Evidence map›Paper›PMID 41760198›Full record

ArticleSheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi2026

[Fiber photometry-based analysis of transcranial magneto-acoustic electrical stimulation effects on synaptic plasticity in the hippocampal CA1 region of APP/PS1 mice].

Jinrui Mi, Shuai Zhang, Xiaochao Lu, Yihao Xu, Guizhi Xu

Abstract readEnglish Abstract
In one paragraph

Article in Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jinrui MiSchool of Health Sciences and Biomedical Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.
Shuai ZhangSchool of Health Sciences and Biomedical Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.
Xiaochao LuSchool of Health Sciences and Biomedical Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.
Yihao XuSchool of Health Sciences and Biomedical Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.
Guizhi XuSchool of Health Sciences and Biomedical Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcranial magneto-acoustic electrical stimulation (TMAES) is a non-invasive novel neuromodulation technique based on the magneto-acoustic coupling effect. In this study, we employed APP/PS1 transgenic mice as an experimental model, targeting the hippocampus. Cognitive function was assessed through behavioral tests, while neuronal morphology was examined using hematoxylin-eosin and Golgi staining. Additionally, fiber photometry was utilized to measure calcium transient intensity in the CA1 region. By investigating the effects of TMAES on synaptic plasticity in the hippocampus, we aimed to elucidate its potential regulatory mechanisms in improving cognitive function in AD mice. Behavioral results showed that the cognitive and memory abilities of mice in the AD+sham group were significantly lower than those in the WT+sham group, while TMAES intervention could significantly improve the cognitive function of mice in the AD+TMAES group. Morphological detection indicated that the number of pyramidal neurons and the density of dendritic spines in the hippocampal CA1 region of the AD+sham group were decreased, with an increased proportion of immature spines; all the above indicators were significantly improved after TMAES intervention. Fiber photometric detection revealed that the calcium activity and calcium amplitude of neurons in the CA1 region of the AD+TMAES group were significantly enhanced compared with those of the AD+sham group. Pearson correlation analysis showed that cognitive level was positively correlated with calcium amplitude, dendritic spine density, and mature spine proportion. Meanwhile, calcium amplitude was positively correlated with dendritic spine density and mature spine proportion. Therefore, TMAES may alleviate the damage to synaptic plasticity in the hippocampal CA1 region of APP/PS1 mice by regulating the function of calcium ion channels, thereby improving cognitive impairment.

Indexed as

Alzheimer DiseaseCA1 Region, HippocampalNeuronal PlasticityTranscranial Direct Current StimulationAcoustic StimulationAmyloid beta-Protein PrecursorAnimalsMaleMiceMice, TransgenicPhotometryPresenilin-1Amyloid beta-Protein PrecursorPresenilin-1APP/PS1 miceCalcium activityHippocampal CA1 regionSynaptic plasticityTranscranial magneto-acoustic electrical stimulation

Identifiers

PMID41760198
PMCPMC12948546

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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.