Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Wednesday, August 19, 2026

Motor imagery enhances swallowing motor cortex excitability and activates sensorimotor regions: a TMS and fNIRS study

 Will your competent? doctor bring this intervention into the hospital? NO? Why not? Although first they have to initiate research on stroke subjects.

Laziness? Incompetence? Or just don't care? NO leadership? NO strategy? Not my job? Not my Problem!

Motor imagery enhances swallowing motor cortex excitability and activates sensorimotor regions: a TMS and fNIRS study

    We’re sharing this article early to provide faster access to peer-reviewed, accepted research. It is citable and carries a permanent DOI. This version is subject to further edits and will be replaced automatically by the final Version of Record. All legal disclaimers apply.

    Abstract

    Background

    Action observation (AO) and motor imagery (MI) represent promising, non-invasive strategies for promoting neuroplasticity in motor rehabilitation by engaging the shared neural substrates of actual movement. However, their translation to swallowing rehabilitation, particularly for neurogenic dysphagia, lacks a robust neurophysiological foundation. A critical barrier is the absence of direct, multimodal evidence comparing how swallowing-specific static AO (SAO), dynamic AO (DAO), and MI differentially engage the cortical swallowing network. Specifically, their immediate effects on corticobulbar excitability and hemodynamic activation within key sensorimotor regions remain unquantified and poorly contrasted, limiting the rationale for their targeted clinical application.

    Objective

    This study employed a dual-modal neuroimaging approach to precisely quantify and compare the immediate neurophysiological effects of SAO, DAO, and MI on the human swallowing sensorimotor system. We aim to evaluate their modulatory effects on bilateral suprahyoid motor cortical excitability and intracortical inhibitory/facilitatory circuitry using transcranial magnetic stimulation (TMS), and map their hemodynamic activation patterns within core sensorimotor cortices compared to motor execution (ME) using functional near-infrared spectroscopy (fNIRS).

    Methods

    Thirty-two healthy adults underwent integrated assessments using transcranial magnetic stimulation (TMS) and functional near-infrared spectroscopy (fNIRS). TMS measured motor-evoked potentials (MEPs), short-interval intracortical inhibition (SICI), and intracortical facilitation (ICF) in bilateral suprahyoid motor cortices during rest, SAO, DAO, and MI. fNIRS mapped hemodynamic changes in dorsal/ventral precentral (dPreCG/vPreCG) and postcentral gyri (dPoCG/vPoCG), superior/middle frontal gyri (SFG/MFG) during swallowing-specific SAO, DAO, MI and ME.

    Results

    MI reduced bilateral SICI and increased left ICF, concurrently activating bilateral dPoCG, left SFG/MFG, and right dPreCG/vPreCG/vPoCG—regions overlapping with ME-activated networks (bilateral vPreCG/vPoCG/MFG), with left MFG, right vPreCG/vPoCG as coactivating areas. In contrast, DAO reduced left SICI but elicited no hemodynamic activation, while SAO showed no significant effects.

    Conclusion

    MI enhances the excitability of the swallowing motor cortex and activates the key sensorimotor cortical areas governed ME of swallowing. MI shows greater superiority over AO and may become a promising effective rehabilitation strategy for neurogenic dysphagia.

    Trial registration Chinese Clinical Trial Registry, ChiCTR2000036715. Registered on 24 August 2020, https//www.chictr.org.cn/bin/home.

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