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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Neuroprotection of adult rat dorsal root ganglion neurons by combined hypothermia and alkalinization against prolonged ischemia.
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Neuroprotection of adult rat dorsal root ganglion neurons by combined hypothermia and alkalinization against prolonged ischemia.

机译:联合低温和碱化对成年大鼠背根神经节神经元的神经保护作用,以防止长时间缺血。

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摘要

Ischemia and ischemia-induced secondary events, such as acidosis and excessive activation of receptors by amino acids, trigger neuron death. The isolation and dissociation of dorsal root ganglion (DRG) involves time during which the neurons are ischemic due to being densely packed within the intact DRG and surrounded by a connective tissue coat. Thus, the longer the time between killing the host animal and when the DRG are dissociated, the longer the neurons are ischemic and exposed to ischemia-induced secondary causes of neuron death. It is well established that hypothermia and alkalinization each separately protect neurons from ischemia and ischemia-induced secondary causes of neuron death, but there are no data on the neuroprotection provided by simultaneous hypothermia and alkalinization. The present experiments were designed to determine the combination of hypothermic and alkaline conditions that yield the largest number of viable neurons dissociated from intact DRG maintained ischemic for up to 4h. Hypothermia (20 degrees C>15 degrees C>37 degrees C) and alkalinization (pH 9.3>pH 8.3>pH 7.4) increased the yield of viable neurons compared with the yield from DRG maintained under physiological conditions. Hypothermia and alkalinization combined (20 degrees C/pH 9.3) provided the greatest neuroprotection with a yield of viable neurons after 1 h of ischemia 2.5-fold larger than that from DRG maintained under physiological conditions (37 degrees C/pH 7.6). Over 4 h of ischemia, the yield of viable neurons from DRG maintained under both hypothermic/alkaline and physiological conditions decreased in a linear manner, but those at 20 degrees C/pH 9.3 had a 4.5-fold greater yield of viable neurons than those at 37 degrees C/pH 7.6. Thus, combined hypothermia and alkalinization provide significantly greater protection against ischemia and ischemia-induced secondary causes of neuron death than either alone.
机译:缺血和局部缺血引起的继发性事件,例如酸中毒和氨基酸对受体的过度激活,会触发神经元死亡。背根神经节(DRG)的分离和解离涉及到神经元缺血的时间,这是由于神经元被密集地包裹在完整的DRG中并被结缔组织涂层包围。因此,杀死宿主动物与解离DRG之间的时间越长,神经元缺血的时间就越长,并暴露于缺血诱导的神经元死亡的继发性原因中。公认的是,低温和碱化分别分别保护神经元免受缺血和缺血诱导的神经元死亡的继发性原因,但是没有同时低温和碱化提供的神经保护数据。本实验旨在确定低温条件和碱性条件的组合,该条件可产生从完整的DRG维持缺血长达4小时解离的最大数量的存活神经元。与生理条件下维持DRG的产量相比,低温(20°C> 15°C> 37°C)和碱化(pH 9.3> pH 8.3> pH 7.4)增加了存活神经元的产量。低温和碱化相结合(20摄氏度/ pH 9.3)可提供最大的神经保护作用,缺血1小时后的存活神经元产量比生理条件下维持的DRG(37摄氏度/ pH 7.6)高2.5倍。在缺血4小时以上,在低温/碱性和生理条件下维持的DRG存活神经元的产量均呈线性下降,但在20摄氏度/ pH 9.3的条件下,DRG存活神经元的产量比在7.5倍时高4.5倍。 37℃/ pH 7.6。因此,与单独使用低温和碱化相结合,对缺血和缺血引起的神经元死亡的继发原因的保护作用明显增强。

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