Evidence map›Paper›PMID 29463867›Full record

ArticleScientific reports2018

Optogenetic Tractography for anatomo-functional characterization of cortico-subcortical neural circuits in non-human primates.

S Senova, C Poupon, J Dauguet, H J Stewart, G P Dugué, C Jan, K Hosomi, G S Ralph, L Barnes, X Drouot and 10 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Lentiviral delivered aflibercept OXB-203 for treatment of neovascular AMD.Molecular therapy. Methods & clinical development · 2023
    Article
  3. Towards translational optogenetics.Nature biomedical engineering · 2023
    Review
  4. Review
  5. Review
  6. Article
  7. Review
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

20 authors at 6 institutions in 3 countries.

S SenovaLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France.
C PouponUnité d'IRM et de Spectroscopie(UNIRS), NeuroSpin, I²BM, CEA, Saclay, France.
J DauguetLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France.
H J StewartOxford BioMedica (UK) Limited, Windrush Court, Transport Way, Oxford, UK.
G P DuguéCNRS UMR 8197, Inserm U1024, institut de Biologie de l'Ecole Normale Supérieure, Paris, France.
C JanLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France.
K HosomiLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France.
G S RalphCNRS UMR 8197, Inserm U1024, institut de Biologie de l'Ecole Normale Supérieure, Paris, France.
L BarnesCNRS UMR 8197, Inserm U1024, institut de Biologie de l'Ecole Normale Supérieure, Paris, France.
X DrouotFunctional Explorations department, Assistance Publique-Hôpitaux de Paris (APHP), Groupe Henri-Mondor Albert-Chenevier, Université Paris 12 UPEC, Faculté de Médecine, F-94010, Créteil, France.
C PouzatMAP5, Mathématiques Appliquées Paris 5, CNRS UMR 8145, Paris, France.ORCID 0000-0002-2844-8099
J F ManginLaboratoire de Neuroanatomie Assistée par Ordinateur (LNAO), CEA, Neurospin, Saclay, France.
F PainIMNC-IN2P3, Université Paris Sud, Orsay, France.
I DoignonINSERM UMRs 1174, Laboratory of Cellular interactions and liver physiopathology, Université Paris-Sud, Batiment 443, Orsay, France.
R Aron-BadinLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France.
E BrouilletLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France.ORCID 0000-0001-6322-7403
E S BoydenMassachusetts Institute of Technology, Media Lab, Boston, United States.
K A MitrophanousOxford BioMedica (UK) Limited, Windrush Court, Transport Way, Oxford, UK.
P HantrayeLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France.
S PalfiLaboratoire des Maladies Neurodégénératives, UMR9199, CEA, CNRS, Université Paris-Sud, Univ Paris Saclay, MIRCen, I²BM, CEA, Fontenay-aux-Roses, 92265, France. stephane.palfi@aphp.fr.
Université Paris-Sud · FRCentre National de la Recherche Scientifique · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FROxford BioMedica (United Kingdom) · GBMassachusetts Institute of Technology · USUniversité Paris-Est Créteil · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dissecting neural circuitry in non-human primates (NHP) is crucial to identify potential neuromodulation anatomical targets for the treatment of pharmacoresistant neuropsychiatric diseases by electrical neuromodulation. How targets of deep brain stimulation (DBS) and cortical targets of transcranial magnetic stimulation (TMS) compare and might complement one another is an important question. Combining optogenetics and tractography may enable anatomo-functional characterization of large brain cortico-subcortical neural pathways. For the proof-of-concept this approach was used in the NHP brain to characterize the motor cortico-subthalamic pathway (m_CSP) which might be involved in DBS action mechanism in Parkinson's disease (PD). Rabies-G-pseudotyped and Rabies-G-VSVg-pseudotyped EIAV lentiviral vectors encoding the opsin ChR2 gene were stereotaxically injected into the subthalamic nucleus (STN) and were retrogradely transported to the layer of the motor cortex projecting to STN. A precise anatomical mapping of this pathway was then performed using histology-guided high angular resolution MRI tractography guiding accurately cortical photostimulation of m_CSP origins. Photoexcitation of m_CSP axon terminals or m_CSP cortical origins modified the spikes distribution for photosensitive STN neurons firing rate in non-equivalent ways. Optogenetic tractography might help design preclinical neuromodulation studies in NHP models of neuropsychiatric disease choosing the most appropriate target for the tested hypothesis.

Indexed as

ConnectomeAction PotentialsAnimalsGenes, ReporterGenetic VectorsLentivirusMacaca mulattaMagnetic Resonance ImagingMaleMotor CortexNerve NetOpsinsOptogeneticsSubthalamic NucleusTransduction, GeneticOpsins

Identifiers

PMID29463867
PMCPMC5820256
OpenAlexW2806547166

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.