Involvement of neuronal nitric oxide synthase in N-methyl-N-nitrosourea-induced retinal degeneration in mice

被引:4
作者
Koriyama, Yoshiki [1 ,2 ]
Hisano, Suguru [3 ]
Ogai, Kazuhiro [4 ]
Sugitani, Kayo [5 ]
Furukawa, Ayako [1 ,2 ]
Kato, Satoru [3 ]
机构
[1] Suzuka Univ Med Sci, Grad Sch, Suzuka 5138670, Japan
[2] Suzuka Univ Med Sci, Fac Pharmaceut Sci, Suzuka 5138670, Japan
[3] Kanazawa Univ, Grad Sch Med, Dept Mol Neurobiol, Kanazawa, Ishikawa, Japan
[4] Kanazawa Univ, Inst Med Pharmaceut & Hlth Sci, Wellness Promot Sci Ctr, Kanazawa, Ishikawa, Japan
[5] Kanazawa Univ, Grad Sch Med, Div Hlth Sci, Kanazawa, Ishikawa, Japan
关键词
Neurotoxicity; Nitric oxide; Retina; PHOTORECEPTOR CELL-DEATH; ANIMAL-MODELS; MECHANISMS; CYCLASE;
D O I
10.1016/j.jphs.2015.02.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
N-methyl-N-nitrosourea (MNU) is widely used to study the mechanism of retinal degenerative diseases (RDs) because of its selectivity of photoreceptor cell death. Many reports suggest that excessive nitric oxide (NO) plays a crucial role in neuronal cell death. We hypothesized that nitric oxide synthase (NOS)/NO are involved in photoreceptor cell death by MNU. We found that the levels of NO increased after MNU treatment. Furthermore, we demonstrated that neuronal NOS specific inhibitor attenuated photoreceptor cell death by MNU in mice. We believe that our findings might be a new target for the treatment of RDs. (C) 2015 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:394 / 396
页数:3
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