Hypothermia slows sequential and parallel steps initiated during caerulein pancreatitis

Pancreatology. 2014 Nov-Dec;14(6):459-64. doi: 10.1016/j.pan.2014.06.006. Epub 2014 Jul 3.

Abstract

Background and objectives: Multiple deleterious signaling cascades are simultaneously activated in acute pancreatitis (AP), which may limit the success of pharmacologic approaches targeting a single step. We explored whether cooling acinar cells slows distinct steps initiated from a stimulus causing pancreatitis simultaneously, and the temperature range over which inhibition of such deleterious signaling occurs.

Methods: Caerulein (100 nM) induced trypsinogen activation (TGA), CXCL1, CXCL2 mRNA levels, cell injury were studied at 37 °C, 34 °C, 31 °C, 29 °C and 25 °C in acinar cells. Trypsin, cathepsin B activities and cathepsin B mediated TGA were studied at 37 °C, 23 °C and 4 °C.

Results: There was >80% reduction in TGA, CXCL1 and CXCL2 mRNA levels at 29 °C, and in cell injury at 34 °C, compared to those at 37 °C. Trypsin activity, cathepsin B activity and cathepsin B mediated TGA at 23 °C were respectively, 53%, 64% and 26% of that at 37 °C. Acinar cooling to 31 °C reduced LDH leakage even when cooling was initiated an hour after caerulein stimulation at 37 °C.

Conclusions: Hypothermia synergistically and simultaneously slows parallel and distinct signaling steps initiated by caerulein, thereby reducing TGA, upregulation of inflammatory mediators and acinar injury.

Keywords: Acinar injury; Acute pancreatitis; Caerulein; Hypothermia; Inflammatory mediators; Trypsinogen activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acinar Cells
  • Activation, Metabolic / drug effects
  • Animals
  • Cathepsins / blood
  • Cell Death
  • Ceruletide / metabolism*
  • Chemokine CXCL1 / metabolism
  • Chemokine CXCL2 / metabolism
  • Disease Progression
  • Hypothermia, Induced / methods*
  • Mice
  • Mice, Inbred ICR
  • Pancreatitis / metabolism*
  • Pancreatitis / therapy*
  • Signal Transduction
  • Trypsin / metabolism
  • Trypsinogen / metabolism

Substances

  • Chemokine CXCL1
  • Chemokine CXCL2
  • Ceruletide
  • Trypsinogen
  • Cathepsins
  • Trypsin