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1
Highlight report: New insights in liver physiology: Canalicular bile flux is diffusion dominated.重点报告:肝脏生理学的新见解:胆小管胆汁流量以扩散为主。
EXCLI J. 2020 Aug 31;19:1208-1210. doi: 10.17179/excli2020-2836. eCollection 2020.
2
Molecular alterations of canalicular transport systems in experimental models of cholestasis: possible functional correlations.胆汁淤积实验模型中小管转运系统的分子改变:可能的功能相关性。
Yale J Biol Med. 1997 Jul-Aug;70(4):365-78.
3
Sulindac is excreted into bile by a canalicular bile salt pump and undergoes a cholehepatic circulation in rats.舒林酸通过胆小管胆盐泵排泄到胆汁中,并在大鼠体内进行肝肠循环。
Gastroenterology. 1999 Oct;117(4):962-71. doi: 10.1016/s0016-5085(99)70356-2.
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Molecular mechanisms of hepatic bile salt transport from sinusoidal blood into bile.肝脏中胆汁盐从窦状隙血液转运至胆汁的分子机制。
Am J Physiol. 1995 Dec;269(6 Pt 1):G801-12. doi: 10.1152/ajpgi.1995.269.6.G801.
5
Canalicular bile salt-independent bile formation: concepts and clues from electrolyte transport in rat liver.胆小管非胆盐依赖性胆汁生成:来自大鼠肝脏电解质转运的概念与线索
Am J Physiol. 1983 Mar;244(3):G233-46. doi: 10.1152/ajpgi.1983.244.3.G233.
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[Anatomy and physiology of the liver secretory apparatus].[肝脏分泌器官的解剖学与生理学]
Arq Gastroenterol. 1980 Jul-Sep;17(3):149-60.
7
Hepatic bile formation: bile acid transport and water flow into the canalicular conduit.肝胆汁形成:胆汁酸转运和水流入胆小管。
Am J Physiol Gastrointest Liver Physiol. 2020 Nov 1;319(5):G609-G618. doi: 10.1152/ajpgi.00078.2020. Epub 2020 Sep 16.
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Proteomic Analysis of the Rat Canalicular Membrane Reveals Expression of a Complex System of P4-ATPases in Liver.大鼠胆小管膜的蛋白质组学分析揭示了肝脏中P4-ATP酶复杂系统的表达。
PLoS One. 2016 Jun 27;11(6):e0158033. doi: 10.1371/journal.pone.0158033. eCollection 2016.
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Adaptive changes in hepatobiliary transporter expression in primary biliary cirrhosis.原发性胆汁性肝硬化中肝胆转运体表达的适应性变化。
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The rat liver ecto-ATPase is also a canalicular bile acid transport protein.大鼠肝脏外切ATP酶也是一种胆小管胆汁酸转运蛋白。
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本文引用的文献

