• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

钆塞酸二钠和钆喷酸葡胺在Wistar大鼠肝脏和肾脏中的弛豫率

The relaxivity of Gd-EOB-DTPA and Gd-DTPA in liver and kidney of the Wistar rat.

作者信息

Shuter B, Tofts P S, Wang S C, Pope J M

机构信息

Department of Radiology, Royal North Shore Hospital, St. Leonards, NSW, Australia.

出版信息

Magn Reson Imaging. 1996;14(3):243-53. doi: 10.1016/0730-725x(95)02097-d.

DOI:10.1016/0730-725x(95)02097-d
PMID:8725190
Abstract

The NMR relaxivities of Gd-EOB-DTPA and Gd-DTPA were determined in the kidney and liver of intact male Wistar rats immediately following sacrifice and in vitro in solutions and gels, at 1.5 T using a clinical MR scanner, T1 and T2 values of tissue samples were derived from spin-echo image sequences. Tissue gadolinium concentrations were determined by radioassay of Gd153, Gd-EOB-DTPA T1 and T2 relaxivities, R1 and R2 (s-1 mmole-1 kg), were found to be 10.7 +/- 0.5 and 22.5 +/- 3.2 respectively, for liver, 2.4 +/- 0.2 and 12.1 +/- 1.7 for kidney cortex, 2.7 +/- 0.2 and 14.5 +/- 1.9 for kidney outer medulla, 2.0 +/- 0.2 and 11.4 +/- 2.1 for kidney inner medulla. Gd-DTPA R1 and R2 were found to be 4.8 +/- 0.4 and 14.5 +/- 3.7 for liver, 1.2 +/- 0.1 and 7.9 +/- 0.8 for kidney cortex, 1.6 +/- 0.1 and 10.2 +/- 1.4 for kidney outer medulla, 1.3 +/- 0.1 and 10.2 +/- 1.2 for kidney inner medulla. Gd-EOB-DTPA and Gd-DTPA R1 was increased in liver compared to agarose gets at 38 degrees C (4.49 +/- 0.03 and 3.47 +/- 0.06), but reduced in kidney tissues. All R2 were elevated compared to agarose gels at 38 degrees C (5.72 +/- 0.12 and 4.12 +/- 0.03). Elevated R2 and R1 (expressed in terms of the concentration of gadolinium per kg of tissue) can be accounted for in part by the lower water content of tissues compared with gels or solutions increased microviscosity and binding to macromolecules. In addition, susceptibility effects may give rise to further increases in R2. By contrast, the reduced R1 observed in kidney may be the result of compartmentalization of the magnetopharmaceuticals. Statistically improved fits were obtained for T1 recovery curves for liver in the presence of Gd-EOB-DTPA when a dual exponential model was used. Assuming in vitro values for the relaxivities of these artificial contrast agents will lead to inaccuracies when relating observed signal enhancement factors to tissue gadolinium concentration.

摘要

在处死雄性Wistar大鼠后,立即在其肾脏和肝脏中,以及在体外溶液和凝胶中,使用临床磁共振扫描仪在1.5T场强下测定钆塞酸二钠(Gd-EOB-DTPA)和钆喷酸葡胺(Gd-DTPA)的核磁共振弛豫率。组织样本的T1和T2值由自旋回波图像序列得出。通过对Gd153进行放射性测定来确定组织中的钆浓度。发现Gd-EOB-DTPA在肝脏中的T1和T2弛豫率R1和R2(s-1 mmol-1 kg)分别为10.7±0.5和22.5±3.2,肾皮质中为2.4±0.2和12.1±1.7,肾外髓质中为2.7±0.2和14.5±1.9,肾内髓质中为2.0±0.2和11.4±2.1。发现Gd-DTPA在肝脏中的R1和R2分别为4.8±0.4和14.5±3.7,肾皮质中为1.2±0.1和7.9±0.8,肾外髓质中为1.6±0.1和10.2±1.4,肾内髓质中为1.3±0.1和10.2±1.2。与38℃的琼脂糖凝胶相比,Gd-EOB-DTPA和Gd-DTPA在肝脏中的R1升高(分别为4.49±0.03和3.47±0.06),但在肾脏组织中降低。与38℃的琼脂糖凝胶相比,所有的R2均升高(分别为5.72±0.12和4.12±0.03)。R2和R1升高(以每千克组织中钆的浓度表示)部分可归因于与凝胶或溶液相比,组织中的水含量较低、微粘度增加以及与大分子的结合。此外,磁化率效应可能导致R2进一步升高。相比之下,在肾脏中观察到的R1降低可能是磁性药物分隔的结果。当使用双指数模型时,在存在Gd-EOB-DTPA的情况下,肝脏的T1恢复曲线在统计学上拟合得更好。假设这些人工造影剂的弛豫率为体外值,在将观察到的信号增强因子与组织钆浓度相关联时会导致不准确。

