白质
磁共振成像
体内
磁共振光谱成像
老化
病理
高强度
神经影像学
神经科学
化学
核磁共振
核医学
医学
生物
内科学
放射科
遗传学
物理
作者
Virginie Lam,Juliette I. Phillips,Elizabeth Harrild,Rebecca J. Tidy,Ashley Hollings,Lincoln Codd,Kirsty Richardson,Liesl Celliers,Ryusuke Takechi,John C.L. Mamo,Mark J. Hackett
出处
期刊:Analyst
[Royal Society of Chemistry]
日期:2022-01-01
卷期号:147 (23): 5274-5282
被引量:1
摘要
Magnetic resonance imaging (MRI) is the gold standard method to study brain anatomy in vivo. Using MRI, subtle alterations to white matter structures in the brain are observed prior to cognitive decline associated with the ageing process, and neurodegenerative diseases such as Alzheimer's disease. Detection of such alterations provides hope for early clinical diagnosis. While MRI is essential to detect subtle alterations to brain structure in vivo, the technique is less suited to study and image the distribution of biochemical markers within specific brain structures. Consequently, the chemical changes that drive, or are associated with MRI-detectable alterations to white matter are not well understood. Herein, we describe (to the best of our knowledge) the first application of a complementary imaging approach that incorporates in vivo MRI with ex vivo Fourier transform infrared (FTIR) spectroscopic imaging on the same brain tissue. The combined workflow is used to detect and associate markers of altered biochemistry (FTIR) with anatomical changes to brain white matter (MRI). We have applied this combination of techniques to the senescence accelerated murine prone strain 8 (SAMP8) mouse model (n = 6 animals in each group, analysed across two ageing time points, 6 and 12 months). The results have demonstrated alterations to lipid composition and markers of disturbed metabolism during ageing are associated with loss of white matter volume.
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