Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2022 Jul 28:11:e81306.
doi: 10.7554/eLife.81306.

Connecting the lines after a stroke

Affiliations
Editorial

Connecting the lines after a stroke

S Thomas Carmichael. Elife. .

Abstract

In mice, stimulating cortical areas in the undamaged hemisphere of a brain affected by stroke impairs recovery.

Keywords: brain; functional connectivity; mouse; neuroscience; optogenetics; plasticity; stroke.

PubMed Disclaimer

Conflict of interest statement

SC No competing interests declared

Figures

Figure 1.
Figure 1.. Stimulating cortex areas contralateral to the site of a stroke impairs recovery and reconnection.
(A) Dorsal view of the human brain. Cortical areas in the human brain are functionally connected with regions in both the same (ipsilateral) and opposite (contralateral) hemisphere. These connections (represented by arrows) are present when brain areas are co-active in time and are associated with a behavioral output, such as moving or sensing the hand. (B) Dorsal view of the mouse brain. Stimulation of the mouse forepaw activates a specific region of the primary somatosensory cortex that the paw is mapped on to, which is the area studied by Bice et al. (C) Inducing a stroke in the forepaw area (red circle) stops the activation of this region and the surrounding cortex following forepaw stimulation for at least seven days. At later time points (one month), stimulation of the forepaw is once again able to activate the brain, this time in a forepaw representation that is shifted to a new site due to cortical plasticity. At later time points, the forepaw cortical area is re-integrated into a network in which it is connected to ipsilateral sensory, motor and cortical associated areas, and contralateral sensory and motor areas. (D) Chronic, daily stimulation of the somatosensory cortex that is contralateral to the stroke site (lightning bolt) impairs the local remapping of the forepaw area and interferes with the integration of the recovered cortex into functional brain networks. Under these conditions, callosal connections, when activated, actually inhibit large areas of the cortex in the opposite hemisphere.

Comment on

  • doi: 10.7554/eLife.68852

References

    1. Bice AR, Xiao Q, Kong J, Yan P, Rosenthal ZP, Kraft AW, Smith KP, Wieloch T, Lee JM, Culver JP, Bauer AQ. Homotopic contralesional excitation suppresses spontaneous circuit repair and global network reconnections following ischemic stroke. eLife. 2022;11:e68852. doi: 10.7554/eLife.68852. - DOI - PMC - PubMed
    1. Bowren M, Bruss J, Manzel K, Edwards D, Liu C, Corbetta M, Tranel D, Boes AD. Post-stroke outcomes predicted from multivariate lesion-behaviour and lesion network mapping. Brain. 2022;145:1338–1353. doi: 10.1093/brain/awac010. - DOI - PMC - PubMed
    1. Brown CE, Aminoltejari K, Erb H, Winship IR, Murphy TH. In vivo voltage-sensitive dye imaging in adult mice reveals that somatosensory maps lost to stroke are replaced over weeks by new structural and functional circuits with prolonged modes of activation within both the peri-infarct zone and distant sites. The Journal of Neuroscience. 2009;29:1719–1734. doi: 10.1523/JNEUROSCI.4249-08.2009. - DOI - PMC - PubMed
    1. Cheng MY, Wang EH, Woodson WJ, Wang S, Sun G, Lee AG, Arac A, Fenno LE, Deisseroth K, Steinberg GK. Optogenetic neuronal stimulation promotes functional recovery after stroke. PNAS. 2014;111:12913–12918. doi: 10.1073/pnas.1404109111. - DOI - PMC - PubMed
    1. Henrich-Noack P, Sergeeva EG, Sabel BA. Non-invasive electrical brain stimulation: from acute to late-stage treatment of central nervous system damage. Neural Regeneration Research. 2017;12:1590–1594. doi: 10.4103/1673-5374.217322. - DOI - PMC - PubMed

Publication types