» Articles » PMID: 22829873

Imaging the Spatio-temporal Dynamics of Supragranular Activity in the Rat Somatosensory Cortex in Response to Stimulation of the Paws

Overview
Journal PLoS One
Date 2012 Jul 26
PMID 22829873
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

We employed voltage-sensitive dye (VSD) imaging to investigate the spatio-temporal dynamics of the responses of the supragranular somatosensory cortex to stimulation of the four paws in urethane-anesthetized rats. We obtained the following main results. (1) Stimulation of the contralateral forepaw evoked VSD responses with greater amplitude and smaller latency than stimulation of the contralateral hindpaw, and ipsilateral VSD responses had a lower amplitude and greater latency than contralateral responses. (2) While the contralateral stimulation initially activated only one focus, the ipsilateral stimulation initially activated two foci: one focus was typically medial to the focus activated by contralateral stimulation and was stereotaxically localized in the motor cortex; the other focus was typically posterior to the focus activated by contralateral stimulation and was stereotaxically localized in the somatosensory cortex. (3) Forepaw and hindpaw somatosensory stimuli activated large areas of the sensorimotor cortex, well beyond the forepaw and hindpaw somatosensory areas of classical somatotopic maps, and forepaw stimuli activated larger cortical areas with greater activation velocity than hindpaw stimuli. (4) Stimulation of the forepaw and hindpaw evoked different cortical activation dynamics: forepaw responses displayed a clear medial directionality, whereas hindpaw responses were much more uniform in all directions. In conclusion, this work offers a complete spatio-temporal map of the supragranular VSD cortical activation in response to stimulation of the paws, showing important somatotopic differences between contralateral and ipsilateral maps as well as differences in the spatio-temporal activation dynamics in response to forepaw and hindpaw stimuli.

Citing Articles

Anesthetic modulations dissociate neuroelectric characteristics between sensory-evoked and spontaneous activities across bilateral rat somatosensory cortical laminae.

Baek K, Park C, Jang S, Shim W, Ro Kim Y Sci Rep. 2022; 12(1):11661.

PMID: 35804171 PMC: 9270342. DOI: 10.1038/s41598-022-13759-0.


Cortical layer-specific modulation of neuronal activity after sensory deprivation due to spinal cord injury.

Zaforas M, Rosa J, Alonso-Calvino E, Fernandez-Lopez E, Miguel-Quesada C, Oliviero A J Physiol. 2021; 599(20):4643-4669.

PMID: 34418097 PMC: 9292026. DOI: 10.1113/JP281901.


Hindlimb Somatosensory Information Influences Trunk Sensory and Motor Cortices to Support Trunk Stabilization.

Nandakumar B, Blumenthal G, Pauzin F, Moxon K Cereb Cortex. 2021; 31(11):5165-5187.

PMID: 34165153 PMC: 8491683. DOI: 10.1093/cercor/bhab150.


Distinct patterns of activity in individual cortical neurons and local networks in primary somatosensory cortex of mice evoked by square-wave mechanical limb stimulation.

Bandet M, Dong B, Winship I PLoS One. 2021; 16(4):e0236684.

PMID: 33914738 PMC: 8084136. DOI: 10.1371/journal.pone.0236684.


Monitoring of Stimulus Evoked Murine Somatosensory Cortex Hemodynamic Activity With Volumetric Multi-Spectral Optoacoustic Tomography.

Larney B, Hutter M, Degtyaruk O, Dean-Ben X, Razansky D Front Neurosci. 2020; 14:536.

PMID: 32581686 PMC: 7283916. DOI: 10.3389/fnins.2020.00536.


References
1.
Yu X, Wang S, Chen D, Dodd S, Goloshevsky A, Koretsky A . 3D mapping of somatotopic reorganization with small animal functional MRI. Neuroimage. 2009; 49(2):1667-76. PMC: 2967485. DOI: 10.1016/j.neuroimage.2009.09.021. View

2.
Shuler M, Krupa D, Nicolelis M . Bilateral integration of whisker information in the primary somatosensory cortex of rats. J Neurosci. 2001; 21(14):5251-61. PMC: 6762838. View

3.
Moxon K, Hale L, Aguilar J, Foffani G . Responses of infragranular neurons in the rat primary somatosensory cortex to forepaw and hindpaw tactile stimuli. Neuroscience. 2008; 156(4):1083-92. DOI: 10.1016/j.neuroscience.2008.08.009. View

4.
Usunoff K, Kharazia V, Valtschanoff J, Schmidt H, Weinberg R . Nitric oxide synthase-containing projections to the ventrobasal thalamus in the rat. Anat Embryol (Berl). 1999; 200(3):265-81. DOI: 10.1007/s004290050278. View

5.
Mohajerani M, Aminoltejari K, Murphy T . Targeted mini-strokes produce changes in interhemispheric sensory signal processing that are indicative of disinhibition within minutes. Proc Natl Acad Sci U S A. 2011; 108(22):E183-91. PMC: 3107306. DOI: 10.1073/pnas.1101914108. View