• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

视紫红质基因敲除小鼠的视网膜电图。

The electroretinogram of the rhodopsin knockout mouse.

作者信息

Toda K, Bush R A, Humphries P, Sieving P A

机构信息

Department of Ophthalmology, and Programs in Neuroscience and in Bioengineering, University of Michigan, Ann Arbor, USA.

出版信息

Vis Neurosci. 1999 Mar-Apr;16(2):391-8. doi: 10.1017/s0952523899162187.

DOI:10.1017/s0952523899162187
PMID:10367972
Abstract

The electroretinogram (ERG) of the rhodopsin knockout (rho-/-) mouse of Humphries et al. (1997) (Humphries et al., 1997) was studied for evidence of light-evoked rod activity and to describe the cone function. The rho-/- retina develops normal numbers of rod and cone nuclei, but the rods have no outer segments, and no rhodopsin is found by immunohistochemistry. The dark-adapted ERG threshold was elevated 4.7 log units above wild-type (WT) control mice, indicating that any residual rod responses were reduced >50,000-fold, consistent with a complete functional knockout. The dark-adapted rho-/- ERG had a cone waveform, and the spectral sensitivity peaked near 510 nm for both dark-adapted and light-adapted conditions, without evidence of a Purkinje shift. The light-adapted ERG b-wave amplitude of young rho-/- mice was the same as WT. The amplitude remained steady up to postnatal day P47, but thereafter it declined to only 1-2% by P80 when no cone outer segments remained. Cone b-wave threshold of dark-adapted rho-/- mice was -1.07 +/- 0.39 log cd-s/m2 (n = 17), which is 1.27 log units more sensitive than light-adapted thresholds against a rod-suppressing Ganzfeld background of 1.61 log scotopic cd/m2. This indicates that dark-adapted WT responses to still dimmer stimuli are exclusively rod driven with minimal cone intrusion. Above this cone threshold intensity, the dark-adapted b-wave of WT will be a summation of rod and cone responses. Threshold versus intensity (TVI) studies gave no evidence of a rod influence on the mouse cone b-wave.

摘要

对Humphries等人(1997年)的视紫红质基因敲除(rho-/-)小鼠的视网膜电图(ERG)进行了研究,以寻找光诱发视杆细胞活动的证据并描述视锥细胞功能。rho-/-视网膜中视杆细胞核和视锥细胞核的数量发育正常,但视杆细胞没有外节,免疫组织化学检测未发现视紫红质。暗适应的ERG阈值比野生型(WT)对照小鼠高4.7个对数单位,这表明任何残留的视杆细胞反应都降低了>50000倍,这与完全功能性敲除一致。暗适应的rho-/- ERG具有视锥细胞波形,在暗适应和明适应条件下,光谱敏感度在510 nm附近达到峰值,没有浦肯野氏位移的证据。幼年rho-/-小鼠明适应的ERG b波振幅与WT相同。该振幅在出生后第47天之前保持稳定,但此后在出生后第80天下降到仅1%-2%,此时视锥细胞外节已不存在。暗适应的rho-/-小鼠视锥细胞b波阈值为-1.07±0.39 log cd-s/m2(n = 17),在1.61 log scotopic cd/m2的抑制视杆细胞的全视野背景下,比明适应阈值敏感1.27个对数单位。这表明暗适应的WT对更暗淡刺激的反应完全由视杆细胞驱动,视锥细胞的干扰最小。高于该视锥细胞阈值强度时,暗适应的WT的b波将是视杆细胞和视锥细胞反应的总和。阈值与强度(TVI)研究未发现视杆细胞对小鼠视锥细胞b波有影响。

