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首页> 外文期刊>CNS neuroscience & therapeutics. >REVIEW: An Approach for Neuroprotective Therapies of Secondary Brain Damage after Excitotoxic Retinal Injury in Mice
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REVIEW: An Approach for Neuroprotective Therapies of Secondary Brain Damage after Excitotoxic Retinal Injury in Mice

机译:综述:小鼠兴奋性视网膜毒性损伤后继发性脑损伤的神经保护治疗方法

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SUMMARY Background: Many current therapeutic strategies for several eye diseases, such as glaucoma, retinal ischemia, and optic neuropathy, are focused on protection of the retinal ganglion cells (RGCs). In fact, loss of visual field, including irreversible blindness, is caused by RGC damage in these diseases. However, recent evidence suggests that the RGC damage extends to visual center in brain: the visual impairment induced by these diseases may result not only from RGC loss, but also from neuronal degeneration within the visual center in brain. Objective: To protect neurons within the visual center in the brain, as well as retinal treatment, for the prevention of visual disorder in these diseases. Methods: Once considered difficult to study the visual center in brain following RGCs loss, because obtaining the human samples that are suitable for the study may be difficult. In addition, the monkey, mainly used as glaucomatous model, is relatively high cost and needs to long experiment‐span. Here, we focused on mice, because of their high degree of availability, relatively low cost, and amenability to experimental and genetic manipulation. Conclusion: In this review, we describe time‐dependent alterations in the visual center in brain following RGCs loss, and whether some drugs prevent the neuronal damage of the visual center in the brain.
机译:发明内容背景:对于几种眼疾病,例如青光眼,视网膜缺血和视神经病变,许多当前的治疗策略集中于保护视网膜神经节细胞(RGC)。实际上,这些疾病的RGC损害会导致视野丧失,包括不可逆转的失明。但是,最近的证据表明,RGC的损害扩展到了大脑的视觉中心:这些疾病引起的视觉障碍可能不仅是由于RGC的丧失,还可能是由于大脑视觉中心内的神经元变性所致。目的:保护脑部视觉中心内的神经元以及视网膜治疗,以预防这些疾病的视觉障碍。方法:曾经认为研究RGC丢失后很难研究大脑的视觉中心,因为获得适合该研究的人体样品可能很困难。此外,主要用作青光眼模型的猴子成本较高,需要较长的实验时间。在这里,我们将重点放在小鼠上,因为它们具有较高的可用性,相对较低的成本以及对实验和基因操作的适应性。结论:在这篇综述中,我们描述了RGC丢失后大脑视力中心的时间依赖性变化,以及某些药物是否能预防大脑视力中心的神经元损伤。

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