Simulations of spinal cord recruitment to optimize bioelectronic interventions for lower urinary tract control

NIH RePORTER · NIH · OT2 · $753,687 · view on reporter.nih.gov ↗

Abstract

Lower urinary tract (LUT) dysfunction occurs in 20-40% of the global population and has an economic impact measured in tens of billions of dollars every year in the United States. This field desperately needs new therapies as current treatments, such as clean intermittent catheterization and pharmaceuticals, have significant side effects. Epidural spinal cord stimulation (SCS) provides a potential solution. SCS is a rapidly growing area of bioelectronic medicine, with tens of thousands of implants occurring each year in the United States. While SCS normally activates the dorsal columns, this technique can also be used to recruit primary sensory neurons as they enter the spinal cord through the dorsal rootlets. These sensory inputs play a crucial role in regulating bladder function6 and activating these primary sensory neurons can have powerful effects on bladder behavior. Through ongoing SPARC efforts, our team has established that high-resolution SCS can selectively recruit sacral afferents leading to both micturition and continence reflexes. These data support our ultimate translational goal to develop a SGS therapy to improve bladder function after injury and disease. However, a critical gap remains to understand, develop and optimize these neuromodulation therapies. There are no models that accurately represent the complex sacral spinal anatomy, and previous modelling efforts have consistently ignored the dorsal rootlets. In this project, we will develop functionalized, anatomically accurate models of the cat sacral spinal cord. including the dorsal rootlets, and validate these models using electrophysioloqical data acquired under an existing SPARC effort. Task 1: Create a pipeline for anatomically accurate, ultra-high resolution finite element models of the cat sacral spinal cord Accurate anatomy is critical for biophysical models of stimulation-evoked neural recruitment. However, these structures have been underappreciated in modelling efforts, in part due to their anatomical complexity. We will use diffusion tensor imaging (DTI) and structural magnetic resonance imaging to acquire detailed anatomy of the sacral spinal cord in the cat, including dorsal and ventral rootlet fiber pathways and develop a pipeline within o2S2PARC segment these images and create finite element method (FEM) models of these tissues. Year 1: Imaging dataset of sacral spinal cord in one cat and preliminary pipeline. Year 2: Imaging datasets for four spinal cords to validate anatomical model creation pipeline. Task 2: Create finite element models, functionalized with computational axon models, and validate recruitment using existing electrophysiological data We will use Sim4Life and the o2S2PARC platform to mesh and populate simplified and anatomically accurate spinal cord models with populations of pelvic, pudenda! and sciatic nerve axons that project into the cord. DTI data will be used to create realistic 3D axon trajectories and the model will be validated using e...

Key facts

NIH application ID
10469840
Project number
3OT2OD030537-01S1
Recipient
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
Principal Investigator
Robert A Gaunt
Activity code
OT2
Funding institute
NIH
Fiscal year
2021
Award amount
$753,687
Award type
3
Project period
2020-09-15 → 2023-05-31