1
Intravital Dynamic and Correlative Imaging of Mouse Livers Reveals Diffusion-Dominated Canalicular and Flow-Augmented Ductular Bile Flux.活体动态及相关成像技术揭示了小鼠肝脏中以扩散为主导的胆小管和血流增强的胆小管胆汁流。
Hepatology. 2021 Apr;73(4):1531-1550. doi: 10.1002/hep.31422. Epub 2021 Mar 16.
2
Pipe-3D: A Pipeline Based on Immunofluorescence, 3D Confocal Imaging, Reconstructions, and Morphometry for Biliary Network Analysis in Cholestasis.Pipe-3D:一种基于免疫荧光、三维共聚焦成像、重建和形态测量学的管道,用于胆汁淤积中胆管网络分析。
Methods Mol Biol. 2019;1981:25-53. doi: 10.1007/978-1-4939-9420-5_3.
3
Cellular Clearance and Biological Activity of Calciprotein Particles Depend on Their Maturation State and Crystallinity.钙磷蛋白颗粒的细胞清除率和生物学活性取决于其成熟状态和结晶度。
Front Immunol. 2018 Sep 4;9:1991. doi: 10.3389/fimmu.2018.01991. eCollection 2018.
4
Bile Microinfarcts in Cholestasis Are Initiated by Rupture of the Apical Hepatocyte Membrane and Cause Shunting of Bile to Sinusoidal Blood.胆汁微梗死在胆汁淤积中是由肝细胞顶膜破裂引发的,并导致胆汁分流到窦状隙血液。
Hepatology. 2019 Feb;69(2):666-683. doi: 10.1002/hep.30213. Epub 2018 Nov 19.
5
Physiologically-based modelling in mice suggests an aggravated loss of clearance capacity after toxic liver damage.基于生理学的小鼠模型研究表明,在肝毒性损伤后,清除能力的损失加剧。
Sci Rep. 2017 Jul 24;7(1):6224. doi: 10.1038/s41598-017-04574-z.
6
In vivo imaging of systemic transport and elimination of xenobiotics and endogenous molecules in mice.小鼠体内异生物素和内源性分子的全身转运与消除的活体成像
Arch Toxicol. 2017 Mar;91(3):1335-1352. doi: 10.1007/s00204-016-1906-5. Epub 2016 Dec 20.
7
The ascending pathophysiology of cholestatic liver disease.胆汁淤积性肝病的上行发病机制。
Hepatology. 2017 Feb;65(2):722-738. doi: 10.1002/hep.28965.
8
Model-guided identification of a therapeutic strategy to reduce hyperammonemia in liver diseases.基于模型指导的治疗策略鉴定,以降低肝脏疾病中的血氨过多症。
J Hepatol. 2016 Apr;64(4):860-71. doi: 10.1016/j.jhep.2015.11.018. Epub 2015 Nov 27.
9
Cholestasis-induced adaptive remodeling of interlobular bile ducts.胆汁淤积诱导的小叶间胆管适应性重塑。
Hepatology. 2016 Mar;63(3):951-64. doi: 10.1002/hep.28373. Epub 2016 Jan 14.
10
Optimality in the zonation of ammonia detoxification in rodent liver.啮齿动物肝脏中氨解毒分区的最优性
Arch Toxicol. 2015 Nov;89(11):2069-78. doi: 10.1007/s00204-015-1596-4. Epub 2015 Oct 5.

重点报告:肝脏生理学的新见解:胆小管胆汁流量以扩散为主。

Highlight report: New insights in liver physiology: Canalicular bile flux is diffusion dominated.

作者信息

Ezzat Ahmed Ahmed

机构信息

Department of Biology, College of Science, King Khalid University, 61413 Abha, Asir, Saudi Arabia.

出版信息

EXCLI J. 2020 Aug 31;19:1208-1210. doi: 10.17179/excli2020-2836. eCollection 2020.

DOI:10.17179/excli2020-2836
PMID:33013271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7527507/
Abstract

One of the central functions of the liver is excretion of bile into the intestine. Currently, bile excretion is explained by the osmotic model, according to which bile acids are excreted by hepatocytes into the bile canaliculi and since bile acids are osmotically active they draw water into the canalicular lumen. Bile canaliculi are closed at the central side. Therefore, bile was postulated to flow to the open side into the ducts. However, bile flow in canaliculi has never been measured because of the small canalicular diameter which does not allow analysis of flux by conventional methods. Recently, methods have been developed that allow flow analysis in bile canaliculi and ducts. Interestingly, no measurable directed flow was observed in the canaliculi. Instead, small molecules in bile canaliculi reached the larger bile ducts by diffusion. Only there measurable flow sets in. The pathophysiological implications of this novel observation are discussed.

摘要

肝脏的核心功能之一是将胆汁排泄到肠道。目前,胆汁排泄是通过渗透模型来解释的,根据该模型,肝细胞将胆汁酸排泄到胆小管中,由于胆汁酸具有渗透活性,它们会将水吸入胆小管腔。胆小管在中央侧是封闭的。因此,推测胆汁会流向开放侧进入胆管。然而,由于胆小管直径太小,无法用传统方法分析通量,所以从未测量过胆小管内的胆汁流动。最近,已经开发出了能够分析胆小管和胆管内流动的方法。有趣的是,在胆小管中未观察到可测量的定向流动。相反,胆小管中的小分子通过扩散进入较大的胆管。只有在胆管中才会出现可测量的流动。本文讨论了这一新发现的病理生理学意义。