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本文引用的文献

1
Imaging of blood flow using hyperpolarized [(13)C]urea in preclinical cancer models.使用超极化 [(13)C] 尿素在临床前癌症模型中进行血流成像。
J Magn Reson Imaging. 2011 Mar;33(3):692-7. doi: 10.1002/jmri.22484.
2
Analysis of cancer metabolism by imaging hyperpolarized nuclei: prospects for translation to clinical research.通过成像技术分析癌症代谢:向临床研究转化的前景。
Neoplasia. 2011 Feb;13(2):81-97. doi: 10.1593/neo.101102.
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Synthesis and in vivo evaluation of p-18F-Fluorohippurate as a new radiopharmaceutical for assessment of renal function by PET.合成并体内评价 p-18F-氟 hippurate 作为一种新的放射性药物,用于通过 PET 评估肾功能。
J Nucl Med. 2011 Jan;52(1):147-53. doi: 10.2967/jnumed.110.075895. Epub 2010 Dec 13.
4
Expression of transporters involved in urine concentration recovers differently after cessation of lithium treatment.表达转运体参与尿液浓缩的恢复在锂治疗停止后不同。
Am J Physiol Renal Physiol. 2010 Mar;298(3):F601-8. doi: 10.1152/ajprenal.00424.2009. Epub 2009 Dec 23.
5
The physiology of urinary concentration: an update.尿浓缩生理:最新进展。
Semin Nephrol. 2009 May;29(3):178-95. doi: 10.1016/j.semnephrol.2009.03.008.
6
Contrast-Induced Nephropathy (CIN) Consensus Working Panel: executive summary.造影剂诱导的肾病(CIN)共识工作小组:执行摘要。
Rev Cardiovasc Med. 2006 Fall;7(4):177-97.
7
Gadolinium-based MR contrast agents and nephrogenic systemic fibrosis.钆基磁共振造影剂与肾源性系统性纤维化
Radiology. 2007 Mar;242(3):647-9. doi: 10.1148/radiol.2423061640. Epub 2007 Jan 9.
8
Urearetics: a small molecule screen yields nanomolar potency inhibitors of urea transporter UT-B.尿素利尿药:小分子筛选产生尿素转运蛋白UT-B的纳摩尔效力抑制剂。
FASEB J. 2007 Feb;21(2):551-63. doi: 10.1096/fj.06-6979com. Epub 2007 Jan 3.
9
Vasopressin increases plasma membrane accumulation of urea transporter UT-A1 in rat inner medullary collecting ducts.血管加压素可增加大鼠肾内髓集合管中尿素转运体UT-A1在质膜的积聚。
J Am Soc Nephrol. 2006 Oct;17(10):2680-6. doi: 10.1681/ASN.2006030246. Epub 2006 Sep 7.
10
Real-time metabolic imaging.实时代谢成像
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利用 ¹³C 磁共振成像技术在体监测大鼠肾脏中尿素的转运。

Monitoring urea transport in rat kidney in vivo using hyperpolarized ¹³C magnetic resonance imaging.

机构信息

Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.

出版信息

Am J Physiol Renal Physiol. 2012 Jun 15;302(12):F1658-62. doi: 10.1152/ajprenal.00640.2011. Epub 2012 Apr 4.

DOI:10.1152/ajprenal.00640.2011
PMID:22492940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3378100/
Abstract

Urea functions as a key osmolyte in the urinary concentrating mechanism of the inner medulla. The urea transporter UT-A1 is upregulated by antidiuretic hormone, facilitating faster equilibration of urea between the lumen and interstitium of the inner medullary collecting duct, resulting in the formation of more highly concentrated urine. New methods in dynamic nuclear polarization, providing ∼50,000-fold enhancement of nuclear magnetic resonance signals in the liquid state, offer a novel means to monitor this process in vivo using magnetic resonance imaging. In this study, we detected significant signal differences in the rat kidney between acute diuretic and antidiuretic states, using dynamic (13)C magnetic resonance imaging following a bolus infusion of hyperpolarized [(13)C]urea. More rapid medullary enhancement was observed under antidiuresis, consistent with known upregulation of UT-A1.

摘要

尿素在内髓尿液浓缩机制中作为一种关键渗透物发挥作用。抗利尿激素上调尿素转运蛋白 UT-A1,促进尿素在髓袢升支粗段收集管的管腔和间质之间更快地达到平衡,从而形成更高浓度的尿液。动态核极化的新方法提供了约 50,000 倍的液体状态下磁共振信号增强,为使用磁共振成像在体内监测该过程提供了一种新方法。在这项研究中,我们使用超极化 [(13)C]尿素的单次推注后进行动态 (13)C 磁共振成像,在急性利尿和抗利尿状态下检测到大鼠肾脏中的显著信号差异。在抗利尿状态下观察到更快的髓质增强,这与 UT-A1 的已知上调一致。