Distorted microangioarchitecture and impaired angiogenesis in gastric mucosa of portal hypertensive rats

Gastroenterology. 1994 Mar;106(3):702-8. doi: 10.1016/0016-5085(94)90705-6.

Abstract

Background/aims: Portal hypertensive (PHT) gastropathy is now recognized as a distinct entity, but the size of microvessels has been a subject of controversy. Angiogenesis in PHT gastric mucosa has not been explored. The aim of this study was to examine the angioarchitecture of PHT and non-PHT gastric mucosae before and after ethanol-induced injury utilizing microvascular cast techniques.

Methods: Portal hypertension was produced by staged portal vein occlusion. Fourteen days later, gastric vascular casts were made in both PHT and control (sham-operated) rats by Mercox resin infusion. After tissue dissolution, casts were examined under a scanning electron microscope. To examine angiogenesis in injured gastric mucosa, the above study was repeated in PHT and control rats 18 hours after intragastric administration of 100% ethanol.

Results: The capillary casts in PHT gastric mucosa (mean diameter, 6.3 +/- 0.03 microns) were significantly narrower than those of controls (mean diameter, 8.6 +/- 0.02 microns; P < 0.01). After ethanol injury, 5.5% +/- 0.3% of microvessels in gastric mucosa of sham-operated rats contained buds, showing angiogenesis. In contrast, PHT gastric mucosa had a paucity of capillary angiogenesis (buds in only 0.4% +/- 0.2% of microvessels; P < 0.01 vs. control).

Conclusions: This study shows prominent persistent abnormalities in the microangioarchitecture of PHT gastric mucosa. Moreover, PHT gastric mucosal microvessels have a marked impairment of angiogenic response to ethanol injury.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Blood Vessels / drug effects
  • Blood Vessels / ultrastructure
  • Corrosion Casting
  • Ethanol / administration & dosage
  • Ethanol / pharmacology
  • Gastric Mucosa / blood supply*
  • Gastric Mucosa / drug effects
  • Hypertension, Portal / pathology*
  • Hypertension, Portal / physiopathology*
  • Male
  • Microcirculation / drug effects
  • Microscopy, Electron, Scanning
  • Neovascularization, Pathologic / pathology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Ethanol