Effects of unilateral topical atropine on binocular pupil responses and eye growth in mice

被引:17
作者
Barathi, V. A. [1 ,2 ]
Beuerman, Roger W. [2 ,3 ]
Schaeffel, Frank [1 ]
机构
[1] Univ Eye Hosp Tubingen, Ctr Ophthalmol, Ophthalm Res Ctr, Sect Neurobiol Eye, D-72076 Tubingen, Germany
[2] Singapore Eye Res Inst, Singapore 168751, Singapore
[3] Natl Univ Singapore, Natl Univ Hosp, Yong Loo Lin Sch Med, Dept Ophthalmol, Singapore 119074, Singapore
关键词
Pupillary response; Atropine; Interocular comparisons; Mouse; Axial length; Refraction; Myopia; EXPERIMENTAL MYOPIA; RECEPTOR ANTAGONISTS; MOUSE EYE; CHILDREN; PROGRESSION; EFFICACY; MONKEYS; CHICK; MODEL;
D O I
10.1016/j.visres.2008.11.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Purpose: Studies on drugs selected to target myopia development often use the vehicle-treated fellow eye as a control. However, it is not clear how much of the drug reaches the fellow eye, rendering it a potentially invalid control. Therefore, in this study, pupil responses were used to probe the effects of atropine in both eyes in mice, after unilateral topical application. In a second experiment, interocular differences in refractive development and axial eye growth were studied while atropine was applied daily to one eye. Methods: In 20 C57BL/6 (B6) wildtype mice, a single drop of 1% atropine solution was instilled into one eye. Mice were gently restrained by holding their necks while video image processing software detected the pupil and measured its diameter at a sampling rate of 30 Hz. A bright green LED, attached to the photoretinoscope of the video camera, was flashed. Pupil responses were quantified daily over a period of 2 weeks. In another group of 24 mice, one drop of 1% atropine was applied daily for 28 days. Axial length was measured pre- and post-treatment, using low coherence interferometry (the Zeiss AC-Master). Refractive development was measured by infrared photorefraction. Results: Similar to previous findings with the same device, untreated eyes displayed a pupil constriction of 24.84 +/- 1.73% upon stimulation with the green LED. A single drop of 1% atropine caused complete suppression with no significant recovery over the whole observation period of two weeks. The responses in the fellow eye were temporarily reduced to about 75% and then recovered towards baseline. After daily atropine application, there was significant reduction in axial length of the eyes, relative to the saline-treated fellow eyes (3.234 +/- 0.186 versus 3.378 +/- 0.176 mm, n = 24, p < 0.01, paired t-test) and the refractions became more hyperopic/less myopic (+13.46 +/- 2.15 D versus +10.06 +/- 2.02 D, n = 24, p < 0.01). Conclusions: In line with previous findings, one drop of atropine solution caused a long lasting suppression of pupil responses in the mouse eye. New data show that the transfer to the fellow eye was limited, making interocular comparisons feasible. It is also new that topical atropine reduced axial eye growth even when mice had largely normal vision. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:383 / 387
页数:5
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