is hoped that these studies can serve as a paradigm for other investigations of neuropeptides that affect digestive function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK043225-04
Application #
2142859
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1991-01-01
Project End
1998-12-31
Budget Start
1994-01-01
Budget End
1994-12-31
Support Year
4
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Surgery
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Li, Ji-Yao; Chai, Biaoxin; Zhang, Weizhen et al. (2014) LGR4 and its ligands, R-spondin 1 and R-spondin 3, regulate food intake in the hypothalamus of male rats. Endocrinology 155:429-40
Fritze, Danielle; Zhang, Weizhen; Li, Ji-Yao et al. (2014) TNF? causes thrombin-dependent vagal neuron apoptosis in inflammatory bowel disease. J Gastrointest Surg 18:1632-41
Chai, B; Li, J-Y; Fritze, D et al. (2013) A novel transcript is up-regulated by fasting in the hypothalamus and enhances insulin signalling. J Neuroendocrinol 25:292-301
Xia, Ze-Feng; Fritze, Danielle M; Li, Ji-Yao et al. (2012) Nesfatin-1 inhibits gastric acid secretion via a central vagal mechanism in rats. Am J Physiol Gastrointest Liver Physiol 303:G570-7
Xu, G; Wang, Z; Li, Y et al. (2012) Ghrelin contributes to derangements of glucose metabolism induced by rapamycin in mice. Diabetologia 55:1813-23
Li, Ziru; Xu, Geyang; Li, Yin et al. (2012) mTOR-dependent modulation of gastric nesfatin-1/NUCB2. Cell Physiol Biochem 29:493-500
Wu, X; Zhang, W; Li, J-Y et al. (2011) Induction of apoptosis by thrombin in the cultured neurons of dorsal motor nucleus of the vagus. Neurogastroenterol Motil 23:279-85, e123-4
Li, Ji-Yao; Chai, Biao-Xin; Zhang, Weizhen et al. (2010) Expression of ankyrin repeat and suppressor of cytokine signaling box protein 4 (Asb-4) in proopiomelanocortin neurons of the arcuate nucleus of mice produces a hyperphagic, lean phenotype. Endocrinology 151:134-42
Xu, Geyang; Li, Yin; An, Wenjiao et al. (2010) Regulation of gastric hormones by systemic rapamycin. Peptides 31:2185-92
An, Wenjiao; Li, Yin; Xu, Geyang et al. (2010) Modulation of ghrelin O-acyltransferase expression in pancreatic islets. Cell Physiol Biochem 26:707-16

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