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首页> 外文期刊>Scientific reports. >Effects of BNN27, a novel C17-spiroepoxy steroid derivative, on experimental retinal detachment-induced photoreceptor cell death
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Effects of BNN27, a novel C17-spiroepoxy steroid derivative, on experimental retinal detachment-induced photoreceptor cell death

机译:新型C17-螺环氧类固醇衍生物BNN27对实验性视网膜脱离诱导的感光细胞死亡的影响

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Retinal detachment (RD) leads to photoreceptor cell death secondary to the physical separation of the retina from the underlying retinal pigment epithelium. Intensifying photoreceptor survival in the detached retina could be remarkably favorable for many retinopathies in which RD can be seen. BNN27, a blood-brain barrier (BBB)-permeable, C17-spiroepoxy derivative of dehydroepiandrosterone (DHEA) has shown promising neuroprotective activity through interaction with nerve growth factor receptors, TrkA and p75NTR. Here, we administered BNN27 systemically in a murine model of RD. TUNEL+ photoreceptors were significantly decreased 24?hours post injury after a single administration of 200?mg/kg BNN27. Furthermore, BNN27 increased inflammatory cell infiltration, as well as, two markers of gliosis 24?hours post RD. However, single or multiple doses of BNN27 were not able to protect the overall survival of photoreceptors 7 days post injury. Additionally, BNN27 did not induce the activation/phosphorylation of TrkAY490 in the detached retina although the mRNA levels of the receptor were increased in the photoreceptors post injury. Together, these findings, do not demonstrate neuroprotective activity of BNN27 in experimentally-induced RD. Further studies are needed in order to elucidate the paradox/contradiction of these results and the mechanism of action of BNN27 in this model of photoreceptor cell damage.
机译:视网膜脱离(RD)导致继视网膜与下面的视网膜色素上皮细胞物理分离后继发的感光细胞死亡。对于许多可以看到RD的视网膜病,增加视网膜脱离时感光细胞的存活可能会非常有利。 BNN27是一种脱氢表雄酮(DHEA)的血脑屏障(BBB)渗透性,C17-螺氧基环氧衍生物(DHEA),通过与神经生长因子受体,TrkA和p75NTR相互作用,显示出有希望的神经保护活性。在这里,我们在RD的小鼠模型中全身性施用BNN27。单次给予200?mg / kg BNN27后,损伤后24小时TUNEL +感光细胞显着下降。此外,BNN27增加了炎症细胞浸润,以及RD后24小时出现的两种胶质细胞增生标志物。但是,单剂量或多剂量的BNN27不能在损伤后7天保护感光细胞的整体存活。另外,尽管损伤后感光细胞中受体的mRNA水平增加,但BNN27并未在分离的视网膜中诱导TrkAY490的激活/磷酸化。总之,这些发现并未证明BNN27在实验诱导的RD中具有神经保护活性。为了阐明这些结果的矛盾/矛盾以及在这种感光细胞损伤模型中BNN27的作用机理,需要进一步的研究。

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