牛视网膜离体灌注-视网膜功能药理研究的灵敏工具

Matthias Lüke , Marco Weiergräber , Carl Brand , Siarhei A. Siapich , Mohammed Banat , Jürgen Hescheler , Christoph Lüke , Toni Schneider
{"title":"牛视网膜离体灌注-视网膜功能药理研究的灵敏工具","authors":"Matthias Lüke ,&nbsp;Marco Weiergräber ,&nbsp;Carl Brand ,&nbsp;Siarhei A. Siapich ,&nbsp;Mohammed Banat ,&nbsp;Jürgen Hescheler ,&nbsp;Christoph Lüke ,&nbsp;Toni Schneider","doi":"10.1016/j.brainresprot.2005.09.001","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>The electroretinogram (ERG) of the isolated bovine retina serves as a proven criterion of retinal activity. It is used as a sensitive pharmacological tool for testing effects of applied drugs and toxins on photoreceptors, and higher order neurons that contribute to the generation of the b-wave. Following isolation and detachment from the underlying </span>pigment<span> epithelium, part of the retina was mounted into a closed chamber and perfused by a nutrient solution. Flow rate of the nutrient solution and its ingredients, incubation temperature and light intensity were optimised empirically to achieve a maximum b-wave amplitude. Under these conditions, a reproducible, high-resolution ERG can be stably recorded for more than 10 h with sufficient oxygenation found to be a prerequisite for the long-lasting stability. Addition of L(+)glutamate to the nutrient solutions was not anymore beneficial for the b-wave amplitude. A well-known inhibitor of oxidative phosphorylation (KCN) and antagonists of voltage-gated Ca</span></span><sup>2+</sup> channels (isradipine, ω-conotoxin-GVIA and NiCl<sub>2</sub>) were used to prove the validity of the test system. The recording of the ERG from the isolated and perfused bovine retina serves as a valuable physiological model for a neuronal network in which important questions related to the retinal signalling and metabolism can be investigated.</p></div>","PeriodicalId":79477,"journal":{"name":"Brain research. Brain research protocols","volume":"16 1","pages":"Pages 27-36"},"PeriodicalIF":0.0000,"publicationDate":"2005-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.brainresprot.2005.09.001","citationCount":"50","resultStr":"{\"title\":\"The isolated perfused bovine retina—A sensitive tool for pharmacological research on retinal function\",\"authors\":\"Matthias Lüke ,&nbsp;Marco Weiergräber ,&nbsp;Carl Brand ,&nbsp;Siarhei A. Siapich ,&nbsp;Mohammed Banat ,&nbsp;Jürgen Hescheler ,&nbsp;Christoph Lüke ,&nbsp;Toni Schneider\",\"doi\":\"10.1016/j.brainresprot.2005.09.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>The electroretinogram (ERG) of the isolated bovine retina serves as a proven criterion of retinal activity. It is used as a sensitive pharmacological tool for testing effects of applied drugs and toxins on photoreceptors, and higher order neurons that contribute to the generation of the b-wave. Following isolation and detachment from the underlying </span>pigment<span> epithelium, part of the retina was mounted into a closed chamber and perfused by a nutrient solution. Flow rate of the nutrient solution and its ingredients, incubation temperature and light intensity were optimised empirically to achieve a maximum b-wave amplitude. Under these conditions, a reproducible, high-resolution ERG can be stably recorded for more than 10 h with sufficient oxygenation found to be a prerequisite for the long-lasting stability. Addition of L(+)glutamate to the nutrient solutions was not anymore beneficial for the b-wave amplitude. A well-known inhibitor of oxidative phosphorylation (KCN) and antagonists of voltage-gated Ca</span></span><sup>2+</sup> channels (isradipine, ω-conotoxin-GVIA and NiCl<sub>2</sub>) were used to prove the validity of the test system. The recording of the ERG from the isolated and perfused bovine retina serves as a valuable physiological model for a neuronal network in which important questions related to the retinal signalling and metabolism can be investigated.</p></div>\",\"PeriodicalId\":79477,\"journal\":{\"name\":\"Brain research. Brain research protocols\",\"volume\":\"16 1\",\"pages\":\"Pages 27-36\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.brainresprot.2005.09.001\",\"citationCount\":\"50\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain research. Brain research protocols\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1385299X05000851\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain research. Brain research protocols","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1385299X05000851","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 50

摘要

视网膜电图(ERG)的分离牛视网膜可作为视网膜活动的一个证明标准。它被用作一种敏感的药理学工具,用于测试应用药物和毒素对光感受器的影响,以及有助于产生b波的高阶神经元。分离并脱离下层色素上皮后,将部分视网膜装入封闭腔内,用营养液灌注。经验优化了营养液及其成分的流速、培养温度和光照强度,以获得最大的b波振幅。在这些条件下,一个可重复的,高分辨率的ERG可以稳定地记录超过10小时,并且足够的氧合被认为是持久稳定性的先决条件。在营养液中添加L(+)谷氨酸对b波振幅不再有利。一种著名的氧化磷酸化抑制剂(KCN)和电压门控制的Ca2+通道拮抗剂(isradipine, ω-conotoxin-GVIA和NiCl2)被用来证明测试系统的有效性。从分离和灌注的牛视网膜中记录的ERG可以作为一个有价值的神经网络生理模型,其中与视网膜信号传导和代谢相关的重要问题可以被研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
The isolated perfused bovine retina—A sensitive tool for pharmacological research on retinal function

The electroretinogram (ERG) of the isolated bovine retina serves as a proven criterion of retinal activity. It is used as a sensitive pharmacological tool for testing effects of applied drugs and toxins on photoreceptors, and higher order neurons that contribute to the generation of the b-wave. Following isolation and detachment from the underlying pigment epithelium, part of the retina was mounted into a closed chamber and perfused by a nutrient solution. Flow rate of the nutrient solution and its ingredients, incubation temperature and light intensity were optimised empirically to achieve a maximum b-wave amplitude. Under these conditions, a reproducible, high-resolution ERG can be stably recorded for more than 10 h with sufficient oxygenation found to be a prerequisite for the long-lasting stability. Addition of L(+)glutamate to the nutrient solutions was not anymore beneficial for the b-wave amplitude. A well-known inhibitor of oxidative phosphorylation (KCN) and antagonists of voltage-gated Ca2+ channels (isradipine, ω-conotoxin-GVIA and NiCl2) were used to prove the validity of the test system. The recording of the ERG from the isolated and perfused bovine retina serves as a valuable physiological model for a neuronal network in which important questions related to the retinal signalling and metabolism can be investigated.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Author Index Selective capture of endothelial and perivascular cells from brain microvessels using laser capture microdissection Real-time visualization and characterization of liposomal delivery into the monkey brain by magnetic resonance imaging Episodic-like memory in mice: Simultaneous assessment of object, place and temporal order memory The isolated perfused bovine retina—A sensitive tool for pharmacological research on retinal function
×
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