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胆汁酸结构对仓鼠胆汁流动和胆汁脂质分泌的影响。

Influence of bile acid structure on bile flow and biliary lipid secretion in the hamster.

作者信息

Gurantz D, Hofmann A F

出版信息

Am J Physiol. 1984 Dec;247(6 Pt 1):G736-48. doi: 10.1152/ajpgi.1984.247.6.G736.

Abstract

A comprehensive study of the influence of bile acid structure on bile flow and biliary lipid secretion was carried out by infusing pure bile acids at a physiological rate into the proximal small intestine of a bile fistula hamster. Twelve individual bile acids, cholate (C), ursocholate (UC), chenodeoxycholate (CDC), and ursodeoxycholate (UDC) as their glycine (G), taurine (T), or unconjugated form, were studied so that influence of the hydroxy substituents as well as side-chain structure could be defined. The pattern of bile acid output was dependent on bile acid structure and reflected the site and rate of intestinal absorption. Conjugated bile acid output was delayed because of late ileal absorption, and TUC was poorly absorbed. Unconjugated trihydroxy bile acids, C and UC, also exhibited a delay in absorption, while CDC and UDC were absorbed immediately and achieved the highest bile acid output. Unconjugated bile acids were conjugated initially mostly with taurine and then mostly with glycine. The effect of glycine conjugates of each bile acid on bile flow and biliary lipid secretion was similar to that of their corresponding taurine conjugates. All conjugated bile acids induced a similar rate of bile flow (9-15 microliter bile/mumol bile acid), but unconjugated bile acids other than C induced more flow (20-25 microliter bile/mumol bile acid) than their corresponding conjugates. Conjugates of the dihydroxy bile acids induced a greater secretion of phospholipid and cholesterol than cholyl conjugates, whereas conjugates of UC were unique in inducing extremely low phospholipid and cholesterol secretion. For an increase of 1 mumol X min-1 X kg-1 in bile acid output, the increase in phospholipid secretion was 0.072 mumol X min X kg for GCDC and TCDC; 0.051 mumol X min-1 X kg-1 for GUDC and TUDC; and 0.030 mumol X min-1 X kg-1 for GC and TC. Increase in cholesterol output per mumol X min-1 X kg-1 of bile acid output was 0.013 mumol X min-1 X kg-1 for GCDC and TCDC, 0.011 mumol X min-1 X kg-1 for GUDC and TUDC, and 0.005 mumol X min-1 X kg-1 for GC and TC. In general, unconjugated bile acids induced more phospholipid and cholesterol than their corresponding conjugates; however, the rank-order effect of the steroid nucleus substituents was similar to that observed for the respective conjugates. These results indicate that both nuclear and side-chain structure influence the enterohepatic circulation and biliary secretory properties of bile acids.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

通过以生理速率将纯胆汁酸注入胆瘘仓鼠的近端小肠,对胆汁酸结构对胆汁流动和胆汁脂质分泌的影响进行了全面研究。研究了十二种单独的胆汁酸,即胆酸(C)、熊去氧胆酸(UC)、鹅去氧胆酸(CDC)和熊脱氧胆酸(UDC),它们分别以甘氨酸(G)、牛磺酸(T)或未结合形式存在,以便确定羟基取代基以及侧链结构的影响。胆汁酸输出模式取决于胆汁酸结构,并反映了肠道吸收的部位和速率。结合型胆汁酸输出延迟是因为回肠吸收较晚,且TUC吸收较差。未结合的三羟基胆汁酸C和UC也表现出吸收延迟,而CDC和UDC立即被吸收并实现了最高的胆汁酸输出。未结合的胆汁酸最初大多与牛磺酸结合,然后大多与甘氨酸结合。每种胆汁酸的甘氨酸结合物对胆汁流动和胆汁脂质分泌的影响与其相应的牛磺酸结合物相似。所有结合型胆汁酸诱导的胆汁流动速率相似(9 - 15微升胆汁/微摩尔胆汁酸),但除C以外的未结合胆汁酸比其相应的结合物诱导更多的胆汁流动(20 - 25微升胆汁/微摩尔胆汁酸)。二羟基胆汁酸的结合物比胆酰结合物诱导更多的磷脂和胆固醇分泌,而UC的结合物在诱导极低的磷脂和胆固醇分泌方面是独特的。对于胆汁酸输出每增加1微摩尔·分钟⁻¹·千克⁻¹,GCDC和TCDC的磷脂分泌增加量为0.072微摩尔·分钟·千克;GUDC和TUDC为0.051微摩尔·分钟⁻¹·千克⁻¹;GC和TC为0.030微摩尔·分钟⁻¹·千克⁻¹。每微摩尔·分钟⁻¹·千克⁻¹胆汁酸输出的胆固醇增加量,GCDC和TCDC为0.013微摩尔·分钟⁻¹·千克⁻¹,GUDC和TUDC为

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