Effect of a selective chloride channel activator, lubiprostone, on gastrointestinal transit, gastric sensory, and motor functions in healthy volunteers

• Published in: American journal of physiology: Gastrointestinal and liver physiology Vol. 290; no. 5; pp. G942 - G947
• Main Authors: Camilleri, Michael, Bharucha, Adil E, Ueno, Ryuji, Burton, Duane, Thomforde, George M, Baxter, Kari, McKinzie, Sanna, Zinsmeister, Alan R
• Format: Journal Article
• Language: English
• Published: United States 01.05.2006
• Subjects: Adolescent; Adult; Alprostadil - adverse effects; Alprostadil - analogs & derivatives; Alprostadil - pharmacology; Chloride Channels - physiology; Double-Blind Method; Fatty Acids - adverse effects; Fatty Acids - pharmacology; Female; Gastric Emptying - drug effects; Gastrointestinal Transit - drug effects; Humans; Lubiprostone; Male; Middle Aged; Placebos; Stomach - physiology
• ISSN: 0193-1857; 1522-1547
• DOI: 10.1152/ajpgi.00264.2005

Chloride channels modulate gastrointestinal neuromuscular functions in vitro. Lubiprostone, a selective type 2 chloride channel (ClC-2) activator, induces intestinal secretion and has been shown to relieve constipation in clinical trials; however, the effects of lubiprostone on gastric function and whole gut transit in humans are unclear. Our aim was to compare the effects of the selective ClC-2 activator lubiprostone on maximum tolerated volume (MTV) of a meal, postprandial symptoms, gastric volumes, and gastrointestinal and colonic transit in humans. We performed a randomized, parallel-group, double-blind, placebo-controlled study evaluating the effects of lubiprostone (24 microg bid) in 30 healthy volunteers. Validated methods were used: scintigraphic gastrointestinal and colonic transit, SPECT to measure gastric volumes, and the nutrient drink ("satiation") test to measure MTV and postprandial symptoms. Lubiprostone accelerated small bowel and colonic transit, increased fasting gastric volume, and retarded gastric emptying. MTV values were reduced compared with placebo; however, the MTV was within the normal range for healthy adults in 13 of 14 participants, and there was no significant change compared with baseline measurements. Lubiprostone had no significant effect on postprandial gastric volume or aggregate symptoms but did decrease fullness 30 min after the fully satiating meal. Thus the ClC-2 activator lubiprostone accelerates small intestinal and colonic transit, which confers potential in the treatment of constipation.