Evidence map›Paper›PMID 39867131›Full record

ArticleNeurophotonics2025

Low-cost physiology and behavioral monitor for intravital imaging in small mammals.

Yuntao Li, Alfredo Cardenas-Rivera, Chang Liu, Zhengyi Lu, Jaime Anton, Mohammed Alfadhel, Mohammad A Yaseen

Abstract read
In one paragraph

Article in Neurophotonics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Yuntao LiNortheastern University, Department of Bioengineering, Boston, Massachusetts, United States.
Alfredo Cardenas-RiveraNortheastern University, Department of Bioengineering, Boston, Massachusetts, United States.ORCID https://orcid.org/0000-0001-7960-1842
Chang LiuNortheastern University, Department of Bioengineering, Boston, Massachusetts, United States.
Zhengyi LuNortheastern University, Department of Bioengineering, Boston, Massachusetts, United States.
Jaime AntonNortheastern University, Department of Bioengineering, Boston, Massachusetts, United States.ORCID https://orcid.org/0009-0003-6478-3200
Mohammed AlfadhelNortheastern University, Department of Bioengineering, Boston, Massachusetts, United States.ORCID https://orcid.org/0009-0007-2865-5403
Mohammad A YaseenNortheastern University, Department of Bioengineering, Boston, Massachusetts, United States.ORCID https://orcid.org/0000-0002-4154-152X

Funding

Relating Neuroimmune and Neurovascular Alterations During Alzheimer's Disease ProgressionR01AA027097 · NIAAA · NORTHEASTERN UNIVERSITY · PI YASEEN, MOHAMMAD ABBAS · 2018 to 2022
$2.7M
Modulating blood flow and metabolism in Alzheimer's Disease modelsR21AG085655 · NIA · NORTHEASTERN UNIVERSITY · PI YASEEN, MOHAMMAD ABBAS · 2024 to 2025
$440k
Exploring preclinical amyloid pathology with optical microscopyR56AG058849 · NIA · NORTHEASTERN UNIVERSITY · PI YASEEN, MOHAMMAD ABBAS · 2019 to 2019
$432k
NIAAA NIH HHS R01 AA027097NIA NIH HHS R21 AG085655NIA NIH HHS R56 AG058849
6 · The paper itself

Abstract

Significance: Functional brain imaging experiments in awake animals require meticulous monitoring of animal behavior to screen for spontaneous behavioral events. Although these events occur naturally, they can alter cell signaling and hemodynamic activity in the brain and confound functional brain imaging measurements. Aim: We developed a centralized, user-friendly, and stand-alone platform that includes an animal fixation frame, compact peripheral sensors, and a portable data acquisition system. The affordable, integrated platform can benefit imaging experiments by monitoring animal behavior for motion detection and alertness levels as complementary readouts for brain activity measurements. Approach: A custom acquisition system was designed using a powerful, inexpensive microcomputer. We customized an accelerometer and miniature camera modules for efficient, real-time monitoring of animal motion detection and pupil diameter. We then tested and validated the platform's performance with optical intrinsic signal imaging and GCaMP fluorescence calcium imaging in functional activation experiments in awake mice. Results: The integrated platform shows promise for detecting spontaneous motion and pupil dilation while imaging. Stimulus-induced pupil dilation was found to initiate earlier than cortical hemodynamics with a slower rise time. Compared with neuronal calcium response, stimulus-induced pupil dilation initiated later with a slower rise time. Conclusions: We developed an integrated platform to monitor animal motion and pupil dynamics. The device can be easily coupled and synchronized with optical brain imaging systems to monitor behavior, alertness, and spontaneous motion for awake animal studies.

Indexed as

awake mouse imagingcalcium imagingfunctional activationoptical intrinsic signalpupillometryspontaneous motion

Identifiers

PMID39867131
PMCPMC11759666

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.