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Zonation of hepatic bile salt transporters.

作者信息

Baier P K, Hempel S, Waldvogel B, Baumgartner U

机构信息

Department of Surgery, University of Freiburg, Freiburg, Germany.

出版信息

Dig Dis Sci. 2006 Mar;51(3):587-93. doi: 10.1007/s10620-006-3174-3.

DOI:10.1007/s10620-006-3174-3
PMID:16614971
Abstract

Pericentral and periportal hepatocytes differ in their capacity to eliminate and velocity of eliminating bile acids and other organic anions. We wonder whether differences in the distribution of anion transporters (ntcp [M77479], besp [NM_031760], mrp2 [NM_012833], oatp1 [NM_017111], oatp2 [NM_131906]) cause the differences in bile acid excretion. Therefore, we analyzed the distribution of these anion transporters in periportal and pericentral cells by immunohistology, their mRNA by quantitative PCR, and regulating nuclear factors (NF-kappaB, HNF1, HNF3, HNF4, FXR, PXR) by gel shift assay. We did not find any differences in nuclear factors or regarding the proteins that could explain the zonal differences in anion transport.

摘要

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本文引用的文献

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Role of farnesoid X receptor in determining hepatic ABC transporter expression and liver injury in bile duct-ligated mice.法尼酯X受体在胆管结扎小鼠肝脏ABC转运蛋白表达及肝损伤决定中的作用
Gastroenterology. 2003 Sep;125(3):825-38. doi: 10.1016/s0016-5085(03)01068-0.
2
The 3alpha-hydroxy-steroid-dehydrogenase-mRNA and -protein are more prevalent in pericentral than in periportal hepatocytes.3α-羟基类固醇脱氢酶的信使核糖核酸和蛋白质在中央静脉周围的肝细胞中比在汇管区周围的肝细胞中更普遍。
Eur J Gastroenterol Hepatol. 2003 May;15(5):509-13. doi: 10.1097/01.meg.0000059117.41030.72.
3
Bile salt transporters: molecular characterization, function, and regulation.
胆盐转运体:分子特征、功能及调控
Physiol Rev. 2003 Apr;83(2):633-71. doi: 10.1152/physrev.00027.2002.
4
Bile acid regulation of hepatic physiology: I. Hepatocyte transport of bile acids.胆汁酸对肝脏生理的调节:I. 肝细胞对胆汁酸的转运
Am J Physiol Gastrointest Liver Physiol. 2003 Feb;284(2):G175-9. doi: 10.1152/ajpgi.00409.2002.
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Identification of bile acid precursors as endogenous ligands for the nuclear xenobiotic pregnane X receptor.鉴定胆汁酸前体作为核外源性孕烷X受体的内源性配体。
Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):223-8. doi: 10.1073/pnas.0237082100. Epub 2002 Dec 30.
6
Effects of bile salt flux variations on the expression of hepatic bile salt transporters in vivo in mice.胆汁盐通量变化对小鼠体内肝脏胆汁盐转运蛋白表达的影响。
J Hepatol. 2002 Nov;37(5):556-63. doi: 10.1016/s0168-8278(02)00247-7.
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Bile acids regulate the ontogenic expression of ileal bile acid binding protein in the rat via the farnesoid X receptor.胆汁酸通过法尼酯X受体调节大鼠回肠胆汁酸结合蛋白的个体发生表达。
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Mol Pharmacol. 2002 Apr;61(4):832-9. doi: 10.1124/mol.61.4.832.
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