Evidence map›Paper›PMID 31852909›Full record

ArticleScientific reports2019

Focused ultrasound enhanced intranasal delivery of brain derived neurotrophic factor produces neurorestorative effects in a Parkinson's disease mouse model.

Robin Ji, Morgan Smith, Yusuke Niimi, Maria E Karakatsani, Maria F Murillo, Vernice Jackson-Lewis, Serge Przedborski, Elisa E Konofagou

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Focused Ultrasound for the Treatment of Circuit and Molecular Pathology in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Characterization of microbubble cavitation in theranostic ultrasound-mediated blood-brain barrier opening for gene delivery.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  9. Article
  10. Nose-to-brain drug delivery: from bench to bedside.Translational neurodegeneration · 2025
    Review
  11. Brain sciences · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Research progress on intranasal treatment for Parkinson's disease.Neuroprotection (Chichester, England) · 2024
    Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Transcranial histotripsy parameter study in primary and metastatic murine brain tumor models.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2023
    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

8 authors at 1 institution in 1 country.

Robin JiDepartment of Biomedical Engineering, Columbia University, New York, New York, USA.ORCID http://orcid.org/0000-0003-1361-141X
Morgan SmithDepartment of Biomedical Engineering, Columbia University, New York, New York, USA.
Yusuke NiimiDepartment of Biomedical Engineering, Columbia University, New York, New York, USA.
Maria E KarakatsaniDepartment of Biomedical Engineering, Columbia University, New York, New York, USA.ORCID http://orcid.org/0000-0002-8368-1360
Maria F MurilloDepartment of Biomedical Engineering, Columbia University, New York, New York, USA.
Vernice Jackson-LewisDepartment of Pathology & Cell Biology, Columbia University, New York, New York, USA.
Serge PrzedborskiDepartment of Pathology & Cell Biology, Columbia University, New York, New York, USA.
Elisa E KonofagouDepartment of Biomedical Engineering, Columbia University, New York, New York, USA. ek2191@columbia.edu.
Columbia University · US

Funding

Assessment of Ultrsound-facilitated Neurotherapeutics in Alzheimer's DiseaseR01AG038961 · NIA · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KONOFAGOU, ELISA E. · 2011 to 2020
$5.1M
Optimization of ultrasound-facilitated blood-brain barrier openingR01EB009041 · NIBIB · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KONOFAGOU, ELISA E. · 2008 to 2017
$4.4M
Intranasal delivery through the blood-brain barrier using focused ultrasoundR21EB021103 · NIBIB · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KONOFAGOU, ELISA E. · 2016 to 2018
$488k
NIA NIH HHS R01 AG038961NIBIB NIH HHS R01 EB009041NIBIB NIH HHS R21 EB021103
6 · The paper itself

Abstract

Focused ultrasound-enhanced intranasal (IN + FUS) delivery is a noninvasive approach that utilizes the olfactory pathway to administer pharmacological agents directly to the brain, allowing for a more homogenous distribution in targeted locations compared to IN delivery alone. However, whether such a strategy has therapeutic values, especially in neurodegenerative disorders such as Parkinson's disease (PD), remains to be established. Herein, we evaluated whether the expression of tyrosine hydroxylase (TH), the rate limiting enzyme in dopamine catalysis, could be enhanced by IN + FUS delivery of brain-derived neurotrophic factor (BDNF) in a toxin-based PD mouse model. Mice were put on the subacute dosing regimen of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), producing bilateral degeneration of the nigrostriatal pathway consistent with early-stage PD. MPTP mice then received BDNF intranasally followed by multiple unilateral FUS-induced blood-brain barrier (BBB) openings in the left basal ganglia for three consecutive weeks. Subsequently, mice were survived for two months and were evaluated morphologically and behaviorally to determine the integrity of their nigrostriatal dopaminergic pathways. Mice receiving IN + FUS had significantly increased TH immunoreactivity in the treated hemisphere compared to the untreated hemisphere while mice receiving only FUS-induced BBB opening or no treatment at all did not show any differences. Additionally, behavioral changes were only observed in the IN + FUS treated mice, indicating improved motor control function in the treated hemisphere. These findings demonstrate the robustness of the method and potential of IN + FUS for the delivery of bioactive factors for treatment of neurodegenerative disorder.

Indexed as

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAdministration, IntranasalAnimalsBasal GangliaBlood-Brain BarrierBrainBrain-Derived Neurotrophic FactorCorpus StriatumDisease Models, AnimalDopamineHumansMiceNeuroprotective AgentsParkinson DiseaseParkinson Disease, SecondarySubstantia Nigra1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineBdnf protein, mouseBrain-Derived Neurotrophic FactorDopamineNeuroprotective AgentsTyrosine 3-Monooxygenase

Identifiers

PMID31852909
PMCPMC6920380
OpenAlexW2994735642

What OpenQuestion holds

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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.