Evidence map›Paper›PMID 40682580›Full record

ArticleNeuromodulation : journal of the International Neuromodulation Society2026

Cerebral Blood Flow Responses to Extracranial Alternating Current Brain Stimulation in CVN Mouse Model of Alzheimer's Disease: A Pilot Study Determining Optimal Dose.

Simone Degan, Yu Feng, Carol Colton, Stephen Schmidt, Angel V Peterchev, Dennis A Turner

Abstract read
In one paragraph

Article in Neuromodulation : journal of the International Neuromodulation Society, 2026. 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

6 authors.

Simone DeganNeurosurgery, Duke University Medical Center, Durham, NC, USA; Research and Surgery Services, Durham VA Medical Center, Durham, NC, USA.
Yu FengNeurosurgery, Duke University Medical Center, Durham, NC, USA.
Carol ColtonNeurology, Duke University Medical Center, Durham, NC, USA.
Stephen SchmidtNeurosurgery, Duke University Medical Center, Durham, NC, USA; Biomedical Engineering, Duke University Medical Center, Durham, NC, USA.
Angel V PeterchevNeurosurgery, Duke University Medical Center, Durham, NC, USA; Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA; Biomedical Engineering, Duke University Medical Center, Durham, NC, USA; Electrical and Computer Engineering, Duke University, Durham, NC, USA.
Dennis A TurnerNeurosurgery, Duke University Medical Center, Durham, NC, USA; Biomedical Engineering, Duke University Medical Center, Durham, NC, USA; Neurobiology, Duke University Medical Center, Durham, NC, USA; Research and Surgery Services, Durham VA Medical Center, Durham, NC, USA. Electronic address: dennis.turner@duke.edu.

Funding

Hypoperfusion, Hemodynamic Control Domains and Neurovascular Dysregulation in AD brain pathologyR01AG081774 · NIA · DUKE UNIVERSITY · PI DENNIS Alan TURNER · 2023 to 2026
$1.9M
Extracranial Brain Stimulation Reduces Metabolic Insufficiency Through Enhanced Cerebral Blood Flow in CVN-AD Alzheimer's ModelR01AG074999 · NIA · DUKE UNIVERSITY · PI TURNER, DENNIS ALAN · 2022 to 2025
$1.5M
Hippocampal Neurovascular Plasticity in CVN-AD Mouse: Fornix-Septal StimulationR21AG051103 · NIA · DUKE UNIVERSITY · PI TURNER, DENNIS ALAN · 2016 to 2017
$423k
BLRD VA I21 BX003023NIA NIH HHS R01 AG074999NIA NIH HHS R01 AG081774NIA NIH HHS R21 AG051103RRD VA I21 RX002223RRD VA I21 RX004081
6 · The paper itself

Abstract

introductionInsufficient metabolic supply in response to neural demand is a key mechanism of degeneration in Alzheimer's disease [AD]. However, extracranial alternating current [AC] stimulation can increase cerebral blood flow [CBF] and metabolic substrate supply to the brain. In this work, we investigate in an initial, pilot study the optimal dosage of extracranial AC brain stimulation appropriate for long-term treatment to retard degeneration in a mouse AD model [CVN]. MATERIALS AND

methodsWe applied extracranial AC (0.5-2.0 mA; 10 Hz; 20-second bursts) to CVN and control C57Bl/6 mice while measuring CBF and intracerebral electric field in vivo in anesthetized animals, and behavioral responses in awake animals.

resultsWe found a significant, diffuse increase in cortical CBF (2.6% increase at 0.75 mA) and intracerebral electric field (6.36mV/mm gradient at 0.75 mA) in response to extracranial AC brain stimulation in both CVN and control mice. In awake, behaving mice, the optimal dose of stimulation was 0.75 mA (in 30-second bursts), causing no adverse behavioral effects.

conclusionScheduled (at fixed times) or demand-triggered (during dynamic metabolic need) bursts of extracranial brain stimulation could enhance CBF to improve brain metabolic supply. The goal of this potential AD treatment is to alleviate mismatches between neural metabolic demand and brain substrate supply, to prevent AD phenotypic disease progression. Based on these pilot data, 0.75 mA is an optimal stimulation treatment dose leading to an appreciable net change in CBF, at a moderate intracranial electrical field, while also indicating behavioral tolerability, now being implemented in a long-term treatment trial.

Indexed as

Alzheimer DiseaseBrainCerebrovascular CirculationElectric Stimulation TherapyAmyloid beta-Protein PrecursorAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLMice, TransgenicPilot ProjectsAmyloid beta-Protein PrecursorAlzheimer's diseasecerebral blood flowelectric fieldextracranial brain stimulation

Identifiers

PMID40682580
PMCPMC12313132

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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.