Emerging roles of system [Formula: see text] antiporter and its inhibition in CNS disorders.

Q3 Biochemistry, Genetics and Molecular Biology Molecular Membrane Biology Pub Date : 2015-01-01 DOI:10.3109/09687688.2015.1096972
Dhaval Patel, Prashant S Kharkar, Mukesh Nandave
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引用次数: 11

Abstract

System [Formula: see text] is an antiporter belonging to the hetero(di)meric amino acid transporter family. It is located on astrocytes as well as on blood-brain barrier within the CNS. It plays a pivotal role in free radical neutralization as well as neuronal signalling by regulating the glutathione production which occurs via the exchange of intracellular glutamate with extracellular cystine at 1:1 molar ratio. Understandably, it is a vital component responsible for the maintenance of neuronal homeostasis (e.g. redox state). Hence, it could be postulated that any perturbation in system [Formula: see text] function may contribute, directly or indirectly, to the pathophysiology of a variety of CNS disorders like Alzheimer's disease, schizophrenia, drug addiction, depression, multiple sclerosis, hypoglycemic neuronal cell death, glioma, and excitotoxicity, making system [Formula: see text] a promising target for treating CNS disorders. In recent times, recognizing the potential of this target, variety of inhibitors has been synthesized by modifying commercially available potent inhibitors including sulfasalazine, erastin, and sorafenib. Although, they have demonstrated efficacy, the in-depth data is still lacking to warrant their use for the treatment of aforementioned CNS disorders. In this review, we discuss the in-depth role of system [Formula: see text] transporter in maintaining normal physiology as well as in the pathophysiology of CNS diseases. Additionally, we have also listed some of the potent inhibitors of system [Formula: see text]. In conclusion, the critical role of system [Formula: see text] in multiple CNS disorders and advanced research on its inhibitors have promising future prospects for better management of the CNS ailments.

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系统的新角色[公式:见文本]逆向转运蛋白及其在中枢神经系统疾病中的抑制作用。
系统[公式:见正文]是一种反转运蛋白,属于异(二)氨基转运蛋白家族。它位于中枢神经系统内星形胶质细胞和血脑屏障上。它在自由基中和和神经元信号传导中起着关键作用,通过调节谷胱甘肽的产生,这是通过细胞内谷氨酸与细胞外胱氨酸以1:1的摩尔比交换发生的。可以理解,它是负责维持神经元稳态(例如氧化还原状态)的重要组成部分。因此,可以假设系统功能中的任何干扰都可能直接或间接地导致各种中枢神经系统疾病的病理生理,如阿尔茨海默病、精神分裂症、药物成瘾、抑郁症、多发性硬化症、低血糖性神经元细胞死亡、胶质瘤和兴奋性毒性,使系统成为治疗中枢神经系统疾病的一个有希望的靶点。近年来,认识到这一靶点的潜力,通过修饰市售的有效抑制剂,合成了各种抑制剂,包括磺胺氮嗪、erastin和索拉非尼。尽管它们已经证明了疗效,但仍缺乏深入的数据来保证它们用于治疗上述中枢神经系统疾病。在这篇综述中,我们深入讨论了系统转运体在维持正常生理以及在中枢神经系统疾病病理生理中的作用。此外,我们还列出了一些有效的系统抑制剂[公式:见文本]。总之,该系统在多种中枢神经系统疾病中的关键作用以及对其抑制剂的深入研究为更好地治疗中枢神经系统疾病提供了良好的前景。
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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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