University of Alabama at Birmingham, School of Optometry, 1716 University Blvd, Birmingham, AL, USA.
Nationwide Children's Hospital, Center for Clinical and Translational Research, 700 Childrens Drive, Columbus, OH, USA.
Exp Eye Res. 2020 Apr;193:107963. doi: 10.1016/j.exer.2020.107963. Epub 2020 Feb 8.
Myopic children have larger ciliary muscles than non-myopic children, suggesting that the ciliary muscle may have an impact on or be affected by refractive error development. The guinea pig represents an attractive model organism for myopia development research. The purpose of the study was to investigate whether form deprivation-induced myopia in one or more strains of guinea pig causes thickening of the ciliary muscle as seen in human myopia. Thirty-nine guinea pigs were bred from in-house progenitors obtained from Cincinnati Children's Hospital (Cincinnati) and the United States Army (Strain 13). At 2-4 days of age the right eyes of animals were exposed to form deprivation for 7 days while the fellow eyes served as controls. Refractive error was determined with retinoscopy while vitreous chamber depth (VCD) and axial length (AL) were determined with A-scan ultrasound. Ciliary muscle characteristics (ciliary muscle length, cross-sectional area, volume, cell number, cell size, and smooth muscle actin concentration) were determined histologically with antibody labeling and analyzed according to whether the animal developed axial myopia (anisometropia > -2.00 D with VCD and/or AL differences > 0.1 mm) or was unresponsive. This analysis method yielded four groups with Group 1 having no induced myopia but with axial elongation (n = 11), Group 2 having myopia without vitreous or axial elongation (n = 8), Group 3 having myopia with either vitreous or axial elongation (n = 11), and Group 4 having myopia with both vitreous and axial elongation (n = 8). There were no post-treatment inter-ocular differences between strains or for the overall group of animals for any ciliary muscle variable; however, a higher response group number in multivariate ordinal regression was related to having a treated compared to fellow eye that had a lower smooth muscle actin concentration (p = 0.006), with a shorter ciliary muscle length (p = 0.042), and a less oblate eye shape (p = 0.010). Guinea pig ciliary muscle length and smooth muscle actin concentration were significantly less in the treated eyes of axially myopic animals suggesting that 7 days of form deprivation induced ciliary muscle cellular atrophy or inhibited ciliary muscle growth. Form deprivation myopia in the guinea pig does not result in the increase in ciliary muscle thickness associated with human juvenile and adult myopia.
近视儿童的睫状肌比非近视儿童的大,这表明睫状肌可能对屈光不正的发展有影响或受其影响。豚鼠是研究近视发展的一个很有吸引力的模式生物。本研究的目的是探讨一种或多种豚鼠品系的形觉剥夺性近视是否会导致像人类近视那样的睫状肌增厚。39 只豚鼠由辛辛那提儿童医院(辛辛那提)和美国陆军(品系 13)的内部后代繁殖而来。在 2-4 天大时,动物的右眼接受 7 天的形觉剥夺,而对侧眼作为对照。通过视网膜检影术确定屈光不正,通过 A 型超声确定玻璃体腔深度(VCD)和眼轴长度(AL)。用抗体标记法对睫状肌特征(睫状肌长度、横截面积、体积、细胞数、细胞大小和平滑肌肌动蛋白浓度)进行组织学检测,并根据动物是否发生轴向性近视(VCD 和/或 AL 差异>0.1mm 时的屈光参差> -2.00D)或无反应进行分析。这种分析方法产生了四组,第 1 组无诱导性近视但轴向伸长(n=11),第 2 组有近视但无玻璃体或轴向伸长(n=8),第 3 组有近视但有玻璃体或轴向伸长(n=11),第 4 组有近视且玻璃体和轴向伸长(n=8)。在任何睫状肌变量方面,各组之间或动物的总体之间在治疗后均无眼间差异;然而,多变量有序回归中较高的反应组数量与治疗眼的平滑肌肌动蛋白浓度较低(p=0.006)、睫状肌长度较短(p=0.042)和眼球形状更扁有关(p=0.010)。轴向近视动物的治疗眼的豚鼠睫状肌长度和平滑肌肌动蛋白浓度显著降低,提示 7 天的形觉剥夺诱导睫状肌细胞萎缩或抑制睫状肌生长。豚鼠的形觉剥夺性近视不会导致与人类青少年和成年近视相关的睫状肌厚度增加。