Nitric oxide synthase regulation and diversity: Implications in Parkinson's disease

被引:90
作者
Kavya, Ramkumar
Saluja, Rohit
Singh, Sarika
Dikshit, Madhu [1 ]
机构
[1] Cent Drug Res Inst, Div Pharmacol, Lucknow 226001, Uttar Pradesh, India
[2] Birla Inst Technol & Sci, Pharm Grp, Pilani 333031, Rajasthan, India
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2006年 / 15卷 / 04期
关键词
nNOS phosphorylation; nNOS spliced variants; iNOS alternate splicing; Parkinson's disease; nNOS; eNOS; NOS polymorphisms; apoptosis;
D O I
10.1016/j.niox.2006.07.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nitric oxide (NO) is a janus faced chemical messenger, which, in the recent years, has been the focus of neurobiologists for its involvement in neurodegenerative disorders in particular, Parkinson's disease (PD). Nitric oxide synthase, the key enzyme involved in NO production exists in three known isoforms. The neuronal and inducible isoforms have been implicated in the pathogenesis of PD. These enzymes are subject to complex expressional and functional regulation involving mRNA diversity, phosphorylation and protein interaction. In the recent years, mRNA diversity and polymorphisms have been identified in the NOS isoforms. Some of these genetic variations have been associated with PD, indicating an etiological role for the NOS genes. This review mainly focuses on the NOS genes-their differential regulation and genetic heterogeneity, highlighting their significance in the pathobiology of PD. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:280 / 294
页数:15
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