Evidence map›Paper›PMID 36107146›Full record

ArticleeLife2022

3D optogenetic control of arteriole diameter in vivo.

Philip J O'Herron, David A Hartmann, Kun Xie, Prakash Kara, Andy Y Shih

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Single celliScience · 2023
    Article
  9. 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

5 authors at 3 institutions in 1 country.

Philip J O'HerronDepartment of Physiology, Augusta University, Augusta, United States.ORCID 0000-0002-8137-9432
David A HartmannDepartment of Neuroscience, Medical University of South Carolina, Charleston, United States.
Kun XieDepartment of Physiology, Augusta University, Augusta, United States.
Prakash KaraDepartment of Neuroscience, Medical University of South Carolina, Charleston, United States.ORCID 0000-0002-4285-1634
Andy Y ShihDepartment of Neuroscience, Medical University of South Carolina, Charleston, United States.
Medical University of South Carolina · USAugusta University · USUniversity of Minnesota · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Neurons, Vessels and Voxels: Multi-modal Imaging of Layer Specific SignalsR01MH111447 · NIMH · UNIVERSITY OF MINNESOTA · PI KARA, PRAKASH, NASELARIS, THOMAS P · 2016 to 2020
$5.0M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR001451 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FEGHALI-BOSTWICK, CAROL A. · 2015 to 2024
$4.6M
Deciphering the Cerebral Microinfarct and its Role in Vascular Cognitive ImpairmentR01NS097775 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI SHIH, ANDY Y · 2017 to 2021
$3.2M
Pericyte structural plasticity and cerebrovascular healthR01AG062738 · NIA · SEATTLE CHILDREN'S HOSPITAL · PI SHIH, ANDY Y · 2020 to 2024
$3.0M
Cytoskeletal Dynamics of Brain Pericytes and Impact on Capillary FlowR21NS106138 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI SHIH, ANDY Y · 2018 to 2019
$518k
The Physiological Mechanisms and Role in Neural Coding of Functional HyperemiaR21NS110069 · NINDS · AUGUSTA UNIVERSITY · PI O'HERRON, PHILIP · 2019 to 2020
$421k
The impact of reduced blood flow early in Alzheimer's disease on neuronal function.R03AG070507 · NIA · AUGUSTA UNIVERSITY · PI O'HERRON, PHILIP · 2021 to 2021
$308k
A Potential New Role for Pericytes in Functional HyperemiaF30NS096868 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HARTMANN, DAVID ANTHONY · 2016 to 2019
$177k
NCATS NIH HHS TL1 TR001451NCATS NIH HHS UL1 TR001450NIA NIH HHS R01 AG062738NIA NIH HHS R03 AG070507NIMH NIH HHS R01 MH111447NINDS NIH HHS F30 NS096868NINDS NIH HHS R01 NS097775NINDS NIH HHS R21 NS106138NINDS NIH HHS R21 NS110069
6 · The paper itself

Abstract

Modulation of brain arteriole diameter is critical for maintaining cerebral blood pressure and controlling regional hyperemia during neural activity. However, studies of hemodynamic function in health and disease have lacked a method to control arteriole diameter independently with high spatiotemporal resolution. Here, we describe an all-optical approach to manipulate and monitor brain arteriole contractility in mice in three dimensions using combined in vivo two-photon optogenetics and imaging. The expression of the red-shifted excitatory opsin, ReaChR, in vascular smooth muscle cells enabled rapid and repeated vasoconstriction controlled by brief light pulses. Two-photon activation of ReaChR using a spatial light modulator produced highly localized constrictions when targeted to individual arterioles within the neocortex. We demonstrate the utility of this method for examining arteriole contractile dynamics and creating transient focal blood flow reductions. Additionally, we show that optogenetic constriction can be used to reshape vasodilatory responses to sensory stimulation, providing a valuable tool to dissociate blood flow changes from neural activity.

Indexed as

NeocortexOptogeneticsAnimalsArteriolesHemodynamicsMiceOpsinsOpsinsblood flowmouseneuroscienceoptogeneticstwo-photonvascular

Identifiers

PMID36107146
PMCPMC9481242
OpenAlexW4295902280

What OpenQuestion 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 OpenQuestion graph.