Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Sep;29(5):517-22.
doi: 10.1097/MOG.0b013e3283639326.

Modulation of pancreatic exocrine and endocrine secretion

Affiliations
Review

Modulation of pancreatic exocrine and endocrine secretion

Rashmi Chandra et al. Curr Opin Gastroenterol. 2013 Sep.

Abstract

Purpose of review: Recent advances in the regulation of pancreatic secretion by secretagogues, modulatory proteins and neural pathways are discussed.

Recent findings: Downstream events involved in secretagogue stimulation of pancreatic secretion have been elucidated through characterization of the Src kinase pathway. An additional mechanism regulating vagus nerve effects on the pancreas involves Group II and III metabotropic glutamate receptors that are located presynaptically on certain vagal pancreas-projecting neurons. Hypothalamic neurons perceive glucose and regulate insulin release by direct communication with islets, and activation of proopiomelanocortin neurons by leptin enhances insulin secretion and modulates glucose but not energy homeostasis. Ghrelin and somatostatin mediate glucose-stimulated insulin secretion by differential receptor signaling that is dependent on the amount of ghrelin and state of receptor heterodimerization. Endoplasmic reticulum (ER) stress and loss-of-function mutations of a key ER stress protein are associated with disruption of membrane translocation and reduction in insulin secretion. The importance of hormones, neuropeptides, amino acids, cytokines and regulatory proteins in pancreatic secretion and the pathophysiology of type 2 diabetes are also discussed.

Summary: The biomolecular pathways regulating pancreatic secretions are still not fully understood. New secretagogues and mechanisms continue to be identified and this information will aid in drug discovery and development of new and improved therapy for pancreatic disorders.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflict of interest.

References

    1. Petrella C, Broccardo M, Possenti R, et al. TLQP-21, a VGF-derived peptide, stimulates exocrine pancreatic secretion in the rat. Peptides. 2012;36:133–136. This is the first study to show that a VGF peptide stimulates exocrine secretion from pancreatic lobules through a prostaglandin-mediated pathway. - PubMed
    1. Cassina V, Torsello A, Tempestini A, et al. Biophysical characterization of a binding site for TLQP-21, a naturally occurring peptide which induces resistance to obesity. Biochim Biophys Acta. 2013;1828:455–460. This paper demonstrates that TLQP-21 interacts with as yet unidentified receptors on Chinese hamster ovary cells and binding is associated with mobilization of intracellular calcium. - PubMed
    1. Sancho V, Nuche-Berenguer B, Jensen RT. The Src kinase Yes is activated in pancreatic acinar cells by gastrointestinal hormones/neurotransmitters, but not pancreatic growth factors, which stimulate its association with numerous other signaling molecules. Biochim Biophys Acta - Molecular Cell Research. 2012;1823:1285–1294. In acinar cells, Src kinase Yes is activated by secretagogues such as CCK, and plays an important role in cellular signaling. - PMC - PubMed
    1. Rakonczay Z, Jr, Hegyi P, Takacs T, et al. The role of NF-kappaB activation in the pathogenesis of acute pancreatitis. Gut. 2008;57:259–267. - PubMed
    1. Ma B, Wu L, Lu M, et al. Differentially expressed kinase genes associated with trypsinogen activation in rat pancreatic acinar cells treated with taurolithocholic acid 3-sulfate. Molecular medicine reports. 2013;7:1591–1596. Several kinases including Yes were upregulated in activated AR42J cells suggesting a role for these kinases in the pathophysiology of acute pancreatitis. - PubMed

MeSH terms