The Heterogenous Properties of Potassium Glutamate Neurons in the Ventral and Dorsal Regions of the SA1 Hippopotamus

IF 4.033 Q4 Biochemistry, Genetics and Molecular Biology
A. S. Galashin, M. V. Konakov, V. V. Dynnik
{"title":"The Heterogenous Properties of Potassium Glutamate Neurons in the Ventral and Dorsal Regions of the SA1 Hippopotamus","authors":"A. S. Galashin,&nbsp;M. V. Konakov,&nbsp;V. V. Dynnik","doi":"10.1134/S0006350925700642","DOIUrl":null,"url":null,"abstract":"<p>A comparative study of the electrophysiological characteristics of pyramidal (PC) neurons of the dorsal and ventral parts of the CA1 region of the hippocampus of mice was conducted using the patch-clamp method in the “whole cell” configuration. The potassium load was used as a parameter for cell type discrimination (an increase in [K+]o from 3.0 to 8.5 mM in the medium). It has been established that two types of cells with different sensitivities to potassium are found in both parts of the CA1 region. In PC-A type cells, the burst activity caused by a step of current I (from 10 to 200 pA) is potentiated by potassium with an increase in [K+]o to 8.5 mM, whereas in PC-I type cells at currents I &lt; 100 pA there is no effect of potassium loading and at currents ≥125 pA suppression of burst activity is observed. The ratios of the number of PC-A/PC-I cells in the ventral and dorsal regions are 16 : 5 and 8 : 8, respectively. Potassium potentiation of burst activity is higher in ventral PC-A cells than in dorsal cells. The threshold current (Ith) decreases by 2.5 times and a spontaneous burst (pacemaker) activity is manifested only in PC-A cells with potassium loading. The Sag potential and the adaptation index of induced impulse activity are higher in the ventral PC-A cells than in the dorsal cells. The potassium load reduces the Sag potential. An analysis of the voltage characteristics shows that incoming and outgoing (predominantly) slow potassium currents are activated under a potassium load. The currents in the ventral neurons of both types are 1.5–2.0 times lower than in the dorsal neurons (at –100 and +20 mV). Taken together, these data suggest that <span>\\({\\text{K}}_{{\\text{o}}}^{ + }\\)</span>-sensitive ventral PC-A cells can play an important role in hyperexcitation of neural networks and induction of epileptogenesis.</p>","PeriodicalId":493,"journal":{"name":"Biophysics","volume":"70 4","pages":"606 - 618"},"PeriodicalIF":4.0330,"publicationDate":"2026-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysics","FirstCategoryId":"4","ListUrlMain":"https://link.springer.com/article/10.1134/S0006350925700642","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

A comparative study of the electrophysiological characteristics of pyramidal (PC) neurons of the dorsal and ventral parts of the CA1 region of the hippocampus of mice was conducted using the patch-clamp method in the “whole cell” configuration. The potassium load was used as a parameter for cell type discrimination (an increase in [K+]o from 3.0 to 8.5 mM in the medium). It has been established that two types of cells with different sensitivities to potassium are found in both parts of the CA1 region. In PC-A type cells, the burst activity caused by a step of current I (from 10 to 200 pA) is potentiated by potassium with an increase in [K+]o to 8.5 mM, whereas in PC-I type cells at currents I < 100 pA there is no effect of potassium loading and at currents ≥125 pA suppression of burst activity is observed. The ratios of the number of PC-A/PC-I cells in the ventral and dorsal regions are 16 : 5 and 8 : 8, respectively. Potassium potentiation of burst activity is higher in ventral PC-A cells than in dorsal cells. The threshold current (Ith) decreases by 2.5 times and a spontaneous burst (pacemaker) activity is manifested only in PC-A cells with potassium loading. The Sag potential and the adaptation index of induced impulse activity are higher in the ventral PC-A cells than in the dorsal cells. The potassium load reduces the Sag potential. An analysis of the voltage characteristics shows that incoming and outgoing (predominantly) slow potassium currents are activated under a potassium load. The currents in the ventral neurons of both types are 1.5–2.0 times lower than in the dorsal neurons (at –100 and +20 mV). Taken together, these data suggest that \({\text{K}}_{{\text{o}}}^{ + }\)-sensitive ventral PC-A cells can play an important role in hyperexcitation of neural networks and induction of epileptogenesis.

Abstract Image

SA1河马腹侧和背侧谷氨酸钾神经元的异质性
采用膜片钳法在“全细胞”构型下对小鼠海马CA1区背侧和腹侧锥体(PC)神经元电生理特性进行了比较研究。钾负荷被用作细胞类型判别的参数(培养基中的[K+]o从3.0 mM增加到8.5 mM)。已经确定,在CA1区域的两个部分都发现了两种对钾具有不同敏感性的细胞。在PC-A型细胞中,由电流I(从10到200 pA)引起的突发活动被钾增强,[K+] 0增加到8.5 mM,而在电流I和lt; 100 pA的PC-I型细胞中,钾负荷没有影响,电流≥125 pA时观察到突发活动的抑制。腹侧和背侧PC-A/ pc - 1细胞数量之比分别为16:5和8:8。腹侧PC-A细胞的爆发活动钾增强高于背侧细胞。阈值电流(Ith)降低了2.5倍,自发爆发(起搏器)活动仅在钾负荷的PC-A细胞中表现出来。腹侧PC-A细胞的凹陷电位和诱导冲动活动的适应指数高于背侧PC-A细胞。钾负荷降低了下垂电位。电压特性分析表明,在钾负荷下,输入和输出(主要是)慢钾电流被激活。两种类型的腹侧神经元的电流比背侧神经元低1.5-2.0倍(-100和+20 mV)。综上所述,这些数据表明\({\text{K}}_{{\text{o}}}^{ + }\) -敏感的腹侧PC-A细胞在神经网络的过度兴奋和诱导癫痫发生中发挥重要作用。
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
Biophysics
Biophysics Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
1.20
自引率
0.00%
发文量
67
期刊介绍: Biophysics is a multidisciplinary international peer reviewed journal that covers a wide scope of problems related to the main physical mechanisms of processes taking place at different organization levels in biosystems. It includes structure and dynamics of macromolecules, cells and tissues; the influence of environment; energy transformation and transfer; thermodynamics; biological motility; population dynamics and cell differentiation modeling; biomechanics and tissue rheology; nonlinear phenomena, mathematical and cybernetics modeling of complex systems; and computational biology. The journal publishes short communications devoted and review articles.
×
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:604180095
Book学术官方微信
小红书