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致痫模型在开发癫痫疾病修饰药物中的应用。

Kindling Models of Epileptogenesis for Developing Disease-Modifying Drugs for Epilepsy.

机构信息

Department of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, Texas.

Institute of Pharmacology and Neurotherapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, Texas.

出版信息

Curr Protoc. 2024 Oct;4(10):e70020. doi: 10.1002/cpz1.70020.

Abstract

Kindling models are widely used animal models to study the pathobiology of epilepsy and epileptogenesis. These models exhibit distinctive features whereby sub-threshold stimuli instigate the initial induction of brief focal seizures. Over time, the severity and duration of these seizures progressively increase, leading to a fully epileptic state, which is marked by consistent development of generalized tonic-clonic seizures. Kindling involves focal stimulation via implanted depth electrodes or repeated administration of chemoconvulsants such as pentylenetetrazol. Comparative analysis of preclinical and clinical findings has confirmed a high predictive validity of fully kindled animals for testing novel antiseizure medications. Thus, kindling models remain an essential component of anticonvulsant drug development programs. This article provides a comprehensive guide to working protocols, testing of therapeutic drugs, outcome parameters, troubleshooting, and data analysis for various electrical and chemical kindling epileptogenesis models for new therapeutic development and optimization. The use of pharmacological agents or genetically modified mice in kindling experiments is valuable, offering insights into the impact of a specific target on various aspects of seizures, including thresholds, initiation, spread, termination, and the generation of a hyperexcitable network. These kindling epileptogenesis paradigms are helpful in identifying mechanisms and disease-modifying interventions for epilepsy. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Hippocampal kindling Basic Protocol 2: Amygdala kindling Basic Protocol 3: Rapid hippocampal kindling Basic Protocol 4: Chemical kindling.

摘要

点燃模型是广泛用于研究癫痫病理生理学和癫痫发生的动物模型。这些模型具有独特的特征,即阈下刺激引发短暂局灶性癫痫发作的初始诱导。随着时间的推移,这些癫痫发作的严重程度和持续时间逐渐增加,导致完全癫痫状态,其特征是持续发生全身性强直阵挛性癫痫发作。点燃涉及通过植入的深部电极进行局灶刺激或反复给予化学致惊厥剂,如戊四氮。临床前和临床发现的比较分析证实,完全点燃的动物对测试新型抗癫痫药物具有高度预测有效性。因此,点燃模型仍然是抗惊厥药物开发计划的重要组成部分。本文提供了全面的工作方案指南,用于测试各种电和化学点燃癫痫发生模型的治疗药物、结果参数、故障排除和数据分析,以促进新的治疗方法的开发和优化。在点燃实验中使用药理学药物或基因修饰小鼠是有价值的,它可以深入了解特定靶标对发作的各个方面的影响,包括阈值、起始、传播、终止和兴奋性网络的产生。这些点燃癫痫发生范式有助于确定癫痫的机制和疾病修饰干预措施。© 2024 作者。 Wiley Periodicals LLC 出版的《当代协议》 Basic Protocol 1:海马点燃 Basic Protocol 2:杏仁核点燃 Basic Protocol 3:快速海马点燃 Basic Protocol 4:化学点燃。

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