Evidence map›Paper›PMID 38895451›Full record

ArticlebioRxiv : the preprint server for biology2024

Fiber-based Probes for Electrophysiology, Photometry, Optical and Electrical Stimulation, Drug Delivery, and Fast-Scan Cyclic Voltammetry In Vivo.

Nicolette Driscoll, Marc-Joseph Antonini, Taylor M Cannon, Pema Maretich, Greatness Olaitan, Valerie Doan Phi Van, Keisuke Nagao, Atharva Sahasrabudhe, Emmanuel Vargas, Sydney Hunt and 5 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

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

15 authors.

Nicolette DriscollMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0001-8364-460X
Marc-Joseph AntoniniMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-9774-1483
Taylor M CannonMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0001-5776-1079
Pema MaretichMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0001-5058-812X
Greatness OlaitanThe University of Virginia, Charlottesville, VA 22904.
Valerie Doan Phi VanMassachusetts Institute of Technology, Cambridge, MA 02139.
Keisuke NagaoMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0009-0002-2296-1817
Atharva SahasrabudheMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-2615-2470
Emmanuel VargasMassachusetts Institute of Technology, Cambridge, MA 02139.
Sydney HuntStanford University, Stanford, CA 94305.
Melissa HummelMassachusetts Institute of Technology, Cambridge, MA 02139.
Sanju MupparajuMassachusetts Institute of Technology, Cambridge, MA 02139.
Alan JasanoffMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-2834-6359
Jill VentonThe University of Virginia, Charlottesville, VA 22904.
Polina AnikeevaMassachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0001-6495-5197

Funding

Fusion of nanomagnetic and viral tools to interrogate brain-body circuitsDP1AT011991 · NCCIH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI ANIKEEVA, POLINA O · 2021 to 2025
$5.3M
Multiplexed neurochemical methods to understand adenosine neuromodulationR01NS121014 · NINDS · UNIVERSITY OF VIRGINIA · PI B. JILL VENTON · 2022 to 2026
$3.0M
Optogenetics to improve hand function after spinal cord injury.R01NS115025 · NINDS · UNIVERSITY OF WASHINGTON · PI ANIKEEVA, POLINA O, MORITZ, CHET T. · 2020 to 2023
$2.4M
Tunable Carbon Electrodes for in vivo Neurotransmitter DetectionR01NS125663 · NINDS · UNIVERSITY OF VIRGINIA · PI B. JILL VENTON · 2022 to 2026
$2.2M
NCCIH NIH HHS DP1 AT011991NINDS NIH HHS R01 NS115025NINDS NIH HHS R01 NS121014NINDS NIH HHS R01 NS125663
6 · The paper itself

Abstract

Recording and modulation of neuronal activity enables the study of brain function in health and disease. While translational neuroscience relies on electrical recording and modulation techniques, mechanistic studies in rodent models leverage genetic precision of optical methods, such as optogenetics and imaging of fluorescent indicators. In addition to electrical signal transduction, neurons produce and receive diverse chemical signals which motivate tools to probe and modulate neurochemistry. Although the past decade has delivered a wealth of technologies for electrophysiology, optogenetics, chemical sensing, and optical recording, combining these modalities within a single platform remains challenging. This work leverages materials selection and convergence fiber drawing to permit neural recording, electrical stimulation, optogenetics, fiber photometry, drug and gene delivery, and voltammetric recording of neurotransmitters within individual fibers. Composed of polymers and non-magnetic carbon-based conductors, these fibers are compatible with magnetic resonance imaging, enabling concurrent stimulation and whole-brain monitoring. Their utility is demonstrated in studies of the mesolimbic reward pathway by simultaneously interfacing with the ventral tegmental area and nucleus accumbens in mice and characterizing the neurophysiological effects of a stimulant drug. This study highlights the potential of these fibers to probe electrical, optical, and chemical signaling across multiple brain regions in both mechanistic and translational studies.

Indexed as

fiber-based interfacefiber-photometryFSCVmultifunctional neural probeneuromodulation

Identifiers

PMID38895451
PMCPMC11185794

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.