相似文献

1
The relaxivity of Gd-EOB-DTPA and Gd-DTPA in liver and kidney of the Wistar rat.钆塞酸二钠和钆喷酸葡胺在Wistar大鼠肝脏和肾脏中的弛豫率
Magn Reson Imaging. 1996;14(3):243-53. doi: 10.1016/0730-725x(95)02097-d.
2
Relaxivity of Gd-EOB-DTPA in the normal and biliary obstructed guinea pig.钆塞酸二钠在正常及胆道梗阻豚鼠体内的弛豫率
J Magn Reson Imaging. 1998 Jul-Aug;8(4):853-61. doi: 10.1002/jmri.1880080415.
3
Gadolinium-ethoxybenzyl-DTPA, a new liver-specific magnetic resonance contrast agent. Kinetic and enhancement patterns in normal and cholestatic rats.钆-乙氧基苄基-二乙三胺五乙酸,一种新型肝脏特异性磁共振造影剂。正常及胆汁淤积大鼠的动力学和增强模式。
Invest Radiol. 1992 Aug;27(8):612-9.
4
Hepatic kinetics and magnetic resonance imaging of gadolinium-EOB-DTPA in dogs.钆塞酸二钠在犬体内的肝脏动力学及磁共振成像
Invest Radiol. 1996 Apr;31(4):211-7. doi: 10.1097/00004424-199604000-00005.
5
Ytterbium- and dysprosium-EOB-DTPA. A new prototype of liver-specific contrast agents for computed tomography.镱与镝标记的乙氧基苄基二乙烯三胺五乙酸。一种用于计算机断层扫描的新型肝脏特异性造影剂原型。
Invest Radiol. 1996 Aug;31(8):502-11. doi: 10.1097/00004424-199608000-00006.
6
Ni-DTPA doped agarose gel--a phantom material for Gd-DTPA enhancement measurements.镍-二乙三胺五乙酸掺杂琼脂糖凝胶——一种用于钆-二乙三胺五乙酸增强测量的体模材料。
Magn Reson Imaging. 1993;11(1):125-33. doi: 10.1016/0730-725x(93)90420-i.
7
Hepatic kinetics and magnetic resonance imaging of gadolinium ethoxybenzyl diethylenetriaminepentacetic acid (Gd-EOB-DTPA) in dogs.钆乙氧基苄基二乙三胺五乙酸(Gd-EOB-DTPA)在犬体内的肝脏动力学及磁共振成像
Australas Radiol. 1993 Aug;37(3):252-5. doi: 10.1111/j.1440-1673.1993.tb00067.x.
8
Multinuclear MR characterization of a new hepatobiliary contrast agent. Preliminary results.一种新型肝胆造影剂的多核磁共振特征:初步结果
Acta Radiol Suppl. 1997;412:135-8.
9
Elimination of gadolinium-ethoxybenzyl-DTPA in a rat model of severely impaired liver and kidney excretory function. An experimental study in rats.严重肝肾排泄功能受损大鼠模型中钆乙氧基苄基二乙三胺五乙酸的清除。大鼠实验研究。
Invest Radiol. 1994 Feb;29(2):213-6. doi: 10.1097/00004424-199402000-00017.
10
Pharmacokinetics in rats, dogs and monkeys of a gadolinium chelate used as a liver-specific contrast agent for magnetic resonance imaging.一种用作肝脏特异性磁共振成像造影剂的钆螯合物在大鼠、狗和猴子体内的药代动力学。
Arzneimittelforschung. 1993 Aug;43(8):927-31.

