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Matthew Bruce

Principal Scientist/Engineer

Email

mbruce@apl.washington.edu

Phone

206-685-2283

Education

B.S. Electrical and Computer Engineering, Michigan Technological University, 1991

M.S. Electrical and Computer Engineering, Virginia Polytechnic University, 1993

Ph.D. Bioengineering, University of Washington, 2004

Matthew Bruce's Website

http://staff.washington.edu/mbruce

Publications

2000-present and while at APL-UW

Glibenclamide treatment improved intraspinal blood volume, tissue sparing, and functional recovery after cervical spinal cord injury in rats

Prasse, T., and 11 others including M.F. Bruce, "Glibenclamide treatment improved intraspinal blood volume, tissue sparing, and functional recovery after cervical spinal cord injury in rats," Brain Res. Bull., 246, doi:10.1016/j.brainresbull.2026.112162, 2026.

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1 Nov 2026

Limiting the expansion of the primary injury after a traumatic spinal cord injury (SCI) can offer improved functional outcomes. Glibenclamide (glyburide) has been shown to limit intraspinal bleeding and promote vascular stability after SCI in rats, but its impact on intraspinal hemodynamics has not been investigated. Here, we hypothesized that acute glibenclamide treatment would improve intraspinal hemodynamics after a cervical contusion SCI in a rat model (200 kdyn). Intravital ultrafast contrast-enhanced ultrasound (CEUS) imaging revealed that glibenclamide treatment significantly increased total blood volume (i.e., tissue perfusion) at 72-hours post-injury (hpi) compared to vehicle treated controls (p < 0.05, Cohen's d >1.2). Histological data confirmed that glibenclamide treatment significantly lowered caspase-8-positive cells in the white matter at 72-hpi (p < 0.05, Cohen's d>1.2). Weekly forelimb locomotor scoring revealed significant functional improvements in animals treated with glibenclamide at 4-weeks post-injury (wpi) (p < 0.001, Cohen's d>1.2), which continued through to 8-wpi compared to vehicle treated animals (p < 0.05, Cohen's d>1.2). Glibenclamide intervention significantly reduced lesion size by 8-wpi compared to controls (p < 0.05, Cohen's d>1.2). This study is the first to report in vivo improvements in intraspinal blood volume associated with glibenclamide treatment after acute cervical SCI in rats.

Contrast-enhanced ultrasound demonstrates a severity-dependent hemodynamic response to acute dural decompression in concussive rodent spinal cord injury

Ramkumar, R., and 7 others including M.F. Bruce, "Contrast-enhanced ultrasound demonstrates a severity-dependent hemodynamic response to acute dural decompression in concussive rodent spinal cord injury," Neurotrauma Rep., 7, doi:10.1177/2689288X261479412, 2026.

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25 Aug 2026

Traumatic spinal cord injury (tSCI) is characterized by early microvascular disruption and regional perfusion failure that contribute to secondary tissue loss. The physiological effects of early decompression on spinal cord perfusion across injury severities remain incompletely defined. This study examined the influence of injury severity on perfusion dynamics and the impact of durotomy using contrast-enhanced ultrasound (CEUS) in a rat model of tSCI. Female Long–Evans rats underwent contusive injuries of graded severity (100, 150, 200 kDyn) at the T8 level, followed by decompressive durotomy or no further intervention. CEUS was performed at baseline, immediately after injury, 1 and 24 h postinjury to derive spatially resolved perfusion metrics, including normalized area under the curve (AUC) and spinal perfusion index (SPI). Perfusion was analyzed across defined regions: injury center, perilesional transition zone, and distal spinal cord. Functional recovery was assessed longitudinally using Basso, Beattie, and Bresnahan locomotor scoring and ladder walk testing, and spared myelin was quantified histologically at 8 weeks postinjury (wpi). Contusive tSCI produced an immediate, severity-dependent reduction in spinal cord perfusion at the lesion epicenter, with progressive involvement of adjacent segments at higher injury severities. Decompressive durotomy selectively improved perilesional perfusion following moderate injury (150 kDyn), reflected by a higher SPI (0.49 vs. 0.30, p = 0.005) and a concordant increase in perilesional AUC at 1 h. These perfusion changes were spatially restricted and transient. In exploratory analyses of chronic outcomes, moderate-injury cohort showed focal, nonsignificant trends toward greater perilesional myelin preservation and improved motor performance; total spared white matter and locomotor scores did not differ significantly between groups. These findings demonstrate that the perfusion benefits of early decompression are severity-dependent, with maximal effects in perilesional tissue following moderate injury. Quantitative CEUS provides a physiologically grounded approach for assessing therapeutic responsiveness in acute tSCI and may help guide optimization of decompressive strategies.

Sound decisions: real-time ultrasound in the management of traumatic spinal cord injury

Hofstetter, C.P., A. Sadeghi, R. Ramkumar, M. Bruce, and Z.Z. Khaing, "Sound decisions: real-time ultrasound in the management of traumatic spinal cord injury," Curr. Opin. Neurobiol., 38, 635-643, doi:10.1097/WCO.0000000000001432, 2025.

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1 Dec 2025

Traumatic spinal cord injury (tSCI) is a devastating neurological emergency with high morbidity and no proven therapies that reliably improve recovery. While early decompression and hemodynamic optimization are standard, clinicians lack imaging tools to stratify injury severity or monitor physiological responses in real time. Advances in high-resolution B-mode, contrast-enhanced ultrasound, and multiparametric approaches offer a unique opportunity to close this gap and improve patient-specific treatment strategies.

More Publications

Acoustics Air-Sea Interaction & Remote Sensing Center for Industrial & Medical Ultrasound Electronic & Photonic Systems Environmental & Information Systems Ocean Engineering Ocean Physics Polar Science Center
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