Housset Chantal, Chrétien Yues, Debray Dominique, Chignard Nicolas
Sorbonne Universités, UPMC Univ Paris 06, INSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition (ICAN), Paris, France.
Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Antoine, Centre de Référence Maladies Rares (CMR) des Maladies Inflammatoires des Voies Biliaires (MIVB), Service d'Hépatologie, Paris, France.
Compr Physiol. 2016 Jun 13;6(3):1549-77. doi: 10.1002/cphy.c150050.
The gallbladder stores and concentrates bile between meals. Gallbladder motor function is regulated by bile acids via the membrane bile acid receptor, TGR5, and by neurohormonal signals linked to digestion, for example, cholecystokinin and FGF15/19 intestinal hormones, which trigger gallbladder emptying and refilling, respectively. The cycle of gallbladder filling and emptying controls the flow of bile into the intestine and thereby the enterohepatic circulation of bile acids. The gallbladder also largely contributes to the regulation of bile composition by unique absorptive and secretory capacities. The gallbladder epithelium secretes bicarbonate and mucins, which both provide cytoprotection against bile acids. The reversal of fluid transport from absorption to secretion occurs together with bicarbonate secretion after feeding, predominantly in response to an adenosine 3',5'-cyclic monophosphate (cAMP)-dependent pathway triggered by neurohormonal factors, such as vasoactive intestinal peptide. Mucin secretion in the gallbladder is stimulated predominantly by calcium-dependent pathways that are activated by ATP present in bile, and bile acids. The gallbladder epithelium has the capacity to absorb cholesterol and provides a cholecystohepatic shunt pathway for bile acids. Changes in gallbladder motor function not only can contribute to gallstone disease, but also subserve protective functions in multiple pathological settings through the sequestration of bile acids and changes in the bile acid composition. Cholecystectomy increases the enterohepatic recirculation rates of bile acids leading to metabolic effects and an increased risk of nonalcoholic fatty liver disease, cirrhosis, and small-intestine carcinoid, independently of cholelithiasis. Among subjects with gallstones, cholecystectomy remains a priority in those at risk of gallbladder cancer, while others could benefit from gallbladder-preserving strategies. © 2016 American Physiological Society. Compr Physiol 6:1549-1577, 2016.
胆囊在两餐之间储存和浓缩胆汁。胆囊运动功能受胆汁酸通过膜胆汁酸受体TGR5调节,也受与消化相关的神经激素信号调节,例如胆囊收缩素和FGF15/19肠道激素,它们分别触发胆囊排空和重新充盈。胆囊充盈和排空的循环控制胆汁流入肠道,从而控制胆汁酸的肠肝循环。胆囊还通过独特的吸收和分泌能力在很大程度上有助于胆汁成分的调节。胆囊上皮分泌碳酸氢盐和粘蛋白,两者都提供针对胆汁酸的细胞保护。进食后,液体运输从吸收转变为分泌,这与碳酸氢盐分泌同时发生,主要是响应由神经激素因子(如血管活性肠肽)触发的3',5'-环磷酸腺苷(cAMP)依赖性途径。胆囊中粘蛋白的分泌主要由胆汁中存在的ATP和胆汁酸激活的钙依赖性途径刺激。胆囊上皮具有吸收胆固醇的能力,并为胆汁酸提供一条胆囊肝分流途径。胆囊运动功能的改变不仅可导致胆结石疾病,还可通过胆汁酸的隔离和胆汁酸组成的变化在多种病理情况下发挥保护作用。胆囊切除术会增加胆汁酸的肠肝循环率,导致代谢效应以及非酒精性脂肪性肝病、肝硬化和小肠类癌风险增加,这与胆结石无关。在患有胆结石的受试者中,胆囊切除术对于有胆囊癌风险的人仍然是优先选择,而其他人可能从保留胆囊的策略中受益。©2016美国生理学会。综合生理学6:1549 - 1577, 2016。