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经鼓室内注射两种不同类型钆后大鼠内耳外淋巴间隙强化的多样模式:一项9.4特斯拉磁共振研究

Diverse patterns of perilymphatic space enhancement in the rat inner ear after intratympanic injection of two different types of gadolinium: a 9.4-tesla magnetic resonance study.

作者信息

Park Mina, Lee Ho Sun, Choi Jun-Jae, Kim Hyeonjin, Lee Jun Ho, Oh Seung Ha, Suh Myung-Whan

出版信息

Audiol Neurootol. 2015;20(2):112-116. doi: 10.1159/000368666. Epub 2015 Mar 4.

DOI:10.1159/000368666
PMID:25765053
Abstract

OBJECTIVE

To compare the quality of perilymphatic enhancement in the rat inner ear after intratympanic injection of two types of gadolinium with a 9.4-tesla micro-MRI.

MATERIALS AND METHODS

Gadolinium was injected into the middle ear in 6 Sprague-Dawley rats via the transtympanic route. The left ear was injected with Gd-DO3A-butrol first, and then the right ear was injected with Gd-DOTA. MR images of the inner ear were acquired 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, and 4 h after intratympanic (IT) injection using an Agilent MRI system 9.4T/160/AS. The normalized signal intensity was quantitatively analyzed at the scala vestibuli (SV), scala media, and scala tympani (ST) using a Marosis M-view system. Then the normalized signal intensities (SIs) were compared between the two contrast agents.

RESULTS

For Gd-DO3A-butrol, the SI was as low as 1.0-1.5 throughout 1-4 h at the SV and ST of the basal turn. The maximum SI was 1.5 ± 0.5 at the SV (2 h) and 1.3 ± 0.5 at the ST (2 h). For Gd-DOTA, the 1-hour postinjection SI at the basal turn was 2.5 ± 0.5 at the SV, 1.6 ± 0.3 at the ST, and 1.2 ± 0.3 at the scala media. In the apical turn, the maximum SI was reached after 2.5 h. The maximum SI in the apical turn was 1.8 ± 0.4 at the SV (3.5 h), 1.8 ± 0.4 at the ST (4 h), and 1.4 ± 0.3 at the scala media (4 h).

CONCLUSIONS

We were able to clearly visualize and separate the ST and SV using IT Gd and 9.4-tesla micro-MRI. We recommend using Gd-DO3A-butrol over Gd-DOTA and to perform the MRI 2.5 h after using IT Gd in the rat inner ear.

摘要

目的

使用9.4特斯拉微型磁共振成像(MRI)比较经鼓室内注射两种钆类造影剂后大鼠内耳外淋巴增强的质量。

材料与方法

通过经鼓室途径向6只Sprague-Dawley大鼠的中耳注射钆类造影剂。左耳先注射钆布醇(Gd-DO3A-butrol),然后右耳注射钆喷酸葡胺(Gd-DOTA)。使用安捷伦9.4T/160/AS MRI系统在鼓室内注射(IT)后1.0、1.5、2.0、2.5、3.0、3.5和4小时采集内耳的MR图像。使用Marosis M-view系统在前庭阶(SV)、中阶和鼓阶(ST)定量分析归一化信号强度。然后比较两种造影剂之间的归一化信号强度(SIs)。

结果

对于钆布醇,在基底部的SV和ST处,1至4小时内SI低至1.0 - 1.5。SV处(2小时)的最大SI为1.5±0.5,ST处(2小时)为1.3±0.5。对于钆喷酸葡胺,注射后1小时基底部的SV处SI为2.5±0.5,ST处为1.6±0.3,中阶为1.2±0.3。在顶段,2.5小时后达到最大SI。顶段的最大SI在SV处(3.5小时)为1.8±0.4,ST处(4小时)为1.8±0.4,中阶(4小时)为1.4±0.3。

结论

我们能够使用经鼓室注射钆类造影剂和9.4特斯拉微型MRI清晰地可视化并区分ST和SV。我们建议在大鼠内耳中使用钆布醇而非钆喷酸葡胺,并在经鼓室注射钆类造影剂后2.5小时进行MRI检查。

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