相似文献

1
The electroretinogram of the rhodopsin knockout mouse.视紫红质基因敲除小鼠的视网膜电图。
Vis Neurosci. 1999 Mar-Apr;16(2):391-8. doi: 10.1017/s0952523899162187.
2
Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions.两种全色突变小鼠在明适应过程中的 ERG 变化:对光感受器-双极细胞通路相互作用的影响。
Invest Ophthalmol Vis Sci. 2019 Aug 1;60(10):3680-3688. doi: 10.1167/iovs.19-27242.
3
Genetic dissection of rod and cone pathways in the dark-adapted mouse retina.暗适应小鼠视网膜中视杆和视锥通路的遗传学剖析。
J Neurophysiol. 2009 Sep;102(3):1945-55. doi: 10.1152/jn.00142.2009. Epub 2009 Jul 8.
4
Rod-driven OFF pathway responses in the distal retina: dark-adapted flicker electroretinogram in mouse.杆驱动的 OFF 通路反应在视网膜的远端:小鼠暗适应闪烁视网膜电图。
PLoS One. 2012;7(8):e43856. doi: 10.1371/journal.pone.0043856. Epub 2012 Aug 24.
5
Biphasic photoreceptor degeneration induced by light in a T17M rhodopsin mouse model of cone bystander damage.在T17M视紫红质小鼠模型中,光诱导的双相光感受器变性导致视锥细胞旁观者损伤。
Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2956-65. doi: 10.1167/iovs.08-3116. Epub 2009 Jan 10.
6
Age-related changes in Cngb1-X1 knockout mice: prolonged cone survival.Cngb1-X1基因敲除小鼠的年龄相关变化:视锥细胞存活时间延长。
Doc Ophthalmol. 2012 Jun;124(3):163-75. doi: 10.1007/s10633-012-9317-2. Epub 2012 Feb 26.
7
Evaluation of the rhodopsin knockout mouse as a model of pure cone function.视紫红质基因敲除小鼠作为纯视锥功能模型的评估。
Invest Ophthalmol Vis Sci. 2001 Feb;42(2):506-13.
8
The status of cones in the rhodopsin mutant P23H-3 retina: light-regulated damage and repair in parallel with rods.视紫红质突变体P23H-3视网膜中视锥细胞的状态:与视杆细胞平行的光调节损伤和修复
Invest Ophthalmol Vis Sci. 2008 Mar;49(3):1116-25. doi: 10.1167/iovs.07-1158.
9
Using Silent Substitution to Track the Mesopic Transition From Rod- to Cone-Based Vision in Mice.利用沉默替代法追踪小鼠从基于视杆细胞到基于视锥细胞视觉的中间视觉转变。
Invest Ophthalmol Vis Sci. 2016 Jan 1;57(1):276-87. doi: 10.1167/iovs.15-18197.
10
A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction.一种伴有视锥细胞ON通路功能障碍的独特类型的先天性静止性夜盲。
Ophthalmology. 2002 Mar;109(3):575-83. doi: 10.1016/s0161-6420(01)00981-2.

引用本文的文献

1
Downregulation of rhodopsin is an effective therapeutic strategy in ameliorating peripherin-2-associated inherited retinal disorders.下调视蛋白是改善 peripherin-2 相关遗传性视网膜疾病的有效治疗策略。
Nat Commun. 2024 Jun 4;15(1):4756. doi: 10.1038/s41467-024-48846-5.
2
Chromophore supply modulates cone function and survival in retinitis pigmentosa mouse models.生色团供应调节视锥细胞功能和在色素性视网膜炎小鼠模型中的存活。
Proc Natl Acad Sci U S A. 2023 Jun 6;120(23):e2217885120. doi: 10.1073/pnas.2217885120. Epub 2023 May 30.
3
Electroretinogram responses in myopia: a review.
近视的视网膜电图反应:综述。
Doc Ophthalmol. 2022 Oct;145(2):77-95. doi: 10.1007/s10633-021-09857-5. Epub 2021 Nov 17.
4
Rs1h exon 3-del rat model of X-linked retinoschisis with early onset and rapid phenotype is rescued by RS1 supplementation.X 连锁性视网膜劈裂症 Rs1h 外显子 3 缺失型大鼠模型具有早发和快速表型特征,通过 RS1 补充得以挽救。
Gene Ther. 2022 Aug;29(7-8):431-440. doi: 10.1038/s41434-021-00290-6. Epub 2021 Sep 22.
5
Photoperiodic regulation of dopamine signaling regulates seasonal changes in retinal photosensitivity in mice.光周期对多巴胺信号的调节调控了小鼠视网膜感光性的季节性变化。
Sci Rep. 2021 Jan 19;11(1):1843. doi: 10.1038/s41598-021-81540-w.
6
Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances.用于退化视网膜的光遗传学基因治疗:最新进展
Front Neurosci. 2020 Nov 11;14:570909. doi: 10.3389/fnins.2020.570909. eCollection 2020.
7
SARM1 deficiency promotes rod and cone photoreceptor cell survival in a model of retinal degeneration.SARM1 缺乏可促进视网膜变性模型中视杆和视锥光感受器细胞的存活。
Life Sci Alliance. 2020 Apr 20;3(5). doi: 10.26508/lsa.201900618. Print 2020 May.
8
Optical Coherence Tomography of Animal Models of Retinitis Pigmentosa: From Animal Studies to Clinical Applications.视网膜色素变性动物模型的光学相干断层扫描:从动物研究到临床应用。
Biomed Res Int. 2019 Oct 30;2019:8276140. doi: 10.1155/2019/8276140. eCollection 2019.
9
Increase in electroretinogram rod-driven peak frequency of oscillatory potentials and dark-adapted responses in a cohort of myopia patients.一组近视患者的视网膜电图振荡电位的视杆细胞驱动峰值频率和暗适应反应增加。
Doc Ophthalmol. 2020 Apr;140(2):189-199. doi: 10.1007/s10633-019-09732-4. Epub 2019 Oct 28.
10
Visual Contrast Sensitivity Correlates to the Retinal Degeneration in Rhodopsin Knockout Mice.视觉对比敏感度与视紫红质敲除小鼠的视网膜变性相关。
Invest Ophthalmol Vis Sci. 2019 Oct 1;60(13):4196-4204. doi: 10.1167/iovs.19-26966.