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Neuroprotective effects of beta-secretase inhibitors against rat retinal ganglion cell death.

机译:β-分泌酶抑制剂对大鼠视网膜神经节细胞死亡的神经保护作用。

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摘要

Beta-secretase, an enzyme participating in amyloid beta-peptide generation, is thought to be involved in the pathogenesis of Alzheimer's disease. We examined the effects of beta-secretase inhibitors such as N-benzyloxycarbonyl-Val-Leu-leucinal (Z-VLL-CHO) and H-EVNstatineVAEF-NH2 (GL-189) on glutamate-induced retinal ganglion cell (RGC) death in vitro. In cultures of purified RGCs from neonatal rats, 2-day exposure to 25 microM glutamate induced RGC death, and Z-VLL-CHO (100 nM) and GL-189 (1 microM) had neuroprotective effects. We also found out that Z-VLL-CHO showed a neuroprotective effect on retinal damage induced by optic nerve crush in vivo. Thus, beta-secretase could be a potential target for therapy of neurodegenerative retinal diseases.
机译:β-分泌酶,一种参与淀粉样β-肽生成的酶,被认为与阿尔茨海默氏病的发病机理有关。我们检查了诸如N-苄氧基羰基-Val-Leu-亮氨酸(Z-VLL-CHO)和H-EVNstatineVAEF-NH2(GL-189)等β-分泌酶抑制剂对谷氨酸诱导的视网膜神经节细胞(RGC)死亡的影响体外。在来自新生大鼠的纯化RGC的培养物中,暴露于25 microM谷氨酸的2天暴露导致RGC死亡,Z-VLL-CHO(100 nM)和GL-189(1 microM)具有神经保护作用。我们还发现Z-VLL-CHO对体内由视神经挤压引起的视网膜损伤具有神经保护作用。因此,β-分泌酶可能是神经退行性视网膜疾病治疗的潜在目标。

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