Section on Neural Gene Expression, National Institute of Mental Health, National Institutes of Health, DHHS, 9000 Rockville Pike, Building 49, Room 5A51, Bethesda, MD 20892-4483, USA.
Brain Struct Funct. 2012 Jan;217(1):107-14. doi: 10.1007/s00429-011-0324-y. Epub 2011 May 20.
Manganese-enhanced magnetic resonance imaging is a technique that employs the divalent ion of the paramagnetic metal manganese (Mn(2+)) as an effective contrast agent to visualize, in vivo, the mammalian brain. As total achievable contrast is directly proportional to the net amount of Mn(2+) accumulated in the brain, there is a great interest in optimizing administration protocols to increase the effective delivery of Mn(2+) to the brain while avoiding the toxic effects of Mn(2+) overexposure. In this study, we investigated outcomes following continuous slow systemic infusion of manganese chloride (MnCl(2)) into the mouse via mini-osmotic pump administration. The effects of increasing fractionated rates of Mn(2+) infusion on signal enhancement in regions of the brain were analyzed in a three-treatment study. We acquired whole-brain 3-D T1-weighted images and performed region of interest quantitative analysis to compare mean normalized signal in Mn(2+) treatments spanning 3, 7, or 14 days of infusion (rates of 1, 0.5, and 0.25 μL/h, respectively). Evidence of Mn(2+) transport at the conclusion of each infusion treatment was observed throughout the brains of normally behaving mice. Regions of particular Mn(2+) accumulation include the olfactory bulbs, cortex, infralimbic cortex, habenula, thalamus, hippocampal formation, amygdala, hypothalamus, inferior colliculus, and cerebellum. Signals measured at the completion of each infusion treatment indicate comparable means for all examined fractionated rates of Mn(2+) infusion. In this current study, we achieved a significantly higher dose of Mn(2+) (180 mg/kg) than that employed in previous studies without any observable toxic effects on animal physiology or behavior.
锰增强磁共振成像是一种技术,它使用顺磁性金属锰(Mn(2+))的二价离子作为有效的对比剂,在体内可视化哺乳动物的大脑。由于总可实现的对比度与在大脑中积累的 Mn(2+)的净量成正比,因此人们非常感兴趣的是优化给药方案,以增加 Mn(2+)向大脑的有效传递,同时避免 Mn(2+)过度暴露的毒性作用。在这项研究中,我们通过迷你渗透泵给药,研究了连续缓慢全身输注氯化锰(MnCl(2))对小鼠的结果。在三处理研究中,分析了增加 Mn(2+)输注分馏率对大脑区域信号增强的影响。我们采集了全脑 3-D T1 加权图像,并进行了感兴趣区域的定量分析,以比较跨越 3、7 或 14 天输注的 Mn(2+)处理的平均归一化信号(分别为 1、0.5 和 0.25 μL/h 的速率)。在正常行为小鼠的大脑中,观察到每个输注处理结束时 Mn(2+)转运的证据。特别 Mn(2+)积累的区域包括嗅球、皮质、下边缘皮层、缰核、丘脑、海马结构、杏仁核、下丘脑、下丘和小脑。在每个输注处理完成时测量的信号表明,所有检查的 Mn(2+)输注分馏率的平均值都相当。在这项当前的研究中,我们实现了比以前的研究更高的 Mn(2+)剂量(180mg/kg),而对动物生理或行为没有任何可观察到的毒性作用。