[18F]氟替他莫在小鼠脑内的低摄取阻止髓磷脂的非侵入性定量

IF 4.9 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Molecular Pharmaceutics Pub Date : 2026-10-05 Epub Date: 2026-09-02 DOI:10.1021/acs.molpharmaceut.6c00470
Anna Schildt, Malena Beecken, Tobias Lindner, Markus Joksch, Jens Kurth, Marc-André Weber, Brigitte Vollmar, Bernd J. Krause, Sarah Joost
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引用次数: 0

摘要

髓磷脂的直接体内成像将极大地有利于脱髓鞘疾病(如多发性硬化症)的研究,但在技术上仍具有挑战性。本研究评价淀粉样蛋白-β放射性示踪剂[18F]氟替他莫是否适用于小鼠铜酮脱髓鞘模型的髓磷脂PET/CT成像。雄性C57BL/6小鼠连续5周(n = 5)喂食0.3%铜酮或对照组(n = 5),随后进行90分钟动态[18F]氟替他莫PET/CT扫描,2天后再次进行测试扫描。PET数据分析使用基于兴趣区域的量化与图像衍生的输入函数;分布体积(VT)通过Logan图形分析估计,并计算每毫升注射剂量百分比(% ID/mL)作为简化摄取措施。脱髓鞘独立通过MRI和组织学证实。铜普利酮治疗引起了显著的体重减轻和胼胝体区域特异性脱髓鞘,髓磷脂标记物表达减少,星形胶质细胞和小胶质细胞激活增加,以及相应的MRI变化证实了这一点。相比之下,体内[18F]氟替他莫PET表现出快速的放射性示踪剂冲洗,低脑潴留和高变异性。估计VT值非常低,在对照组和铜酮治疗小鼠之间没有差异。同样,% ID/mL在任何分析的大脑区域中都无法检测到组间差异,并且显示出很高的测试-重测试变异性。尽管组织学证实脱髓鞘和相应的t2加权MRI信号改变,[18F]氟替美莫PET/CT不能提供足够的灵敏度或定量稳健性来检测体内髓磷脂损失。这一阴性结果可能反映了示踪剂相关的局限性和方法学的局限性,包括有限的空间分辨率和定量建模的不确定性,因此不能得出关于氟替美莫在临床前髓磷脂成像中的内在适用性的明确结论[18F]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low Uptake of [18F]Flutemetamol in the Mouse Brain Prevents Non-invasive Quantification of Myelin

Direct in vivo imaging of myelin would greatly benefit research on demyelinating diseases such as multiple sclerosis but remains technically challenging. This study evaluated whether the amyloid-β radiotracer [18F]Flutemetamol is suitable for PET/CT imaging of myelin in the murine cuprizone model of demyelination. Male C57BL/6 mice were fed 0.3% cuprizone for five weeks (n = 5) or control chow (n = 5) and subsequently underwent a 90 min dynamic [18F]Flutemetamol PET/CT scan with a retest scan two days later. PET data were analyzed using region-of-interest-based quantification with an image-derived input function; volume of distribution (VT) was estimated by Logan graphical analysis, and percentage injected dose per milliliter (% ID/mL) was calculated as a simplified uptake measure. Demyelination was independently validated by MRI and histology. Cuprizone treatment induced significant body weight loss and robust region-specific demyelination of the corpus callosum, confirmed by reduced myelin marker expression, increased astroglial and microglial activation, and corresponding MRI changes. In contrast, in vivo [18F]Flutemetamol PET showed rapid radiotracer washout, low brain retention, and high variability. Estimated VT values were very low and did not differ between control and cuprizone-treated mice. Similarly, % ID/mL failed to detect group differences in any analyzed brain region and showed high test−retest variability. Despite histologically confirmed demyelination and corresponding T2-weighted MRI signal alterations, [18F]Flutemetamol PET/CT did not provide sufficient sensitivity or quantitative robustness to detect myelin loss in vivo. This negative finding might reflect a combination of tracer-related and methodological limitations, including limited spatial resolution and uncertainties in quantitative modeling, and therefore does not allow a definitive conclusion regarding the intrinsic suitability of [18F]Flutemetamol for preclinical myelin imaging.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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