Effect of portosystemic shunting on PGl2 and glucagon levels in humans

James V. Sitzmann, Kurtis A. Campbell, Yuping Wu, John L. Cameron

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


Objective: This study determined if the proposed mediators of splanchnic blood flow, prostacyclin and glucagon, were elevated in patients with portal hypertension undergoing portal systemic shunts. Summary Background Data: Chronic portal hypertension results in increased portal venous pressure and increased splanchnic blood flow. Animal studies have suggested prostacyclin or glucagon, potent vasodilators, as potential mediators of this increased flow. Correlative clinical studies have been difficult to perform due to the wide variation in degree of portal-systemic shunting and the frequent association of parenchymal liver disease in patients with cirrhosis. Methods: The authors measured portal and systemic hemodynamics in PGl2 and glucagon levels in patients with portal hypertension due to cirrhosis (partial portal systemic shunt) and Budd-Chiari syndrome (complete portal systemic shunt) undergoing portal systemic shunts and in porto normotensive patients undergoing exploratory laparotomies. Results: PGl2 levels in portal hypertension were significantly increased over normal, and prostacyclin in Budd-Chiari patients were increased significantly over patients with cirrhosis. Both PGl2 and portal venous pressure decreased significantly after portal systemic shunting, and prostacyclin levels correlated directly with portal venous pressure (R = 0.37, p < 0.05). Conclusions: This is the first evidence in humans supporting the hypothesis that PGl2 is elevated in portal hypertension and is related to both the degree of portal venous obstruction and portal pressure. PGl2 probably has a role in the abnormal splanchnic hemodynamics of human portal hypertension.

Original languageEnglish (US)
Pages (from-to)248-252
Number of pages5
JournalAnnals of surgery
Issue number3
StatePublished - Mar 1993

ASJC Scopus subject areas

  • Surgery


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