Peripheral nesfatin-1 reduces basal brain activity but has limited effect on epilepsy-like conditions.

IF 1.3 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY General physiology and biophysics Pub Date : 2024-09-01 DOI:10.4149/gpb_2024026
Ömer Faruk Kalkan, Osman Aktaş, Zafer Şahin, Selcen Aydin Abidin, Abdulhamit Yildirim, Ali Faruk Özyaşar, İbrahim Uzun, İsmail Abidin
{"title":"Peripheral nesfatin-1 reduces basal brain activity but has limited effect on epilepsy-like conditions.","authors":"Ömer Faruk Kalkan, Osman Aktaş, Zafer Şahin, Selcen Aydin Abidin, Abdulhamit Yildirim, Ali Faruk Özyaşar, İbrahim Uzun, İsmail Abidin","doi":"10.4149/gpb_2024026","DOIUrl":null,"url":null,"abstract":"<p><p>In this study, we investigated the effects of peripheral nesfatin-1 on basal brain activity and 4-aminopyridine (4-AP)-induced epileptiform activity, and its relationship with the electrocorticogram (ECoG) power spectrum and EEG bands. Forty-nine male Wistar rats were divided into seven groups: control sham, 4-AP (2.5 mg/kg i.p.), Nesfatin-1 (1, 2, and 4 μg/kg i.p.), Nesfatin-1 (2 μg/kg) post-treatment, and Nesfatin-1 (2 μg/kg) pre-treatment. Recordings were conducted for 70 min under ketamine/xylazine (90/10 mg/kg) anesthesia. In the post-treatment group, nesfatin-1 was injected 20 min after 4-AP induction. In the pre-treatment groups, nesfatin-1 was administered following basal recordings and before 4-AP injection. 4-AP induced epileptiform activity in all animals, peaking at 30 min. Nesfatin-1 (2 μg/kg) reduced basal brain activity (p < 0.05) and decreased alpha, delta, and theta bands in ECoG. Post-treatment of nesfatin-1 did not affect 4-AP-induced activity (p > 0.05) but increased gamma band activity (p > 0.05). Pre-treatment of nesfatin-1 reduced epileptiform activity between 50 and 60 min (p < 0.05), decreased delta bands, and increased gamma bands (p > 0.05). We conclude that peripheral nesfatin-1 modulates normal brain activity but has limited effects on abnormal discharges.</p>","PeriodicalId":12514,"journal":{"name":"General physiology and biophysics","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"General physiology and biophysics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.4149/gpb_2024026","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, we investigated the effects of peripheral nesfatin-1 on basal brain activity and 4-aminopyridine (4-AP)-induced epileptiform activity, and its relationship with the electrocorticogram (ECoG) power spectrum and EEG bands. Forty-nine male Wistar rats were divided into seven groups: control sham, 4-AP (2.5 mg/kg i.p.), Nesfatin-1 (1, 2, and 4 μg/kg i.p.), Nesfatin-1 (2 μg/kg) post-treatment, and Nesfatin-1 (2 μg/kg) pre-treatment. Recordings were conducted for 70 min under ketamine/xylazine (90/10 mg/kg) anesthesia. In the post-treatment group, nesfatin-1 was injected 20 min after 4-AP induction. In the pre-treatment groups, nesfatin-1 was administered following basal recordings and before 4-AP injection. 4-AP induced epileptiform activity in all animals, peaking at 30 min. Nesfatin-1 (2 μg/kg) reduced basal brain activity (p < 0.05) and decreased alpha, delta, and theta bands in ECoG. Post-treatment of nesfatin-1 did not affect 4-AP-induced activity (p > 0.05) but increased gamma band activity (p > 0.05). Pre-treatment of nesfatin-1 reduced epileptiform activity between 50 and 60 min (p < 0.05), decreased delta bands, and increased gamma bands (p > 0.05). We conclude that peripheral nesfatin-1 modulates normal brain activity but has limited effects on abnormal discharges.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
外周 nesfatin-1 可降低大脑的基础活动,但对癫痫样病症的影响有限。
本研究探讨了外周奈司法汀-1对基础脑活动和4-氨基吡啶(4-AP)诱导的癫痫样活动的影响,以及其与皮层电图(ECoG)功率谱和脑电图波段的关系。49 只雄性 Wistar 大鼠被分为 7 组:假对照组、4-AP(2.5 毫克/千克静注)组、Nesfatin-1(1、2 和 4 微克/千克静注)组、Nesfatin-1(2 微克/千克)后处理组和 Nesfatin-1 (2 微克/千克)前处理组。在氯胺酮/氯丙嗪(90/10 毫克/千克)麻醉下进行了 70 分钟的记录。后处理组在 4-AP 诱导 20 分钟后注射奈司他丁-1。在预处理组中,在基础记录后和注射4-AP前注射内司法汀-1。4-AP 可诱导所有动物出现癫痫样活动,并在 30 分钟时达到高峰。奈斯法丁-1(2 μg/kg)可降低基础脑活动(p < 0.05),并减少心电图中的α、δ和θ波段。后处理奈司他丁-1 不会影响 4-AP 诱导的活动(p > 0.05),但会增加伽马波段的活动(p > 0.05)。预处理奈司他丁-1可减少50至60分钟的癫痫样活动(p < 0.05),减少δ波段,增加γ波段(p > 0.05)。我们的结论是,外周奈司法汀-1能调节正常的大脑活动,但对异常放电的影响有限。
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 去求助
来源期刊
General physiology and biophysics
General physiology and biophysics 生物-生化与分子生物学
CiteScore
2.70
自引率
0.00%
发文量
42
审稿时长
6-12 weeks
期刊介绍: General Physiology and Biophysics is devoted to the publication of original research papers concerned with general physiology, biophysics and biochemistry at the cellular and molecular level and is published quarterly by the Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences.
期刊最新文献
Bioinformatics analysis of potential ferroptosis and non-alcoholic fatty liver disease biomarkers. Bioinformatics screening and verification of ischemic stroke-related key genes and drug prediction. Cytotoxic and pro-oxidant profile of a photosensitive ruthenium nitrosyl candidate for NO delivery in healthy human fibroblasts. LncRNA SNHG1 knockdown attenuates lipopolysaccharide-induced acute lung injury via regulating miR199a-3p/ROCK2 axis. Peripheral nesfatin-1 reduces basal brain activity but has limited effect on epilepsy-like conditions.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1