Evidence map›Paper›PMID 41427361›Full record

ArticlebioRxiv : the preprint server for biology2025

Electroconvulsive Therapy Induces Dopaminergic Axon Regeneration, Corticostriatal Remodeling, and Restoration of Motor Function in Parkinsonian Mice.

Anika Frank, Se Joon Choi, Jonas Bendig, Anna S Monzel, Adrienne C Ferguson, Siham Boumhaouad, Martin Picard, Eugene V Mosharov, David Sulzer

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

9 authors.

Anika FrankDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.
Se Joon ChoiNew York State Psychiatric Institute, RFMH, New York, NY, USA.
Jonas BendigDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.
Anna S MonzelDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.
Adrienne C FergusonDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.
Siham BoumhaouadDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.
Martin PicardDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.
Eugene V MosharovDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.ORCID 0000-0002-0229-7114
David SulzerDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University Irving Medical Center (CUIMC), New York, NY, USA.

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
NCI NIH HHS P30 CA013696
6 · The paper itself

Abstract

Parkinson's disease (PD) is characterized by the progressive degeneration of midbrain dopaminergic neurons with loss of axonal dopamine neurotransmission in the dorsal striatum, leading to striatal circuit dysfunction and debilitating motor symptoms. Current therapies provide symptomatic relief but do not restore lost neuronal function. Decades of clinical observations have reported the unexpected observation that electroconvulsive therapy (ECT), a standard treatment for refractory neuropsychiatric disorders, can incidentally alleviate motor symptoms in PD patients, yet the underlying mechanisms remain unknown. Here, we report that in the unilateral 6-hydroxydopamine (6-OHDA) mouse model of PD, two weeks of repeated ECT produced robust and sustained motor recovery, with improvements in locomotion and sensorimotor asymmetry persisting for at least 30 days post-treatment. Remarkably, ECT induced dopaminergic axonal sprouting from surviving dopaminergic neurons with cell bodies located at the substantia nigra-ventral tegmental border, leading to a partial recovery of striatal dopaminergic axonal reinnervation. In striatal direct pathway spiny projection neurons (dSPNs), which exhibit pathological hyperexcitability and spine loss following dopamine depletion, ECT normalized both corticostriatal synaptic responses and spine density. Consistently, ECT upregulated gene transcripts involved in cytoskeletal remodeling while downregulating those associated with glutamatergic signaling and neuronal excitability. These changes were accompanied by a coordinated transcriptional shift toward enhanced mitochondrial anabolic capacity and energy production, including increased expression of genes involved in ATP and Coenzyme Q biosynthesis. Together, these findings demonstrate that ECT can partially restore basal ganglia circuitry following dopamine depletion and provide a basis for further study of its potential as a noninvasive, disease-modifying intervention for PD.

Identifiers

PMID41427361
PMCPMC12715545

What Socratic 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 Socratic graph.