Oral diazepam suppresses pentylenetetrazole-induced seizure-like behavior in adult zebrafish: A tool for nonclinical studies

Q2 Pharmacology, Toxicology and Pharmaceutics
Arlindo César Matias Pereira, Arthur Arantes da Cunha, H. Carvalho, I. Ferreira, J. C. T. Carvalho
{"title":"Oral diazepam suppresses pentylenetetrazole-induced seizure-like behavior in adult zebrafish: A tool for nonclinical studies","authors":"Arlindo César Matias Pereira, Arthur Arantes da Cunha, H. Carvalho, I. Ferreira, J. C. T. Carvalho","doi":"10.7324/japs.2023.133132","DOIUrl":null,"url":null,"abstract":"Epilepsy is one of the most severe and common neurologic disorders, affecting more than 50 million people worldwide. This disturbance is characterized by spontaneous and recurrent convulsions due to abnormal, excessive, and synchronous electrical triggers in the neural network. This study aimed to describe the behavior analysis of epileptic behavior in adult zebrafish induced by intraperitoneal (ip) pentylenetetrazole (PTZ) and the effects of oral (po) diazepam (DZP) on it. Animals’ behavior was recorded for 20 minutes after treatment with saline solution (vehicle), PTZ (125/250/400/500 mg/kg), or cotreatment with DZP (10 mg/kg) + PTZ (250/400 mg/kg). Then, altered behavioral manifestation was scored between 0 and 6 according to the following parameters: seizure score and cumulative frequency, seizure intensity measured through the area under the curve, clonic seizure latency, tonic seizure latency, and survival rate. The control group had scores between 0 and 3 and smaller convulsion intensity when compared to the PTZ-treated group. This latter group’s scores ranged from 0 to 6. Moreover, the convulsion intensity ranged from the median (PTZ at 125 mg/kg) to high (PTZ at 250/400/500 mg/kg). The latency to score 4 was similar in all PTZ treatments. However, latency to score 5 was higher in groups treated with PTZ at 400 and 500 mg/kg and was not detected in the group treated with PTZ at 125 mg/kg. Cotreatment with DZP + PTZ had scores between 0 and 5, less convulsion intensity, and higher latency to scores 4 and 5. Animals’ death occurred only in the group treated with PTZ at 500 mg/kg. These results show behavioral characterization of seizure scores in zebrafish treated with PTZ (ip) and DZP (po). This is a valuable tool for translational research and a more feasible model to replicate data in mammals.","PeriodicalId":15126,"journal":{"name":"journal of applied pharmaceutical science","volume":"373 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"journal of applied pharmaceutical science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7324/japs.2023.133132","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

Abstract

Epilepsy is one of the most severe and common neurologic disorders, affecting more than 50 million people worldwide. This disturbance is characterized by spontaneous and recurrent convulsions due to abnormal, excessive, and synchronous electrical triggers in the neural network. This study aimed to describe the behavior analysis of epileptic behavior in adult zebrafish induced by intraperitoneal (ip) pentylenetetrazole (PTZ) and the effects of oral (po) diazepam (DZP) on it. Animals’ behavior was recorded for 20 minutes after treatment with saline solution (vehicle), PTZ (125/250/400/500 mg/kg), or cotreatment with DZP (10 mg/kg) + PTZ (250/400 mg/kg). Then, altered behavioral manifestation was scored between 0 and 6 according to the following parameters: seizure score and cumulative frequency, seizure intensity measured through the area under the curve, clonic seizure latency, tonic seizure latency, and survival rate. The control group had scores between 0 and 3 and smaller convulsion intensity when compared to the PTZ-treated group. This latter group’s scores ranged from 0 to 6. Moreover, the convulsion intensity ranged from the median (PTZ at 125 mg/kg) to high (PTZ at 250/400/500 mg/kg). The latency to score 4 was similar in all PTZ treatments. However, latency to score 5 was higher in groups treated with PTZ at 400 and 500 mg/kg and was not detected in the group treated with PTZ at 125 mg/kg. Cotreatment with DZP + PTZ had scores between 0 and 5, less convulsion intensity, and higher latency to scores 4 and 5. Animals’ death occurred only in the group treated with PTZ at 500 mg/kg. These results show behavioral characterization of seizure scores in zebrafish treated with PTZ (ip) and DZP (po). This is a valuable tool for translational research and a more feasible model to replicate data in mammals.
口服地西泮抑制成年斑马鱼戊四唑诱导的癫痫样行为:非临床研究的工具
癫痫是最严重和最常见的神经系统疾病之一,影响着全世界5000多万人。这种障碍的特征是由于神经网络中异常、过度和同步的电触发而引起的自发和反复的抽搐。本研究旨在描述腹腔注射戊四唑(PTZ)诱导成年斑马鱼癫痫行为的行为分析及口服地西泮(DZP)对其的影响。用生理盐水(载药)、PTZ (125/250/400/500 mg/kg)或DZP (10 mg/kg) + PTZ (250/400 mg/kg)共治疗20分钟,记录动物行为。然后根据癫痫发作评分和累积频率、曲线下面积测量的癫痫发作强度、阵挛性癫痫发作潜伏期、强直性癫痫发作潜伏期、存活率等参数对行为改变表现进行评分,评分范围为0 ~ 6分。与ptz治疗组相比,对照组的评分在0到3分之间,惊厥强度较小。后一组的得分从0到6不等。此外,痉挛强度从中位(PTZ为125 mg/kg)到高(PTZ为250/400/500 mg/kg)不等。到4分的潜伏期在所有PTZ治疗中相似。然而,PTZ剂量为400和500 mg/kg组的潜伏期高于PTZ剂量为125 mg/kg组。DZP + PTZ联合治疗的评分在0 ~ 5分之间,惊厥强度较小,潜伏期较高,评分为4 ~ 5分。PTZ剂量为500mg /kg组出现动物死亡。这些结果显示了PTZ (ip)和DZP (po)治疗的斑马鱼癫痫发作评分的行为特征。这是一种有价值的转化研究工具,也是一种在哺乳动物中复制数据的更可行的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
journal of applied pharmaceutical science
journal of applied pharmaceutical science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.20
自引率
0.00%
发文量
224
期刊介绍: Journal of Applied Pharmaceutical Science (JAPS) is a monthly, international, open access, journal dedicated to various disciplines of pharmaceutical and allied sciences. JAPS publishes manuscripts (Original research and review articles Mini-reviews, Short communication) on original work, either experimental or theoretical in the following areas; Pharmaceutics & Biopharmaceutics Novel & Targeted Drug Delivery Nanotechnology & Nanomedicine Pharmaceutical Chemistry Pharmacognosy & Ethnobotany Phytochemistry Pharmacology & Toxicology Pharmaceutical Biotechnology & Microbiology Pharmacy practice & Hospital Pharmacy Pharmacogenomics Pharmacovigilance Natural Product Research Drug Regulatory Affairs Case Study & Full clinical trials Biomaterials & Bioactive polymers Analytical Chemistry Physical Pharmacy.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信