Rabin O, Hegedus L, Bourre J M, Smith Q R
Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health, Bethesda, Maryland 20892.
J Neurochem. 1993 Aug;61(2):509-17. doi: 10.1111/j.1471-4159.1993.tb02153.x.
54Mn2+ uptake into brain and choroid plexus from the circulation was studied using the in situ rat brain perfusion technique. Initial uptake from blood was linear with time (30 s to 6 min) and extrapolated to zero with an average transfer coefficient of approximately 6 x 10(-5) ml/s/g for brain and approximately 7 x 10(-3) ml/s/g for choroid plexus. Influx from physiologic saline was three- to fourfold more rapid and exceeded that predicted for passive diffusion by more than one order of magnitude. The lower uptake rate from blood could be explained by plasma protein binding as the free fraction of 54Mn2+ in rat plasma was < or = 30%. Purified albumin, transferrin, and alpha 2-macroglobulin were each found to bind 54Mn2+ significantly and to restrict brain 54Mn2+ influx. The results demonstrate that 54Mn2+ is readily taken up into the CNS, most likely as the free ion, and that transport is critically affected by plasma protein binding. The results support the hypothesis that Mn2+ transport across the blood-brain barrier is facilitated by either an active or a passive mechanism.
采用原位大鼠脑灌注技术研究了54Mn2+从循环系统进入脑和脉络丛的情况。血液中的初始摄取与时间呈线性关系(30秒至6分钟),外推至零时,脑的平均转运系数约为6×10(-5)毫升/秒/克,脉络丛约为7×10(-3)毫升/秒/克。从生理盐水的流入速度快三到四倍,且超过被动扩散预测值一个多数量级。血液摄取率较低可由血浆蛋白结合来解释,因为大鼠血浆中54Mn2+的游离部分≤30%。发现纯化的白蛋白、转铁蛋白和α2-巨球蛋白均能显著结合54Mn2+并限制脑54Mn2+的流入。结果表明,54Mn2+很容易进入中枢神经系统,最有可能是以游离离子形式,并且转运受到血浆蛋白结合的严重影响。这些结果支持了Mn2+通过主动或被动机制促进穿过血脑屏障转运的假说。