Biliary response to glucagon and insulin following hepatic transplantation in humans

Gene D. Branum, Bert A. Bowers, Christopher R. Watters, Giovanni Cucchiaro, William C. Meyers

Research output: Contribution to journalArticlepeer-review

4 Scopus citations


Glucagon and insulin are postulated to be physiologic regulators of hepatic biliary secretion. Effects of these hormones were studied following orthotopic transplantation. Five adult hepatic graft recipients had triple lumen t-tubes placed at the time of surgery and were studied 3 months after surgery. Experiments were performed after cholangiographic confirmation of t-tube placement and function. After overnight fast, t-tubes were inflated and bile was collected. A small quantity was saved for analysis and the remainder was reinfused to maintain enterohepatic circulation. After 1 hr of observation, the patients received a 2-hr infusion of insulin (0.125 U kg-1 hr-1), glucagon (2 μg kg-1 hr-1), or 0.9% saline. During saline infusions, all parameters remained stable. As has been previously demonstrated in the canine model and intact patients, bile salt outputs were constant under all experimental conditions. Glucagon stimulated bile secretion by 30% (6.7 ± 1.5 to 8.7 ± 1.2 ml/15 min) and inhibited biliary cholesterol output by 47% (16.4 ± 3.2 to 8.7 ± 1.5 mg/15 min). Bile flow and lipid secretion were not affected by insulin. Glucagon had profound effects on bile flow and lipid secretion, suggesting effects independent of innervation, while insulin at this dose had no statistically significant effects.

Original languageEnglish (US)
Pages (from-to)121-125
Number of pages5
JournalJournal of Surgical Research
Issue number2
StatePublished - Aug 1990
Externally publishedYes

ASJC Scopus subject areas

  • Surgery


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