Robust High-throughput Mechanical Phenotyping Platform for Clinical Diagnostics

Award Information
Agency: Department of Health and Human Services
Branch: N/A
Contract: 1R43NS084566-01
Agency Tracking Number: R43NS084566
Amount: $225,043.00
Phase: Phase I
Program: SBIR
Awards Year: 2013
Solicitation Year: 2013
Solicitation Topic Code: NINDS
Solicitation Number: PA12-088
Small Business Information
2802 Flintrock Trace, AUSTIN, TX, -
DUNS: 793502068
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 (214) 280-9677
Business Contact
Phone: (214) 280-9677
Research Institution
DESCRIPTION (provided by applicant): The Specific Aim of this proposal is to test the feasibility of using a novel method of enhancing neuroplasticity for the purpose of producing clinically significant improvements in the ability of stroke patients to perform their activities o daily living (ADLs). One of the major goals of MicroTransponder is to translate pre-clinical findings of enhancing neuroplasticity into clinical use to help rehabilitate people with neurological deficits. Our method of enhancing neuroplasticity is pairing very short pulses of vagus nerve stimulation (VNS) with specific therapeutic exercises. This method is a novel application of VNS that is sharply distinct from the current clinical use of VNS for the treatment of refractory epilepsy and depression. For treatment of epilepsy and depression, VNS is given 24 hours per day seven days a week and the stimulation is not paired with any specific input. For our treatment, there is specific pairing of VNS with a task to be learned and VNS isonly delivered while the patient is practicing the task. Ischemic stroke is a leading cause of adult disability in the US, with upper motor deficits being the primary cause of the disability. These disabilities prevent patients from performing ADLs, whichmakes them dependent on caregivers. This situation is associated with serious co-morbidities, including depression. In all, such patients suffer a serious loss in quality of life. Current rehabilitation techniques help some patients regain some degree of lost upper limb function; however, a much greater degree of recovery is still needed in order to allow patients to achieve the key goal of gaining independence. To address this unmet medical need, we are evaluating the method of pairing VNS with rehabilitative tasks in rat models of ischemic stroke. In preliminary findings using an endothelin-1 (ET-1) stroke model, we observed that VNS paired with an upper limb motor task resulted in full recovery of lost function, while rehabilitation without VNS generatedonly partial recovery with a sustained plateau of suboptimal function. However, there are several key issues that must still be addressed in order to support testing this method in stroke patients. We must show that VNS will generalize to more than one model of ischemic insult and that the results are long lasting. To achieve our Specific Aim, we will carry out the following Task: Task 1: Using a rat model of middle cerebral artery occlusion (MCAo), evaluate recovery of function of upper limb motor deficits in three groups of rats: Group 1: VNS paired with rehabilitation training, Group 2: VNS offset one hour before rehabilitation training (unpaired), and Group 3: VNS implant but no stimulation (sham control). We must find at least 80% greater recovery of function when VNS is paired with training than in the other groups. Further, recovery of function in animals that received VNS paired with training must maintain at least 90% of those gains for at least five weeks in the absence of subsequent training.PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: Project Narrative In the United States, there are about 700,000 cases of ischemic stroke each year, leaving hundreds of thousands of people without the ability to perform simple tasks in their daily lives. This is a proposal to develop a novel therapy to help such patients to recovery such lost abilities.

* information listed above is at the time of submission.

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