Centre de Biophysique Moléculaire, CNRS , rue Charles Sadron, 45071 Orléans, Cedex 2, France.
ACS Chem Neurosci. 2015 Feb 18;6(2):219-25. doi: 10.1021/cn500289y. Epub 2014 Dec 19.
Molecular magnetic resonance imaging (MRI) approaches that detect biomarkers associated with neural activity would allow more direct observation of brain function than current functional MRI based on blood-oxygen-level-dependent contrast. Our objective was to create a synthetic molecular platform with appropriate recognition moieties for zwitterionic neurotransmitters that generate an MR signal change upon neurotransmitter binding. The gadolinium complex (GdL) we report offers ditopic binding for zwitterionic amino acid neurotransmitters, via interactions (i) between the positively charged and coordinatively unsaturated metal center and the carboxylate function and (ii) between a triazacrown ether and the amine group of the neurotransmitters. GdL discriminates zwitterionic neurotransmitters from monoamines. Neurotransmitter binding leads to a remarkable relaxivity change, related to a decrease in hydration number. GdL was successfully used to monitor neural activity in ex vivo mouse brain slices by MRI.
分子磁共振成像(MRI)方法可以检测与神经活动相关的生物标志物,这将比目前基于血氧水平依赖对比的功能 MRI 更直接地观察大脑功能。我们的目标是创建一个具有适当识别部分的合成分子平台,用于带有正电荷和配位不饱和金属中心的两性离子氨基酸神经递质的相互作用 (i) 和三氮杂冠醚与神经递质的胺基之间的相互作用 (ii)。GdL 区分两性离子神经递质和单胺。神经递质结合导致显著的弛豫率变化,与水合数的减少有关。GdL 成功地用于通过 MRI 监测离体小鼠脑片的神经活动。