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首页> 外文期刊>Experimental Eye Research >Demyelination and shrinkage of axons in the retinal nerve fiber layer in chickens developing deprivation myopia
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Demyelination and shrinkage of axons in the retinal nerve fiber layer in chickens developing deprivation myopia

机译:显性神经纤维层中鸡氏症中缺乏近视的脱髓鞘和收缩

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Placing diffusers in front of the eyes induces deprivation myopia in a variety of animal models. As a result of the low pass filtering of the retinal images, less spatial information is available to the retina which should reduce neural activity. Since it has been found that myelination of axons in the central nervous system is modulated by neuronal activity, we have studied whether ganglion cell axons may shrink in response to the restricted visual input. Young chickens were treated for 5 h or 7 days with frosted diffusers to induce deprivation myopia. Nerve fiber layer thickness was measured in vivo, using B-scan OCT. Refractive states were tracked by IR photoretinoscopy, and UV fundus reflectivity by a custom-built device which flashed an LED centered in the camera aperture and recorded pupil brightness after refractive errors were corrected by trial lenses. Moreover, structure and histology of the retinal nerve fibers layer (RNFL) were analyzed ex vivo using transmission electron microscopy and immunohistochemistry. Since chicks have both non-myelinated and myelinated fibers in their RNFL, the thickness of myelin sheaths (G ratio) was measured, as well as the percentage of myelinated axons and the diameters of unmyelinated axons. Short-term deprivation caused an increase in UV fundus reflectivity already after 5 h (measured as pixel grey levels in the pupil: 28 +/- 5 vs. 36 +/- 10, p < 0.05) and thinning of the myelin sheaths (higher G ratio), compared to untreated control eyes (0.74 +/- 0.01 vs. 0.79 +/- 0.03, p < 0.05). Neither axon diameters (0.81 +/- 0.05 mu m vs,-0.82 +/- 0.15 mu m) nor thickness of the RNFL had changed after only 5 h (42.9 +/- 1.3 mu m vs. 42.3 +/- 2.5 mu m). However, after 7 days of diffuser wear, axons had become thinner (0.56 +/- 0.14 mu m vs. 0.78 +/- 0.09 mu m vs, p < 0.05), which could explain the thinning of the RNFL (36.3 +/- 2.7 mu m vs. 42.1 +/- 2.4 mu m, p < 0.01). Furthermore, myopic eyes had 38% less myelinated axons than untreated eyes as determined by immunohistochemical labelling against myelin basic protein (immunopositive areas in the central retina 1406 +/- 341 mu m(2) vs. 2185 +/- 290 mu m(2) in controls, p < 0.001). Myelin sheaths in the remaining axons remained unchanged (G ratio 0.76 +/- 0.02 vs. 0.76 +/- 0.03). Our study shows that deprivation myopia is associated with a significant loss of myelinated axons and shrinkage of the axon diameters of certain fibers in the RNFL. Early changes were already detected after 5 h and were accompanied by an increased fundus reflectivity in UV light. These parameters could therefore serve as the biomarkers for myopia development, at least in the chicken.
机译:将漫射器放在眼前的焦点诱导剥夺近视在各种动物模型中。由于视网膜图像的低通滤波,视网膜可获得较少的空间信息,这应该减少神经活动。由于已发现中枢神经系统中的轴突中的髓鞘由神经元活动调节,我们研究了神经节细胞轴突是否可能响应受限的视觉输入而缩小。用磨砂的扩散器治疗幼小鸡5小时或7天,以诱导剥夺近视。使用B扫描OCT在体内测量神经纤维层厚度。 IR光致抑制仪跟踪折射率,通过定制装置的UV眼底反射率,该装置闪烁在相机孔径中闪烁的LED,并通过试验镜头校正折射误差后记录瞳孔亮度。此外,使用透射电子显微镜和免疫组化分析视网膜神经纤维层(RNFL)的结构和组织学。由于雏鸡在其RNFL中具有非髓鞘和髓鞘纤维,因此测量髓鞘(G比率)的厚度,以及密骨化轴突的百分比和未键合的轴突的直径。短期剥夺导致5小时后的UV眼底反射率增加(以瞳孔中的像素灰度水平测量:28 +/- 5与36 +/- 10,P <0.05)和髓鞘的稀疏(更高与未处理的对照眼相比,G比)(0.74 +/- 0.01,0.79 +/- 0.03,P <0.05)。在仅5小时后,轴突直径(0.81 +/- 0.05 mu m vs,-0.82 +/- 0.15 mu m)也没有改变(42.9 +/- 1.3 mu m vs.2.3 +/- 2.5 mu m )。但是,在漫射7天后,轴突变薄(0.56 +/- 0.14 mu m vs. 0.78 +/- 0.09 mu m vs,p <0.05),可以解释RNFL的变薄(36.3 +/- 2.7 mu m vs. 42.1 +/- 2.4 mu m,p <0.01)。此外,近视眼的弱眼臂具有38%,而不是通过免疫组织化学标记针对髓鞘碱性蛋白质(中央视网膜1406 +/-341μm(2)的免疫阳性区域的影响而确定(2)(2 )在对照中,p <0.001)。剩余轴突中的髓鞘保持不变(G比率0.76 +/- 0.02对0.76 +/- 0.03)。我们的研究表明,剥夺近视与RNFL中的某些纤维的轴突直径的显着损失有关。在5小时后已经检测到早期的变化,并伴随着UV光线的增加的眼底反射率。因此,这些参数可以作为近视发展的生物标志物,至少在鸡中。

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