Segmental Difference in Vasoreactivity of the Human Right Gastroepiploic Artery

Circ J. 2018 Feb 23;82(3):914-918. doi: 10.1253/circj.CJ-17-0943. Epub 2017 Dec 13.

Abstract

Background: The gastroepiploic artery (GEA) plays an important role in the era of multiple arterial revascularization, but spasm is a major matter of concern. The internal thoracic artery has been shown to have a strong tendency to spasm in its distal bifurcating part, whereas the segmental difference in vasoreactivity of the GEA has never been performed.Methods and Results:The full length of the GEA obtained from 21 patients undergoing a total gastrectomy was divided into 3 sections: proximal (5 cm from the origin), middle, and distal (5 cm from the end). Concentration-response curves for vasoconstrictors (phenylephrine, prostaglandin F2α, and endothelin-1) and vasodilators (carperitide, nitroglycerin, and nifedipine) were then established using organ baths. All the vasoconstrictors and vasodilators produced concentration-dependent responses in each section. As the concentration of the vasoconstrictors increased, segments at the distal section showed a significantly greater contraction than those at the middle and proximal sections regardless of the type of vasoconstrictor. The effective concentration of drugs that caused 50% of the maximal response for endothelin-1 was significantly greater in the distal section than that in the proximal sections. No significant difference was found in vasodilators-induced relaxation.

Conclusions: The contractility increases toward to the end of the GEA. Clinically, the distal portion of the GEA should be trimmed off and not be used as an anastomotic site wherever possible.

Keywords: Gastroepiploic artery; Internal thoraric artery; Spasm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dinoprost / pharmacology
  • Dose-Response Relationship, Drug
  • Endothelin-1 / pharmacology
  • Gastroepiploic Artery / physiology*
  • Humans
  • Phenylephrine / pharmacology
  • Vasoconstriction / drug effects*
  • Vasoconstriction / physiology
  • Vasoconstrictor Agents / pharmacology*

Substances

  • Endothelin-1
  • Vasoconstrictor Agents
  • Phenylephrine
  • Dinoprost