Redefining the properties of an osmotic agent in an intestinal-specific preservation solution

World J Gastroenterol. 2010 Dec 7;16(45):5701-9. doi: 10.3748/wjg.v16.i45.5701.

Abstract

Aim: To investigate the effects of dextrans of various molecular weights (Mw) during a 12 h cold storage time-course on energetics, histology and mucosal infiltration of fluorescein isothiocyanate (FITC)-dextran.

Methods: Rodent intestines were isolated and received a standard University of Wisconsin vascular flush followed by intraluminal administration of a nutrient-rich preservation solution containing dextrans of varying Mw: Group D1, 73 kdal; Group D2, 276 kdal; Group D3, 534 kdal; Group D4, 1185 kdal; Group D5, 2400 kdal.

Results: Using FITC-labeled dextrans, fluorescent micrographs demonstrated varying degrees of mucosal infiltration; lower Mw (groups D1-D3: 73-534 kdal) dextrans penetrated the mucosa as early as 2 h, whereas the largest dextran (D5: 2400 kdal) remained captive within the lumen and exhibited no permeability even after 12 h. After 12 h, median injury grades ranged from 6.5 to 7.5 in groups D1-D4 (73-1185 kdal) representing injury of the regenerative cryptal regions and submucosa; this was in contrast to group D5 (2400 kdal) which exhibited villus denudation (with intact crypts) corresponding to a median injury grade of 4 (P < 0.05). Analysis of tissue energetics reflected a strong positive correlation between Mw and adenosine triphosphate (r(2) = 0.809), total adenylates (r(2) = 0.865) and energy charge (r(2) = 0.667).

Conclusion: Our data indicate that dextrans of Mw > 2400 kdal act as true impermeant agents during 12 h ischemic storage when incorporated into an intraluminal preservation solution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / chemistry
  • Adenosine / pharmacology
  • Adenosine Triphosphate / metabolism
  • Allopurinol / chemistry
  • Allopurinol / pharmacology
  • Animals
  • Cold Ischemia* / adverse effects
  • Dextrans / chemistry
  • Dextrans / metabolism
  • Dextrans / pharmacology*
  • Energy Metabolism
  • Fluorescein-5-isothiocyanate / analogs & derivatives
  • Fluorescein-5-isothiocyanate / metabolism
  • Glutathione / chemistry
  • Glutathione / pharmacology
  • Insulin / chemistry
  • Insulin / pharmacology
  • Intestinal Absorption
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Intestinal Mucosa / transplantation
  • Intestine, Small / drug effects*
  • Intestine, Small / metabolism
  • Intestine, Small / pathology
  • Intestine, Small / transplantation
  • Molecular Weight
  • Organ Preservation Solutions / chemistry
  • Organ Preservation Solutions / pharmacology*
  • Osmosis
  • Oxidative Stress / drug effects
  • Permeability
  • Raffinose / chemistry
  • Raffinose / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury / etiology
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology
  • Reperfusion Injury / prevention & control*
  • Time Factors

Substances

  • Dextrans
  • Insulin
  • Organ Preservation Solutions
  • University of Wisconsin-lactobionate solution
  • fluorescein isothiocyanate dextran
  • Allopurinol
  • Adenosine Triphosphate
  • Glutathione
  • Fluorescein-5-isothiocyanate
  • Adenosine
  • Raffinose