Suppr超能文献

开发用于治疗神经系统疾病的KCC2疗法。

Development of KCC2 therapeutics to treat neurological disorders.

作者信息

Kadam Shilpa D, Hegarty Shane V

机构信息

Axonis Therapeutics Inc., Boston, MA, United States.

出版信息

Front Mol Neurosci. 2024 Dec 10;17:1503070. doi: 10.3389/fnmol.2024.1503070. eCollection 2024.

Abstract

KCC2 is CNS neuron-specific chloride extruder, essential for the establishment and maintenance of the transmembrane chloride gradient, thereby enabling synaptic inhibition within the CNS. Herein, we highlight KCC2 hypofunction as a fundamental and conserved pathology contributing to neuronal circuit excitation/inhibition (E/I) imbalances that underly epilepsies, chronic pain, neuro-developmental/-traumatic/-degenerative/-psychiatric disorders. Indeed, downstream of both acquired and genetic factors, multiple pathologies (e.g., hyperexcitability and inflammation) converge to impair KCC2-dependent inhibition in CNS. When KCC2 hypofunction occurs, affected neurons are disinhibited due to impaired inhibitory responses to GABA/glycine. This causes neuronal hyperexcitability, disinhibition within neuron circuits, and disrupted neurological functions. More recently, KCC2 was identified as a genetically-validated target for epilepsy, intellectual disability, and autism spectrum disorder, and pathogenic mutations in human SLC12A5 gene were linked to psychiatric/mood disorders. The broad therapeutic utility of KCC2-upmodulating drugs relates to its critical role in determining inhibitory activity of GABAergic neurotransmission, a mechanism widely targeted by several drugs. However, in cases of KCC2 hypofunction GABAergic neurotransmission can be depolarizing/excitatory, thereby impairing endogenous neuronal inhibition while also limiting the effectiveness of existing therapeutics targeting/requiring GABAergic pathway inhibition. Several preclinical reports have shown that KCC2 upmodulating treatments rescue and increase the efficacy of anti-seizure and analgesic medications. Thus, a first-in-class KCC2-potentiating therapy would provide a novel mechanism for restoring physiological CNS inhibition and addressing drug resistance in patients with E/I imbalance pathologies. Herein, we discuss progress toward and further work needed to develop the first-in-class KCC2 therapeutics to treat neurological disorder patients.

摘要

KCC2是中枢神经系统(CNS)神经元特异性的氯离子转运体,对于跨膜氯离子梯度的建立和维持至关重要,从而使中枢神经系统内能够产生突触抑制。在此,我们强调KCC2功能减退是一种基本且保守的病理状态,它会导致神经元回路兴奋/抑制(E/I)失衡,而这种失衡是癫痫、慢性疼痛、神经发育/创伤/退行性/精神疾病的基础。事实上,在获得性和遗传因素的下游,多种病理状态(如兴奋性过高和炎症)都会导致中枢神经系统中依赖KCC2的抑制作用受损。当KCC2功能减退时,受影响的神经元会因对γ-氨基丁酸(GABA)/甘氨酸的抑制反应受损而解除抑制。这会导致神经元兴奋性过高、神经元回路内的去抑制以及神经功能紊乱。最近,KCC2被确定为癫痫、智力残疾和自闭症谱系障碍的经基因验证的靶点,人类SLC12A5基因的致病突变与精神/情绪障碍有关。上调KCC2的药物具有广泛的治疗用途,这与其在决定GABA能神经传递抑制活性方面的关键作用有关,而这一机制是多种药物广泛靶向的。然而,在KCC2功能减退的情况下,GABA能神经传递可能会去极化/兴奋,从而损害内源性神经元抑制,同时也限制了现有针对/需要抑制GABA能通路的治疗方法的有效性。多项临床前报告表明,上调KCC2的治疗方法可挽救并提高抗癫痫和止痛药物的疗效。因此,首个一流的KCC2增强疗法将为恢复生理性中枢神经系统抑制以及解决E/I失衡病理患者的耐药性提供一种新机制。在此,我们讨论开发首个一流的KCC2疗法以治疗神经疾病患者的进展以及所需的进一步工作。

相似文献

1
Development of KCC2 therapeutics to treat neurological disorders.开发用于治疗神经系统疾病的KCC2疗法。
Front Mol Neurosci. 2024 Dec 10;17:1503070. doi: 10.3389/fnmol.2024.1503070. eCollection 2024.

本文引用的文献

9
Therapeutic potential for KCC2-targeted neurological diseases.针对KCC2的神经系统疾病的治疗潜力。
Jpn Dent Sci Rev. 2023 Dec;59:431-438. doi: 10.1016/j.jdsr.2023.11.001. Epub 2023 Nov 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验