引用本文的文献

1
Hepatic MR imaging using IDEAL-IQ sequence: Will Gd-EOB-DTPA interfere with reproductivity of fat fraction quantification?使用IDEAL-IQ序列的肝脏磁共振成像:钆塞酸二钠会干扰脂肪分数定量的重复性吗?
World J Clin Cases. 2023 Sep 6;11(25):5887-5896. doi: 10.12998/wjcc.v11.i25.5887.
2
Assessment of hepatic function employing hepatocyte specific contrast agent concentrations to multifactorially evaluate fibrotic remodeling.利用肝细胞特异性造影剂浓度评估肝功能以多因素评估纤维化重塑。
Quant Imaging Med Surg. 2023 Jul 1;13(7):4284-4294. doi: 10.21037/qims-22-884. Epub 2023 May 4.
3
Mathematical models for biomarker calculation of drug-induced liver injury in humans and experimental models based on gadoxetate enhanced magnetic resonance imaging.
基于钆塞酸增强磁共振成像的人源性药物性肝损伤生物标志物计算的数学模型及实验模型。
PLoS One. 2023 Jan 6;18(1):e0279168. doi: 10.1371/journal.pone.0279168. eCollection 2023.
4
Ex vivo gadoxetate relaxivities in rat liver tissue and blood at five magnetic field strengths from 1.41 to 7 T.在 1.41 至 7T 的五个磁场强度下,大鼠肝组织和血液中的体外钆塞酸弛豫率。
NMR Biomed. 2021 Jan;34(1):e4401. doi: 10.1002/nbm.4401. Epub 2020 Aug 26.
5
Model-inferred mechanisms of liver function from magnetic resonance imaging data: Validation and variation across a clinically relevant cohort.从磁共振成像数据推断肝功能的模型:在具有临床相关性的队列中的验证和变化。
PLoS Comput Biol. 2019 Jun 25;15(6):e1007157. doi: 10.1371/journal.pcbi.1007157. eCollection 2019 Jun.
6
Effect of gadolinium on hepatic fat quantification using multi-echo reconstruction technique with T2* correction and estimation.钆对采用T2*校正与估计的多回波重建技术进行肝脏脂肪定量的影响。
Eur Radiol. 2016 Jun;26(6):1913-20. doi: 10.1007/s00330-015-3981-z. Epub 2015 Sep 17.
7
Physiologically realistic and validated mathematical liver model reveals [corrected] hepatobiliary transfer rates for Gd-EOB-DTPA using human DCE-MRI data.生理逼真且经过验证的数学肝脏模型利用人体动态对比增强磁共振成像(DCE-MRI)数据揭示了钆塞酸二钠(Gd-EOB-DTPA)的肝胆转运速率[已修正]。
PLoS One. 2014 Apr 18;9(4):e95700. doi: 10.1371/journal.pone.0095700. eCollection 2014.
8
Functional MRI of the kidneys.肾脏功能磁共振成像。
J Magn Reson Imaging. 2013 Feb;37(2):282-93. doi: 10.1002/jmri.23717.
9
Precise measurement of renal filtration and vascular parameters using a two-compartment model for dynamic contrast-enhanced MRI of the kidney gives realistic normal values.使用双室模型对肾脏动态对比增强 MRI 进行精确测量,可以得到真实的正常肾滤过率和血管参数值。
Eur Radiol. 2012 Jun;22(6):1320-30. doi: 10.1007/s00330-012-2382-9. Epub 2012 Mar 14.
10
Consensus report of the 4th International Forum for Gadolinium-Ethoxybenzyl-Diethylenetriamine Pentaacetic Acid Magnetic Resonance Imaging.第四届钆乙氧基苯二乙酸二乙烯三胺五乙酸磁共振成像国际论坛共识报告。
Korean J Radiol. 2011 Jul-Aug;12(4):403-15. doi: 10.3348/kjr.2011.12.4.403. Epub 2011 Jul 22.