Review article: in vitro studies of gall-bladder smooth muscle function. Relevance in cholesterol gallstone disease

被引:9
作者
Portincasa, P
Minerva, F
Moschetta, A
Venneman, N
Vanberge-Henegouwen, GP
Palasciano, G
机构
[1] Univ Bari, Sch Med, Dept Internal Med & Publ Hlth, Sect Internal Med, I-70124 Bari, Italy
[2] Univ Utrecht Hosp, Dept Gastroenterol, Utrecht, Netherlands
关键词
D O I
10.1046/j.1365-2036.2000.014s2019.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The interplay between contraction and relaxation in the gall-bladder muscularis leads to appropriate gall-bladder emptying and refilling during fasting and in the postprandial state in vivo. Several studies in both human and animal models have focused on cellular and molecular events in the gall-bladder wall in health and disease in vitro. Principal methods to study gallbladder smooth muscle function include receptor binding studies (at the level of plasmamembranes or histological sections), phase contrast microscopy (at the level of isolated smooth muscle cells), and tensiometry (at the level of smooth muscle strips or the whole gallbladder). At a very early stage, cholesterol gallstone disease is characterized by exposure of the gall-bladder wall to excess of biliary cholesterol and the cytotoxic effect of the bile salt deoxycholate. On a long-term basis, a form of gall-bladder leiomyopathy develops with defects involving the mechanisms of signal transduction at the level of plasmamembranes. The end-stage result is pathological contraction and/or relaxation of smooth musculature, impaired gall-bladder motility and gallbladder stasis, all key factors in the pathogenesis of biliary cholesterol crystallization and gallstones.
引用
收藏
页码:19 / 26
页数:8
相关论文
共 84 条
[1]   RADIOGRAPHIC EVIDENCE OF CHOLECYSTOKININ OCTAPEPTIDE RECEPTORS IN THE HAMSTER GALLBLADDER [J].
AOKI, T ;
UENO, T ;
TOYONAGA, A ;
SAKATA, R ;
KIMURA, Y ;
GONDO, K ;
INUZUKA, S ;
TORIMURA, T ;
YOSHIDA, H ;
SASAKI, E ;
TANIKAWA, K .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1991, 26 (11) :1165-1172
[2]   Pathogenesis of cholesterol gallstones: A parsimonious hypothesis [J].
Apstein, MD ;
Carey, MC .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1996, 26 (05) :343-352
[3]   GALLBLADDER CONTRACTION IN PATIENTS WITH PIGMENT AND CHOLESTEROL STONES [J].
BEHAR, J ;
LEE, KY ;
THOMPSON, WR ;
BIANCANI, P .
GASTROENTEROLOGY, 1989, 97 (06) :1479-1484
[4]   PHARMACOLOGICAL CHARACTERIZATION OF EXCITATORY AND INHIBITORY CHOLECYSTOKININ RECEPTORS OF THE CAT GALLBLADDER AND SPHINCTER OF ODDI [J].
BEHAR, J ;
BIANCANI, P .
GASTROENTEROLOGY, 1987, 92 (03) :764-770
[5]   INOSITOL TRISPHOSPHATE RESTORES IMPAIRED HUMAN GALLBLADDER MOTILITY ASSOCIATED WITH CHOLESTEROL STONES [J].
BEHAR, J ;
RHIM, BY ;
THOMPSON, W ;
BIANCANI, P .
GASTROENTEROLOGY, 1993, 104 (02) :563-568
[6]   In vitro contractility of stimulated and non-stimulated human gallbladder muscle [J].
Bird, NC ;
Wegstapel, H ;
ChessWilliams, R ;
Johnson, AG .
NEUROGASTROENTEROLOGY AND MOTILITY, 1996, 8 (01) :63-68
[7]  
BITAR KN, 1986, J BIOL CHEM, V261, P6591
[8]  
CAREY MC, 1989, FALK SYMP, V52, P259
[9]  
CAREY MC, 1996, BILE ACIDS CHOLESTAS, P147
[10]  
CHEN Q, 1995, J PHARMACOL EXP THER, V273, P650