Refractive development and form-deprivation induced myopic refractive error in CBA/CaJ mice.
- Author:
Yun-Yun LI
1
;
Kang-Wei QIAN
1
;
Xiao-Hua WU
1
;
Wei ZHOU
1
;
Yong-Mei ZHONG
2
;
Shi-Jun WENG
3
Author Information
1. Institute of Neurobiology, Institutes of Brain Science, State Key Laboratory of Medical Neurobiology and Collaborative Innovation Center for Brain Science, Fudan University, Shanghai 200032, China.
2. Institute of Neurobiology, Institutes of Brain Science, State Key Laboratory of Medical Neurobiology and Collaborative Innovation Center for Brain Science, Fudan University, Shanghai 200032, China. ymzhong@fudan.edu.cn.
3. Institute of Neurobiology, Institutes of Brain Science, State Key Laboratory of Medical Neurobiology and Collaborative Innovation Center for Brain Science, Fudan University, Shanghai 200032, China. sjweng@fudan.edu.cn.
- Publication Type:Journal Article
- MeSH:
Animals;
Disease Models, Animal;
Eye;
Mice;
Mice, Inbred C57BL;
Mice, Inbred CBA;
Myopia;
Refraction, Ocular;
Sensory Deprivation
- From:
Acta Physiologica Sinica
2016;68(2):135-140
- CountryChina
- Language:Chinese
-
Abstract:
Due to the advantages in genetic manipulation, mice have become one of the most commonly used mammalian models for the study of mechanisms underlying myopia development. However, the vast majority of laboratory mouse strains are incapable of synthesizing melatonin, a neurohormone that may play an important role in myopia generation in humans. The present study investigated refractive development profiles in the CBA/CaJ mouse, a strain proficient in melatonin, and determined whether and how its refractive development could be affected by form-deprivation. Eccentric infrared photoretinoscopy revealed that this animal could be stably refracted, and the refractive error underwent developmental changes, which increased with age in the hyperopic direction and eventually got stable approximately 9 weeks after birth. The absolute values of refractive error in CBA/CaJ mice were larger than those of age-matched C57BL/6 mice, whereas the time points when refractive error reached steady state were similar between the two strains. Five weeks of form-deprivation applied to 3-week-old CBA/CaJ mice by translucent occluder wear caused a significant myopic shift in refractive error, indicating that this strain could be adequately used as a myopia model.
