Evidence map›Paper›PMID 37248385›Full record

ArticleCommunications biology2023

High-resolution structural and functional retinal imaging in the awake behaving mouse.

Guanping Feng, Aby Joseph, Kosha Dholakia, Fei Shang, Charles W Pfeifer, Derek Power, Krishnan Padmanabhan, Jesse Schallek

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Guanping FengDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, 14620, USA.
Aby JosephCenter for Visual Science, University of Rochester, Rochester, NY, 14627, USA.
Kosha DholakiaDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, 14620, USA.
Fei ShangCenter for Visual Science, University of Rochester, Rochester, NY, 14627, USA.
Charles W PfeiferCenter for Visual Science, University of Rochester, Rochester, NY, 14627, USA.ORCID 0000-0002-7579-2984
Derek PowerCenter for Visual Science, University of Rochester, Rochester, NY, 14627, USA.
Krishnan PadmanabhanCenter for Visual Science, University of Rochester, Rochester, NY, 14627, USA.
Jesse SchallekCenter for Visual Science, University of Rochester, Rochester, NY, 14627, USA. jschall3@ur.rochester.edu.ORCID 0000-0002-6337-4187
University of Rochester · US

Funding

VISUAL SCIENCE RESEARCH CTR SUPPORTP30EY001319 · NEI · UNIVERSITY OF ROCHESTER · PI Susana Marcos · 1985 to 2026
$17.5M
University of Rochester Intellectual and Developmental Disabilities Research CenterP50HD103536 · NICHD · UNIVERSITY OF ROCHESTER · PI JOHN J FOXE, Anna K Majewska · 2020 to 2026
$9.8M
Non-invasive, living histology of capillary structure and single cell blood flow in mouse model of diabetic retinopathyR01EY028293 · NEI · UNIVERSITY OF ROCHESTER · PI SCHALLEK, JESSE BARRETT · 2017 to 2025
$4.2M
in vivo imaging of transplanted human induced-Pluripotent Stem Cell (iPSC) derived neurons to model neurological and psychiatric disordersR01MH113924 · NIMH · UNIVERSITY OF ROCHESTER · PI PADMANABHAN, KRISHNAN · 2017 to 2021
$2.3M
NEI NIH HHS P30 EY001319NEI NIH HHS R01 EY028293NICHD NIH HHS P50 HD103536NIMH NIH HHS R01 MH113924
6 · The paper itself

Abstract

The laboratory mouse has provided tremendous insight to the underpinnings of mammalian central nervous system physiology. In recent years, it has become possible to image single neurons, glia and vascular cells in vivo by using head-fixed preparations combined with cranial windows to study local networks of activity in the living brain. Such approaches have also succeeded without the use of general anesthesia providing insights to the natural behaviors of the central nervous system. However, the same has not yet been developed for the eye, which is constantly in motion. Here we characterize a novel head-fixed preparation that enables high-resolution adaptive optics retinal imaging at the single-cell level in awake-behaving mice. We reveal three new functional attributes of the normal eye that are overlooked by anesthesia: 1) High-frequency, low-amplitude eye motion of the mouse that is only present in the awake state 2) Single-cell blood flow in the mouse retina is reduced under anesthesia and 3) Mouse retinae thicken in response to ketamine/xylazine anesthesia. Here we show key benefits of the awake-behaving preparation that enables study of retinal physiology without anesthesia to study the normal retinal physiology in the mouse.

Indexed as

KetamineWakefulnessAnimalsDiagnostic ImagingMammalsMiceRetinaXylazineKetamineXylazine

Identifiers

PMID37248385
PMCPMC10227058
OpenAlexW4378648128

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.