Evidence map›Paper›PMID 38725801›Full record

ArticleNeurophotonics2024

Toward a brighter constellation: multiorgan neuroimaging of neural and vascular dynamics in the spinal cord and brain.

Dmitrijs Celinskis, Christopher J Black, Jeremy Murphy, Adriel Barrios-Anderson, Nina G Friedman, Nathan C Shaner, Carl Y Saab, Manuel Gomez-Ramirez, David A Borton, Christopher I Moore

Abstract read
In one paragraph

Article in Neurophotonics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Dmitrijs CelinskisCarney Institute for Brain Science, Providence, Rhode Island, United States.ORCID https://orcid.org/0000-0002-8580-7924
Christopher J BlackCarney Institute for Brain Science, Providence, Rhode Island, United States.
Jeremy MurphyCarney Institute for Brain Science, Providence, Rhode Island, United States.
Adriel Barrios-AndersonCarney Institute for Brain Science, Providence, Rhode Island, United States.
Nina G FriedmanCarney Institute for Brain Science, Providence, Rhode Island, United States.
Nathan C ShanerUniversity of California San Diego, School of Medicine, La Jolla, California, United States.ORCID https://orcid.org/0000-0002-0148-0769
Carl Y SaabCleveland Clinic Lerner Research Institute, Neurological Institute, Department of Biomedical Engineering, Cleveland, Ohio, United States.
Manuel Gomez-RamirezUniversity of Rochester, School of Arts and Sciences, Rochester, New York, United States.
David A BortonCarney Institute for Brain Science, Providence, Rhode Island, United States.
Christopher I MooreCarney Institute for Brain Science, Providence, Rhode Island, United States.

Funding

BioLuminescent OptoGenetics (BL-OG): A Novel and Versatile Strategy for NeuromodulationU01NS099709 · NINDS · CENTRAL MICHIGAN UNIVERSITY · PI HOCHGESCHWENDER, UTE H, MOORE, CHRISTOPHER I · 2016 to 2018
$2.4M
Spatiotemporal Coding in the Pain Circuit Along the Spine-brain ContinuumR01NS108414 · NINDS · RHODE ISLAND HOSPITAL · PI BORTON, DAVID ALLENSON, SAAB, CARL Y · 2018 to 2023
$2.0M
NINDS NIH HHS R01 NS108414NINDS NIH HHS U01 NS099709
6 · The paper itself

Abstract

Significance: Pain comprises a complex interaction between motor action and somatosensation that is dependent on dynamic interactions between the brain and spinal cord. This makes understanding pain particularly challenging as it involves rich interactions between many circuits (e.g., neural and vascular) and signaling cascades throughout the body. As such, experimentation on a single region may lead to an incomplete and potentially incorrect understanding of crucial underlying mechanisms. Aim: We aimed to develop and validate tools to enable detailed and extended observation of neural and vascular activity in the brain and spinal cord. The first key set of innovations was targeted to developing novel imaging hardware that addresses the many challenges of multisite imaging. The second key set of innovations was targeted to enabling bioluminescent (BL) imaging, as this approach can address limitations of fluorescent microscopy including photobleaching, phototoxicity, and decreased resolution due to scattering of excitation signals. Approach: We designed 3D-printed brain and spinal cord implants to enable effective surgical implantations and optical access with wearable miniscopes or an open window (e.g., for one- or two-photon microscopy or optogenetic stimulation). We also tested the viability for BL imaging and developed a novel modified miniscope optimized for these signals (BLmini). Results: We describe "universal" implants for acute and chronic simultaneous brain-spinal cord imaging and optical stimulation. We further describe successful imaging of BL signals in both foci and a new miniscope, the "BLmini," which has reduced weight, cost, and form-factor relative to standard wearable miniscopes. Conclusions: The combination of 3D-printed implants, advanced imaging tools, and bioluminescence imaging techniques offers a coalition of methods for understanding spinal cord-brain interactions. Our work has the potential for use in future research into neuropathic pain and other sensory disorders and motor behavior.

Indexed as

bioluminescencebrainfluorescenceimplantable windowminiscopemultiorgan imagingsensory processingspinal cordtwo-photon

Identifiers

PMID38725801
PMCPMC11079446

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.