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Biomed Opt Express. 2016 Aug 19;7(9):3574-3584. doi: 10.1364/BOE.7.003574. eCollection 2016 Sep 1.
2
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本文引用的文献

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The evolution of the OATP hepatic uptake transport protein family in DMPK sciences: from obscure liver transporters to key determinants of hepatobiliary clearance.DMPK科学领域中有机阴离子转运多肽(OATP)肝脏摄取转运蛋白家族的演变:从鲜为人知的肝脏转运体到肝胆清除的关键决定因素。
Xenobiotica. 2012 Jan;42(1):28-45. doi: 10.3109/00498254.2011.626464. Epub 2011 Nov 11.
2
Transcription dynamics in a physiological process: β-catenin signaling directs liver metabolic zonation.生理过程中的转录动态:β-连环蛋白信号指导肝脏代谢分区。
Int J Biochem Cell Biol. 2011 Feb;43(2):271-8. doi: 10.1016/j.biocel.2009.11.004. Epub 2009 Nov 13.
3
Hepatic glutamate metabolism: a tale of 2 hepatocytes.肝脏谷氨酸代谢:两个肝细胞的故事。
Am J Clin Nutr. 2009 Sep;90(3):857S-861S. doi: 10.3945/ajcn.2009.27462Z. Epub 2009 Jul 22.
4
In vivo dynamic metabolic imaging of obstructive cholestasis in mice.小鼠阻塞性胆汁淤积的体内动态代谢成像
Am J Physiol Gastrointest Liver Physiol. 2009 May;296(5):G1091-7. doi: 10.1152/ajpgi.90681.2008. Epub 2009 Feb 26.
5
Sex-specific extraction of organic anions by the rat liver.
Life Sci. 2008 Feb 13;82(7-8):436-43. doi: 10.1016/j.lfs.2007.12.009. Epub 2007 Dec 23.
6
Hepatocellular expression of glutamine synthetase: an indicator of morphogen actions as master regulators of zonation in adult liver.谷氨酰胺合成酶的肝细胞表达:作为成年肝脏区域化主要调节因子的形态发生素作用的指标
Prog Histochem Cytochem. 2007;41(4):201-66. doi: 10.1016/j.proghi.2006.12.001. Epub 2007 Feb 8.
7
Visualization of hepatobiliary excretory function by intravital multiphoton microscopy.通过活体多光子显微镜观察肝胆排泄功能
J Biomed Opt. 2007 Jan-Feb;12(1):014014. doi: 10.1117/1.2710237.
8
Differential regulation of sinusoidal and canalicular hepatic drug transporter expression by xenobiotics activating drug-sensing receptors in primary human hepatocytes.外源性物质激活原代人肝细胞中的药物传感受体对肝血窦和胆小管肝药物转运体表达的差异调节
Drug Metab Dispos. 2006 Oct;34(10):1756-63. doi: 10.1124/dmd.106.010033. Epub 2006 Jul 12.
9
Ultrastructural zonal heterogeneity of hepatocytes and mitochondria within the hepatic acinus during liver regeneration after partial hepatectomy.肝部分切除术后肝脏再生过程中肝腺泡内肝细胞和线粒体的超微结构区域异质性
Biol Cell. 2005 Apr;97(4):277-88. doi: 10.1042/BC20040154.
10
Mapping of the functional microcirculation in vital organs using contrast-enhanced in vivo video microscopy.使用造影增强体内视频显微镜对重要器官的功能性微循环进行映射。
Am J Physiol Heart Circ Physiol. 2005 Jan;288(1):H185-93. doi: 10.1152/ajpheart.01022.2003. Epub 2004 Sep 23.

以6 - CFDA作为模型化合物直接可视化肝胆代谢中的功能异质性。

Direct visualization of functional heterogeneity in hepatobiliary metabolism using 6-CFDA as model compound.

作者信息

Lin Chih-Ju, Li Feng-Chieh, Lee Yu-Yang, Tseng Te-Yu, Chen Wei-Liang, Hovhannisyan Vladimir, Kang Ning, Horton Nicholas G, Chiang Shu-Jen, Xu Chris, Lee Hsuan-Shu, Dong Chen-Yuan

机构信息

Department of Physics, National Taiwan University, Taipei 106, Taiwan.

School of Applied and Engineering Physics, Cornell University, Ithaca, NY, 14853, USA.

出版信息

Biomed Opt Express. 2016 Aug 19;7(9):3574-3584. doi: 10.1364/BOE.7.003574. eCollection 2016 Sep 1.

DOI:10.1364/BOE.7.003574
PMID:27699121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5030033/
Abstract

Hepatobiliary metabolism is one of the major functions of the liver. However, little is known of the relationship between the physiological location of the hepatocytes and their metabolic potential. By the combination of time-lapse multiphoton microscopy and first order kinetic constant image analysis, the hepatocellular metabolic rate of the model compound 6-carboxyfluorescein diacetate (6-CFDA) is quantified at the single cell level. We found that the mouse liver can be divided into three zones, each with distinct metabolic rate constants. The sinusoidal uptake coefficients k of Zones 1, 2, and 3 are respectively 0.239 ± 0.077, 0.295 ± 0.087, and 0.338 ± 0.133 min, the apical excreting coefficients k of Zones 1, 2, and 3 are 0.0117 ± 0.0052, 0.0175 ± 0.0052, and 0.0332 ± 0.0195 min, respectively. Our results show not only the existence of heterogeneities in hepatobiliary metabolism, but they also show that Zone 3 is the main area of metabolism.

摘要

肝胆代谢是肝脏的主要功能之一。然而,对于肝细胞的生理位置与其代谢潜能之间的关系,人们了解甚少。通过延时多光子显微镜和一级动力学常数图像分析相结合的方法,在单细胞水平上对模型化合物6-羧基荧光素二乙酸酯(6-CFDA)的肝细胞代谢率进行了量化。我们发现,小鼠肝脏可分为三个区域,每个区域具有不同的代谢速率常数。1区、2区和3区的窦状隙摄取系数k分别为0.239±0.077、0.295±0.087和0.338±0.133分钟,1区、2区和3区的顶端排泄系数k分别为0.0117±0.0052、0.0175±0.0052和0.0332±0.0195分钟。我们的研究结果不仅表明了肝胆代谢中存在异质性,还表明3区是主要的代谢区域。