Carulli N, Loria P, Bertolotti M, Ponz de Leon M, Menozzi D, Medici G, Piccagli I
J Clin Invest. 1984 Aug;74(2):614-24. doi: 10.1172/JCI111459.
To elucidate the mechanism responsible for the bile acid-induced changes of biliary lipid secretion, we evaluated bile flow and biliary output of bile acids, cholesterol, phospholipids, and alkaline phosphatase activity in seven cholecystectomized subjects with a balloon occludable T-tube during two experimental periods: (a) depletion of the endogenous bile acid pool and (b) replacement of the pool by means of duodenal infusion with individual bile acids, such as deoxycholic (DCA), chenodeoxycholic (CDCA), cholic (CA), and ursodeoxycholic (UDCA) acids. Bile flow, cholesterol, and phospholipid output were linearly related to bile acid secretion in all experimental periods. During the replacement periods, the amount of cholesterol and phospholipids coupled to bile acids was significantly different (at 1% level at least) for each individual bile acid secreted; it was the highest during DCA secretion (slope value: 0.209 for cholesterol and 0.434 for phospholipids) followed, in the order, by CDCA (0.078 and 1.794), CA (0.044 and 0.127), and UDCA (0.030 and 0.122). The phospholipid to cholesterol ratio was higher during secretion of CA and UDCA as compared with DCA and CDCA. The secretion of CA seemed to stimulate a greater bile flow than the other bile acids did. The infusion of all bile acids, except UDCA, induced an increase of biliary alkaline phosphatase activity as compared with the values of the depletion period. The mean highest increase (13-fold the pretreatment value) was observed during DCA secretion followed by CDCA (fivefold) and CA (1.5-fold). These results would suggest that the physical chemical properties, namely the lipid-solubilizing capacity, of bile acids could directly contribute to the regulation of biliary lipid secretion. The observed changes in biliary alkaline phosphatase activity lend support to the view that bile acid-induced lipid secretion may be, at least in part, contributed by membrane solubilization.
为阐明胆汁酸引起胆汁脂质分泌变化的机制,我们在两个实验阶段,对7例胆囊切除且带有可球囊阻塞T管的受试者的胆汁流量、胆汁酸、胆固醇、磷脂的胆汁排出量及碱性磷酸酶活性进行了评估:(a) 内源性胆汁酸池耗竭期;(b) 通过十二指肠输注个别胆汁酸(如脱氧胆酸(DCA)、鹅脱氧胆酸(CDCA)、胆酸(CA)和熊去氧胆酸(UDCA))来补充胆汁酸池期。在所有实验阶段,胆汁流量、胆固醇和磷脂排出量均与胆汁酸分泌呈线性相关。在补充期,每种分泌的个别胆汁酸与胆汁酸结合的胆固醇和磷脂量有显著差异(至少在1%水平);在DCA分泌期间最高(胆固醇的斜率值为0.209,磷脂为0.434),其次依次为CDCA(0.078和1.794)、CA(0.044和0.127)和UDCA(0.030和0.122)。与DCA和CDCA相比,CA和UDCA分泌期间磷脂与胆固醇的比值更高。CA的分泌似乎比其他胆汁酸刺激的胆汁流量更大。与耗竭期的值相比,除UDCA外,所有胆汁酸的输注均导致胆汁碱性磷酸酶活性增加。在DCA分泌期间观察到平均最高增幅(为预处理值的13倍),其次是CDCA(5倍)和CA(1.5倍)。这些结果表明,胆汁酸的物理化学性质,即脂质溶解能力,可能直接参与胆汁脂质分泌的调节。胆汁碱性磷酸酶活性的观察变化支持了这样一种观点,即胆汁酸诱导的脂质分泌可能至少部分是由膜溶解作用所致。