Developmental trajectory of magnetic susceptibility in the healthy rhesus macaque brain

定量磁化率图 壳核 苍白球 恒河猴 尾状核 黑质 齿状核 丘脑 猕猴 红核 人脑 神经科学 生物 病理 基底神经节 核心 磁共振成像 中枢神经系统 医学 小脑 多巴胺 免疫学 多巴胺能 放射科
作者
Jing Wu,Siyue Peng,Yuhua Zhang,Boyang Pan,Honghua Chen,Xintian Hu,Nan‐Jie Gong
出处
期刊:NMR in Biomedicine [Wiley]
卷期号:35 (9): e4750-e4750 被引量:2
标识
DOI:10.1002/nbm.4750
摘要

Quantitative susceptibility mapping (QSM) is used to quantify iron deposition in non‐human primates in our study. Although QSM has many applications in detecting iron deposits in the human brain, including the distribution of iron deposits in specific brain regions, the change of iron deposition with aging, and the comparison of iron deposits between diseased groups and healthy controls, few studies have applied QSM to non‐human primates, while most animal brain experiments focus on biochemical and anatomical results instead of non‐invasive experiments. Additionally, brain imaging in children's research is difficult, but can be substituted using young rhesus monkeys, which are very similar to humans, as research animals. Therefore, understanding the relationship between iron deposition and age in rhesus macaques' brains can offer insights into both the developmental trajectory of magnetic susceptibility in the animal model and the correlated evidence in children's research. Twenty‐three healthy rhesus macaque monkeys (23 ± 7.85 years, range 2–29 years) were included in this research. Seven regions of interest (ROIs—globus pallidus, substantia nigra, dentate nucleus, caudate nucleus, putamen, thalamus, red nucleus) have been analyzed in terms of QSM and R 2 * (apparent relaxation rate). Susceptibility in most ROIs correlated significantly with the growth of age, similarly to the results for R 2 *, but showed different trends in the thalamus and red nucleus, which may be caused by the different sensitivities of myelination and iron deposition in R 2 * and QSM analysis. By assessing the correlation between iron content and age in healthy rhesus macaques' brains using QSM, we provide a piece of pilot information on normality for advanced animal disease models. Meanwhile, this study also could serve as the normative basis for further clinical studies using QSM for iron content quantification. Due to the comparison of the susceptibility on the same experimental objects, this research can also provide practical support for future research on characteristics for QSM and R 2 *.
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