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使用戊四氮诱导的癫痫模型评估卡瓦水提取物对斑马鱼的抗惊厥特性。

Evaluation of Anti-Convulsive Properties of Aqueous Kava Extract on Zebrafish Using the PTZ-Induced Seizure Model.

作者信息

Jaiswal Yogini, Shaikh Mohd Farooq, Wang Ilya, Yong Yanning, Lin Lin Lee Vanessa, Williams Leonard

机构信息

Center for Excellence in Post-Harvest Technologies, The North Carolina Research Campus, 500 Laureate Way, Kannapolis, NC 28081, USA.

Neuropharmacology Research Laboratory, Jeffrey Cheah School of Medicine & Health Sciences, Monash University Malaysia, Bandar Sunway 47500, Malaysia.

出版信息

Brain Sci. 2020 Aug 11;10(8):541. doi: 10.3390/brainsci10080541.

DOI:10.3390/brainsci10080541
PMID:32796575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7463627/
Abstract

Kava roots have been extensively studied in clinical trials as potential candidate anti-anxiety drugs. However, anti-convulsive properties of various tissues of stems of Kava have not been reported to date. The objective of the study was to evaluate the anti-convulsive potential of aqueous extracts prepared from specific tissues of Kava () stems in zebrafish, using the PTZ-induced seizure model. The potency of each extract was compared in terms of the intensity of seizure scores and onset time after pre-treating the zebrafish before the PTZ challenge. The results indicate that aqueous extract of Kava stems without peel after 45 min of pre-treatment exhibited anti-convulsive potential at the dose of 50 mg/L. This study provides evidence to the anti-convulsive properties of peeled Kava stems and its potential for investigation and design of candidate anti-convulsive drugs.

摘要

卡瓦根已在临床试验中作为潜在的抗焦虑药物候选物进行了广泛研究。然而,迄今为止,尚未有关于卡瓦茎不同组织抗惊厥特性的报道。本研究的目的是使用戊四氮诱导的癫痫模型,评估从卡瓦()茎的特定组织制备的水提取物在斑马鱼中的抗惊厥潜力。在戊四氮激发前对斑马鱼进行预处理后,根据癫痫发作评分的强度和发作时间比较每种提取物的效力。结果表明,预处理45分钟后无外皮的卡瓦茎水提取物在50 mg/L的剂量下表现出抗惊厥潜力。本研究为去皮卡瓦茎的抗惊厥特性及其作为候选抗惊厥药物的研究和设计潜力提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/06917e976d60/brainsci-10-00541-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/7e0570b83745/brainsci-10-00541-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/ad0a224e60b4/brainsci-10-00541-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/88390ca5d9e5/brainsci-10-00541-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/d79e25dcb8cd/brainsci-10-00541-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/75a9f9524bfe/brainsci-10-00541-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/33feae42e8df/brainsci-10-00541-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/06917e976d60/brainsci-10-00541-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/7e0570b83745/brainsci-10-00541-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/ad0a224e60b4/brainsci-10-00541-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/88390ca5d9e5/brainsci-10-00541-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/d79e25dcb8cd/brainsci-10-00541-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/75a9f9524bfe/brainsci-10-00541-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/33feae42e8df/brainsci-10-00541-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be7/7463627/06917e976d60/brainsci-10-00541-g007.jpg

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本文引用的文献

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Front Pharmacol. 2018 Feb 23;9:139. doi: 10.3389/fphar.2018.00139. eCollection 2018.
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Zebrafish as a Model for Epilepsy-Induced Cognitive Dysfunction: A Pharmacological, Biochemical and Behavioral Approach.斑马鱼作为癫痫诱发认知功能障碍的模型:药理学、生物化学及行为学方法
Front Pharmacol. 2017 Aug 3;8:515. doi: 10.3389/fphar.2017.00515. eCollection 2017.
3
Garcinol Upregulates GABAA and GAD65 Expression, Modulates BDNF-TrkB Pathway to Reduce Seizures in Pentylenetetrazole (PTZ)-Induced Epilepsy.
藤黄脂上调GABAA和GAD65表达,调节BDNF-TrkB通路以减少戊四氮(PTZ)诱导的癫痫发作。
Med Sci Monit. 2016 Nov 17;22:4415-4425. doi: 10.12659/msm.897579.
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Kavain, the Major Constituent of the Anxiolytic Kava Extract, Potentiates GABAA Receptors: Functional Characteristics and Molecular Mechanism.卡瓦因,抗焦虑卡瓦提取物的主要成分,增强GABAA受体:功能特性及分子机制
PLoS One. 2016 Jun 22;11(6):e0157700. doi: 10.1371/journal.pone.0157700. eCollection 2016.
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The pattern of c-Fos expression and its refractory period in the brain of rats and monkeys.大鼠和猴脑中 c-Fos 表达的模式及其不应期。
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