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The Physiology and Pathophysiology of Pancreatic Ductal Secretion The Background for Clinicians

Journal

PANCREAS
Volume 44, Issue 8, Pages 1211-1233

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MPA.0000000000000421

Keywords

pancreas; ductal secretion; cystic fibrosis; CFTR; pancreatitis; diabetes mellitus

Funding

  1. Hungarian National Development Agency [TAMOP-4.2.2.A-11/1/KONV-2012-0035, TAMOP-4.2.2-A-11/1/KONV-2012-0052, TAMOP-4.2.2.A-11/1/KONV-2012-0073]
  2. Hungarian Scientific Research Fund [NF105758]
  3. Hungarian Academy of Sciences (MTA-SZTE Momentum grant) [LP2014-10/2014]
  4. European Union
  5. State of Hungary
  6. European Social Fund National Excellence Program [TAMOP 4.2.4.A/2-11-1-2012-0001]

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The human exocrine pancreas consists of 2 main cell types: acinar and ductal cells. These exocrine cells interact closely to contribute to the secretion of pancreatic juice. The most important ion in terms of the pancreatic ductal secretion is HCO3-. In fact, duct cells produce an alkaline fluid that may contain up to 140 mM NaHCO3-, which is essential for normal digestion. This article provides an overviewof the basics of pancreatic ductal physiology and pathophysiology. In the first part of the article, we discuss the ductal electrolyte and fluid transporters and their regulation. The central role of cystic fibrosis transmembrane conductance regulator (CFTR) is highlighted, which is much more than just a Cl- channel. We also review the role of pancreatic ducts in severe debilitating diseases such as cystic fibrosis (caused by various genetic defects of cftr), pancreatitis, and diabetes mellitus. Stimulation of ductal secretion in cystic fibrosis and pancreatitis may have beneficial effects in their treatment.

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