Gao Qianying, Liu Quan, Ma Ping, Zhong XingWu, Wu Junshu, Ge Jian
Key Laboratory of Ophthalmology, Ministry of Education, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, 510060, People's Republic of China.
Graefes Arch Clin Exp Ophthalmol. 2006 Oct;244(10):1329-35. doi: 10.1007/s00417-006-0254-1. Epub 2006 Mar 21.
Dopamine (DA) storage and release are reduced in form deprivation myopia (FDM) in a wide range of species, from chicks to primates. FDM can be prevented by treatment with DA agonists such as apomorphine, and paradoxically by the dopamine neurotoxin 6-hydroxydopamine. In this study, we increased the DA levels by direct intravitreal DA injections to learn if FDM can be suppressed in a rabbit model.
Seven-day-old rabbits were deprived of pattern vision by the suturing the right eyelids after natural eye opening. In the first group (FD, n=20), the right eye received form deprivation (FD) alone. In the second group (DA-FD, n=16), the deprived eye of 7-day-old rabbits received four intravitreal injections of 20 microg dopamine every 5 days. In the third group (saline-FD, n=16), the deprived eye received saline injections with the same schedule. The contralateral eye remained untreated as a control. At the end of the 8-week deprivation period, the effects of DA on refractive error, corneal curvature and ocular dimensions were assessed by streak retinoscopy, keratometry and A-scan ultrasonography, respectively.
Eight weeks of FDM induced a myopic shift of -2.70+/-0.87 D (n=20) in treated eyes compared with contralateral eyes. The major structural correlate of the myopia appeared to be elongation of the vitreous chamber (0.7+/-0.3 mm, n=20) and axial elongation (0.9+/-0.3 mm, n=20), respectively. Repeated intravitreal injections of DA fully prevented the myopic shift (-0.06+/-0.37 D), elongation of the vitreous chamber (0.1+/-0.3 mm, n=16) and axial elongation (0.3+/-0.2 mm, n=16) due to lid suture, whereas saline injections had slight effect.
FD by suturing eyelids is an effective technique to induce a significant myopic shift, vitreous chamber and axial elongation in rabbits as a model of myopia development. These changes associated with FD were retarded by intravitreal injections of DA.
从雏鸡到灵长类等多种物种的形觉剥夺性近视(FDM)中,多巴胺(DA)的储存和释放均减少。FDM可通过阿扑吗啡等DA激动剂治疗来预防,而多巴胺神经毒素6-羟基多巴胺却能产生相反的效果。在本研究中,我们通过直接玻璃体内注射DA来提高DA水平,以了解在兔模型中FDM是否能够被抑制。
7日龄兔在自然睁眼后缝合右眼眼睑以剥夺形觉。第一组(FD组,n = 20),右眼仅接受形觉剥夺(FD)。第二组(DA - FD组,n = 16),7日龄兔的被剥夺眼每5天接受4次20μg多巴胺的玻璃体内注射。第三组(生理盐水 - FD组,n = 16),被剥夺眼按相同方案接受生理盐水注射。对侧眼不做处理作为对照。在8周剥夺期结束时,分别通过带状检影法、角膜曲率测量法和A超超声检查评估DA对屈光不正、角膜曲率和眼尺寸的影响。
与对侧眼相比,8周的FDM使受试眼出现了-2.70±0.87 D(n = 20)的近视性偏移。近视的主要结构相关因素似乎分别是玻璃体腔延长(0.7±0.3 mm,n = 20)和眼轴延长(0.9±0.3 mm,n = 20)。重复玻璃体内注射DA完全预防了因眼睑缝合导致的近视性偏移(-0.06±0.37 D)、玻璃体腔延长(0.1±0.3 mm,n = 16)和眼轴延长(0.3±0.2 mm,n = 16),而注射生理盐水的效果轻微。
通过缝合眼睑进行形觉剥夺是在兔中诱导显著近视性偏移、玻璃体腔和眼轴延长的有效技术,可作为近视发展的模型。玻璃体内注射DA可延缓与形觉剥夺相关的这些变化。