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Willoughby, W. R.

Publications and source records attributed to Willoughby, W. R..

2 recordsLinked to original sources

Somatotopic Arrangement of Eight Distinct Skin Areas in the Human Primary Somatosensory Cortex Derived from Functional Magnetic Resonance Imaging

AO_SCPLOWBSTRACTC_SCPLOWBlood oxygen level dependent (BOLD) functional magnetic resonance imaging (fMRI) was used to investigate cortical activity associated with peripheral tactile stimuli in a small cohort of healthy humans. MR-safe automated pneumatic stimulators modeled after the Wartenberg pinwheel were used to generate tactile stimuli at regular intervals on eight disparate areas of skin. The phase-encoded BOLD responses of voxels in the cerebral cortex were characterized by the maximal normalized cross-correlation coefficients at time delays between an idealized response and the measure time course. Overall at the group level, the somatotopic organization of the somatosensory cortex (SI) follows the accepted homunculus model, but a noticeable amount of variation was observed between individual study participants. The surface areas of cortical regions in SI activated by tactile stimulation of different body parts were calculated, giving an estimate of cortical magnification factors. Data collected with the participant actively attending the stimuli were compared to data collected before the attention task. No significant attention-related changes were observed in the somatotopic maps or in time courses of voxels well-correlated to stimuli.

neuroscience↗

Localized delivery and uncaging of glutamate from MRI-visible albumin nanoclusters in the rat hippocampus using focused ultrasound

There is an ongoing need for noninvasive tools to manipulate brain activity with molecular, spatial and temporal specificity. Here we have investigated the use of MRI-visible, albumin-based nanoclusters for noninvasive, localized and temporally specific drug delivery to the rat brain. We demonstrated that IV injected nanoclusters could be deposited into target brain regions via focused ultrasound facilitated blood brain barrier opening. We showed that nanocluster location could be confirmed in vivo with MRI. Additionally, following confirmation of nanocluster delivery, release of the nanocluster payload into brain tissue can be triggered by a second focused ultrasound treatment performed without circulating microbubbles. Release of glutamate from nanoclusters in vivo caused enhanced c-Fos expression, indicating that the loading capacity of the nanoclusters is sufficient to induce neuronal activation. This novel technique for noninvasive stereotactic drug delivery to the brain with temporal specificity could provide a new way to study brain circuits in vivo preclinically with high relevance for clinical translation. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=36 SRC="FIGDIR/small/696237v4_ufig1.gif" ALT="Figure 1"> View larger version (16K): org.highwire.dtl.DTLVardef@b528f9org.highwire.dtl.DTLVardef@1950228org.highwire.dtl.DTLVardef@1c0ada0org.highwire.dtl.DTLVardef@c71790_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