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首页> 外文期刊>Clinical and experimental ophthalmology >Neuropeptide Y expression in a mouse model of oxygen-induced retinopathy.
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Neuropeptide Y expression in a mouse model of oxygen-induced retinopathy.

机译:氧致视网膜病变的小鼠模型中的神经肽Y表达。

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摘要

BACKGROUND: Neuropeptide Y (NPY) is a potent vaso-constrictor and angiogenic agent that is found in the retina. The goal of this study was to determine the expression of NPY and its receptors, NPY Y1 and NPY Y2, in a mouse model of oxygen-induced retinopathy. METHODS: Retinal NPY, NPY Y1, and NPY Y2 mRNA expression were evaluated using reverse transcriptase-polymerase chain reaction. Neuropeptide Y cellular localization was determined using immunohistochemistry. RESULTS: Retinal NPY mRNA expression was increased by 2.3-fold from P7 to P12, and 2.8-fold from P7 to P17 in oxygen-reared animals. Retinal NPY Y1 was increased 1.9-fold from P7 to P12 in room-air-reared animals. There was no change in NPY Y1 expression following exposure to oxygen. Retinal NPY Y2 expression in oxygen-reared animals increased by 2.8-fold from P7 to P12 and by 2.7-fold from P12 to P17. There was no change in NPY Y2 expression in room-air-reared animals. Retinal NPY and NPY Y2 expression increased concomitant with vasoconstriction and neovascularization seen in this model by evaluation of retinal whole mounts. Neuropeptide Y protein was detectable by immunohistochemistry mainly between the inner and outer nuclear layers and increased with hyperoxic exposure at P12 and also increased during the period of relative retinal hypoxia at P17. CONCLUSIONS: Retinal NPY and NPY Y2 receptor expression are altered in the development of oxygen-induced retinopathy of the mouse, during both the hyperoxic vasoconstrictive phase and the period of retinal neovascularization. Alteration in the production of NPY and the NPY Y2 receptor may be avenues for potential modification in the development of retinopathy.
机译:背景:神经肽Y(NPY)是一种有效的血管收缩剂和血管生成剂,存在于视网膜中。这项研究的目的是确定在氧致视网膜病变的小鼠模型中NPY及其受体NPY Y1和NPY Y2的表达。方法:采用逆转录聚合酶链反应评估视网膜NPY,NPY Y1和NPY Y2 mRNA的表达。使用免疫组织化学测定神经肽Y的细胞定位。结果:在饲养氧气的动物中,视网膜NPY mRNA的表达从P7到P12增加了2.3倍,从P7到P17增加了2.8倍。在室内饲养的动物中,视网膜NPY Y1从P7增加到P12 1.9倍。暴露于氧气后,NPY Y1表达没有变化。从P7到P12,氧气喂养动物的视网膜NPY Y2表达增加了2.8倍,从P12到P17增加了2.7倍。在饲养室内空气的动物中,NPY Y2表达没有变化。通过评估视网膜的整个坐骑,在该模型中看到的视网膜NPY和NPY Y2表达增加与血管收缩和新血管形成同时发生。神经肽Y蛋白主要通过内,外核层之间的免疫组织化学检测到,并在P12处随着高氧暴露而增加,并且在P17处的相对视网膜缺氧期间也增加。结论:在高氧血管收缩期和视网膜新生血管形成期间,氧诱导的小鼠视网膜病变的发展过程中,视网膜NPY和NPY Y2受体的表达均发生了改变。 NPY和NPY Y2受体产生的改变可能是视网膜病发展中潜在修饰的途径。

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