Effect of experimental acalculous cholecystitis on gallbladder smooth muscle contractility

• Published in: Digestive diseases and sciences Vol. 44; no. 11; pp. 2235 - 2243
• Main Authors: PARKMAN, H. P, BOGAR, L. J, BARTULA, L. L, PAGANO, A. P, THOMAS, R. M, MYERS, S. I
• Format: Journal Article
• Language: English
• Published: Heidelberg Springer 01-11-1999; Springer Nature B.V
• Subjects: Animals; Bethanechol - pharmacology; Biological and medical sciences; Cholecystitis - etiology; Cholecystitis - physiopathology; Common Bile Duct - surgery; Gallbladder - physiopathology; Gallbladder Emptying - physiology; Gastroenterology. Liver. Pancreas. Abdomen; Guinea Pigs; Ligation; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Male; Medical sciences; Muscle Contraction - drug effects; Muscle Contraction - physiology; Muscle, Smooth - drug effects; Muscle, Smooth - physiopathology; Other diseases. Semiology; Potassium - pharmacology; Contractility; Smooth muscle; Inflammation; Biliary tract disease; Pig; Vertebrata; Experimental disease; Mammalia; Animal; Digestive diseases; Gallbladder; Artiodactyla; Biological effect; Cholecystitis; Ungulata
• ISSN: 0163-2116; 1573-2568
• DOI: 10.1023/A:1026600603121

Gallbladder motility is impaired in chronic cholelithiasis but has not been studied in acute acalculous cholecystitis. The aim of this study was to determine the effects of acute acalculous inflammation on gallbladder contractility using the common bile duct ligation (CBDL) model in guinea pigs. Three groups of guinea pigs were studied: CBDL, normal, and sham surgical controls. Gallbladder dimensions were measured, and muscle strips were used for histology and in vitro contractility studies. CBDL resulted in progressive gallbladder distension, increased serum bilirubin, and gallbladder inflammation. There was a progressive decline in muscle contractility in the CBDL group as evidenced by a decrease in the contractile response to potassium and bethanechol with the duration of CBDL. In conclusion, CBDL in the guinea pig produces acute gallbladder inflammation and decreased gallbladder muscle contractility. Direct inhibition of muscle function is indicated by impaired contractile responses to potassium depolarization and bethanechol stimulation. Although the mechanism of the decrease in contractility with CBDL is unknown, we speculate that impaired muscle contractility is secondary to inflammation and may play a role in the clinicopathology of acute acalculous cholecystitis.