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硫酸化脂质脱落至胃液中以及硫酸胆固醇与胆汁酸协同抑制胰腺DNA酶I。

Shedding of sulfated lipids into gastric fluid and inhibition of pancreatic DNase I by cholesterol sulfate in concert with bile acids.

作者信息

Iwamori M, Suzuki H, Kimura T, Iwamori Y

机构信息

Department of Biochemistry, Faculty of Science and Technology, Kinki University, Higashiosaka, Osaka, Japan.

出版信息

Biochim Biophys Acta. 2000 Sep 27;1487(2-3):268-74. doi: 10.1016/s1388-1981(00)00102-5.

Abstract

Cholesterol sulfate (CS) and sulfatides in the epithelium of the digestive tract were found in the 1000xg supernatants of digestive fluid, particularly in gastric juices containing the duodenal contents and bile acids, there being 14-131 microg of CS and 3-54 microg of sulfatides per mg of protein in the fluid, respectively. CS and sulfatides dissolved in detergents including bile acids inactivated pancreatic trypsin to the same level as by DMSO-solubilized sulfated lipids at 37 degrees C. Similarly, pancreatic DNase I was inhibited by CS solubilized with DMSO or bile acids, but not by sulfatides or other membrane lipids at 37 degrees C. Both the sulfate group and the hydrophobic side chain of CS were indispensable structures for the inhibition of DNase I. Also, the optimum molar ratio of bile acids to CS was important for expression of the inhibitory activity of CS toward DNase I, it being 0.18 of the optimum ratio for sodium taurocholate, and the molar ratio of CS to DNase I for complete inhibition was 342:1. Thus, CS was shown to play a role as an epithelial inhibitor of DNase I in concert with bile acids.

摘要

在消化液的1000xg上清液中发现了消化道上皮中的胆固醇硫酸酯(CS)和硫脂,特别是在含有十二指肠内容物和胆汁酸的胃液中,每毫克蛋白质中分别含有14 - 131微克的CS和3 - 54微克的硫脂。溶解在包括胆汁酸在内的洗涤剂中的CS和硫脂,在37℃时使胰蛋白酶失活的程度与二甲基亚砜溶解的硫酸化脂质相同。同样,胰脱氧核糖核酸酶I在37℃时被二甲基亚砜或胆汁酸溶解的CS抑制,但不被硫脂或其他膜脂抑制。CS的硫酸基团和疏水侧链都是抑制脱氧核糖核酸酶I所必需的结构。此外,胆汁酸与CS的最佳摩尔比对于CS对脱氧核糖核酸酶I的抑制活性的表达很重要,牛磺胆酸钠的最佳比例为0.18,完全抑制所需的CS与脱氧核糖核酸酶I的摩尔比为342:1。因此,CS被证明与胆汁酸协同作用,作为脱氧核糖核酸酶I的上皮抑制剂发挥作用。

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