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Implication of the Kallikrein-Kinin System in Neurological Disorders: Quest for Potential Biomarkers and Mechanisms

机译:激肽释放酶-激肽系统在神经系统疾病中的意义:潜在的生物标志物和机制的追求。

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摘要

Neurological disorders represent major health concerns in terms of comorbidity and mortality worldwide. Despite a tremendous increase in our understanding of the pathophysiological processes involved in disease progression and prevention, the accumulated knowledge so far resulted in relatively moderate translational benefits in terms of therapeutic interventions and enhanced clinical outcomes. Aiming at specific neural molecular pathways, different strategies have been geared to target the development and progression of such disorders. The kallikrein-kinin system (KKS) is among the most delineated candidate systems due to its ubiquitous roles mediating several of the pathophysiological features of these neurological disorders as well as being implicated in regulating various brain functions. Several experimental KKS models revealed that the inhibition or stimulation of the two receptors of the KKS system (B1R and B2R) can exhibit neuroprotective and/or adverse pathological outcomes. This updated review provides background details of the KKS components and their functions in different neurological disorders including temporal lobe epilepsy, traumatic brain injury, stroke, spinal cord injury, Alzheimer’s disease, multiple sclerosis and glioma. Finally, this work will highlight the putative roles of the KKS components as potential neurotherapeutic targets and provide future perspectives on the possibility of translating these findings into potential clinical biomarkers in neurological disease.
机译:就全球合并症和死亡率而言,神经系统疾病代表着主要的健康问题。尽管我们对疾病进展和预防所涉及的病理生理过程的理解有了极大的提高,但迄今为止积累的知识在治疗干预和提高临床疗效方面带来了相对中等的转化益处。针对特定的神经分子途径,已经针对不同疾病的发展和进程采取了不同的策略。激肽释放酶激肽系统(KKS)是最被描述的候选系统之一,因为它的普遍作用是介导这些神经系统疾病的几种病理生理特征,并参与调节各种脑功能。几种实验性KKS模型显示,抑制或刺激KKS系统的两个受体(B1R和B2R)可以表现出神经保护作用和/或不利的病理结果。这份更新后的评论提供了有关KKS成分及其在不同神经系统疾病中的功能的背景细节,包括颞叶癫痫,颅脑外伤,中风,脊髓损伤,阿尔茨海默氏病,多发性硬化症和神经胶质瘤。最后,这项工作将强调KKS成分作为潜在的神经治疗靶点的假定作用,并就将这些发现转化为神经疾病潜在的临床生物标志物的可能性提供未来展望。

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