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哺乳动物半胱氨酸蛋白酶抑制剂及其在脑部疾病中的作用

Mammalian cystatin and protagonists in brain diseases.

机构信息

Department of Zoology, Faculty of Life Sciences, Aligarh Muslim University, Aligarh, India.

Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.

出版信息

J Biomol Struct Dyn. 2020 Apr;38(7):2171-2196. doi: 10.1080/07391102.2019.1620636. Epub 2019 Jun 5.

Abstract

Cystatins are the thiol Proteinase inhibitors, present ubiquitously in mammalian body. They prevent unwanted proteolysis and play important role in several diseases. Regulation of cysteine Proteinase and their inhibitors is of utmost importance in neurodegenerative diseases like Alzheimer, amyloid angiopathy and in many other diseases. The action of these cysteine proteases is biologically controlled by proteinase inhibitors namely cystatins(cys) they constitute a superfamily of homologous proteins. The major role of cystatins is to protect the organism against endogenous proteases released from lysosomes, invading microorganisms and parasites that use cysteine proteases to enter the body. An enormous progress has been made in understanding of protein degradation process under normal and pathological conditions; in fact proteases are now clearly viewed as important drug targets. Some studies have suggested that cystatin C is a target for intervention in neurological disorders because its expression increases in response to human neurological disorders and in animal models of neurodegenerative states. Although, these studies did not clarify whether CysC up-regulation is a pathogenic factor in neurodegenerative disorders or whether it represents a neuroprotective compensatory response of the organisms aimed to prevent progression of the disease. However, for other diseases in some cases cystatins other than cys C are up regulated and in some it is down regulated.Cystatins have been implicated in the processes of neuronal degeneration and repair of the nervous system. Both CysC and CysB are potent, reversible inhibitors of most of the currently known cathepsins. The extent of proteolytic activity at any given time and location is the result of a balance between active proteases and physiological inhibitors. Uncontrolled proteolysis as a result of imbalance between active proteases and their endogenous inhibitors has been associated with neuronal cell death in different neuronal diseases, including brain tumors, stroke, some forms of epilepsy, Alzheimer's disease, and neurological autoimmune diseases.An antidepressant is a psychiatric medication used to alleviate mood disorders, major depression and other brain diseases. Drugs including the monoamine oxidase inhibitors (MAOIs), tricyclic antidepressants (TCAs), and serotonin-norepinephrine reuptake inhibitors (SNRIs) are most commonly used antidepressant. They are also used to treat other conditions, such as anxiety disorders, obsessive compulsive disorder, eating disorders, and chronic pain. Although the mechanisms of the action of these antidepressants are not precisely understood, their principal target of action is at the monoamine transporter proteins located at nerve endings. Monoamine neurotransmitter transporters act to terminate synaptic neurotransmission. Selective serotonin reuptake inhibitors or SSRIs are also most widely used class of antidepressants. They work by increasing the level of serotonin in the brain. SSRIs have fewer and milder side effects, fewer drug interactions, and are much less likely to be associated with suicide than TCAs.These antidepressants shows binding when incubated with cystatin, presenting the involvement of these antidepressant in cascade of disease, as leaving no cystatin to inhibit the cathepsin showing the myriad side effect after the administration of antidepressant. This might be one of the reason in the mechanism of action of antidepressant.So this review expound about the role of cystatins in neurological diseases which is considered to be highly significant as it pave the way for commanding tool in the drug design.Communicated by Ramaswamy H. Sarma.

摘要

组织蛋白酶抑制剂是一种存在于哺乳动物体内的硫醇蛋白酶抑制剂。它们可以防止不受控制的蛋白水解,并在许多疾病中发挥重要作用。调节半胱氨酸蛋白酶及其抑制剂在阿尔茨海默病、淀粉样血管病等神经退行性疾病以及许多其他疾病中非常重要。这些半胱氨酸蛋白酶的作用通过蛋白酶抑制剂(即胱抑素)来进行生物控制,它们构成了同源蛋白的超家族。胱抑素的主要作用是防止内源性蛋白酶从溶酶体中释放出来,防止入侵的微生物和寄生虫利用半胱氨酸蛋白酶进入体内。在理解正常和病理条件下的蛋白降解过程方面已经取得了巨大进展;事实上,蛋白酶现在被明确视为重要的药物靶点。一些研究表明,胱抑素 C 是干预神经紊乱的靶点,因为它的表达在人类神经紊乱和神经退行性状态的动物模型中增加。尽管这些研究并没有阐明胱抑素 C 的上调是否是神经退行性疾病的致病因素,或者它是否代表了生物体的一种神经保护代偿反应,旨在防止疾病的进展。然而,对于其他疾病,在某些情况下,除了胱抑素 C 之外,其他胱抑素也会上调,而在某些情况下则会下调。胱抑素参与神经元变性和神经系统修复的过程。CysC 和 CysB 都是目前已知的大多数组织蛋白酶的有效、可逆抑制剂。在任何给定时间和位置的蛋白水解活性的程度是活性蛋白酶和生理抑制剂之间平衡的结果。由于活性蛋白酶和其内源性抑制剂之间的失衡导致的不受控制的蛋白水解与不同神经元疾病中的神经元细胞死亡有关,包括脑肿瘤、中风、某些形式的癫痫、阿尔茨海默病和神经自身免疫性疾病。抗抑郁药是一种用于缓解情绪障碍、重度抑郁症和其他脑部疾病的精神药物。包括单胺氧化酶抑制剂 (MAOIs)、三环抗抑郁药 (TCAs) 和 5-羟色胺去甲肾上腺素再摄取抑制剂 (SNRIs) 在内的药物是最常用的抗抑郁药。它们还用于治疗其他疾病,如焦虑症、强迫症、饮食失调和慢性疼痛。尽管这些抗抑郁药的作用机制尚不完全清楚,但它们的主要作用靶点是位于神经末梢的单胺转运蛋白。单胺神经递质转运蛋白作用于终止突触神经传递。选择性 5-羟色胺再摄取抑制剂或 SSRI 也是最广泛使用的抗抑郁药类别。它们通过增加大脑中的 5-羟色胺水平起作用。SSRIs 的副作用更少且更温和,药物相互作用更少,与 TCA 相比,与自杀的关联要小得多。这些抗抑郁药在与胱抑素孵育时表现出结合,表明这些抗抑郁药参与了疾病级联反应,因为没有胱抑素来抑制组织蛋白酶,在服用抗抑郁药后表现出了无数的副作用。这可能是抗抑郁药作用机制之一。因此,本综述阐述了胱抑素在神经退行性疾病中的作用,这被认为是非常重要的,因为它为药物设计提供了一个指挥工具。由 Ramaswamy H. Sarma 交流。

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