Accession Number:

ADA621845

Title:

Advanced Restoration Therapies in Spinal Cord Injury

Descriptive Note:

Annual rept. 15 Apr 2014-14 Apr 2015

Corporate Author:

KENNEDY KRIEGER INST INC BALTIMORE MD HUGO W MOSER RESEARCH INST

Personal Author(s):

Report Date:

2015-07-01

Pagination or Media Count:

18.0

Abstract:

Evidence suggests that functional electrical stimulation FES can improve the function of the central nervous system CNS after injury or disease. Using FES-based therapies to treat spinal cord injured patients in our clinic, we have observed neurological and physical improvements. Investigations in our basic science research laboratory address the mechanisms by which FES promotes the cellular and molecular CNS regeneration that forms the foundations of this recovery.. SPECIFIC AIM 1 Determine if functional electrical stimulation FES in a mouse model of chronic spinal cord injury SCI induces proliferation and differentiation of genetically labeled oligodendrocyte progenitor cells OPCs Months 1-12. SPECIFIC AIM 2 Determine if FES induces remyelination by mature oligodendrocytes in a mouse model of chronic SCI Months 1-24. SPECIFIC AIM 3 Determine if functional electrical stimulation in a mouse model of chronic SCI induces cortical plasticity as measured by resting state functional magnetic resonance imaging rs-fMRI Months 1-24. Relevance The studies proposed will continue to investigate the role of FES-based restorative therapies in promoting neurological and functional recovery in chronic SCI. We will use existing transgenic mouse lines that enable the genetically labeling of cellular populations to further our understanding of the mechanisms through which FES induces functional recovery. Additionally, we will use a newly developed transgenic mouse lines that enables us to examine the dynamics of myelin formation. We will also further our imaging work by developing methodology to use rs-fMRI for examination of cortical plasticity in response to FES.

Subject Categories:

  • Anatomy and Physiology
  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE