Effective treatments for stroke and cerebral ischemia remain elusive. Strokes account for 10% of all premature deaths with a poor prognosis for surviving patients. The extent of the brain injury and the potential for its reversal depend upon the degree and duration of the ischemia. Infarcted tissue cannot be rescued; however, efforts to prevent additional damage represent the focus of novel treatments. The progression and extent of the injury is dependent upon the role of invasive neutrophils and cytotoxic and inflammatory cytokines, the expression of which are under control of the transcription factor, NF-kB. Activation of NF-kB results from proteolysis of its inhibitory protein, IkBa, via the intracellular ubiquitin-proteasome pathway. Proteasome inhibitors would block NF-kB activation and potentially reduce ischemic injury by attenuating the expression of many cytokines and adhesion molecules. To address the utility of proteasome inhibitors in stroke, we propose their testing in rodents using the nylon-filament middle cerebral artery occlusion method of ischemia. Preliminary in vitro and in vivo evidence is provided to support this hypothesis. Additional data from our Phase I research plan would be used to support development (Phase II) of such compounds as an intravenous therapy for post-stroke victims.

Proposed Commercial Applications

The aim of the proposal is the further understanding and utilization of the proteasome inhibitor PS-5 19, that significantly reduces ischemic brain injury. We would develop this compound into an effective drug for treating post- stroke victims. This drug and its analogs could also have therapeutic utility in other disorders, including brain and spinal cord injury, cerebrovascular vasospasm, myocardial ischemia, neointimal hyperplasia, neurotrauma and restenosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43NS037292-01A1
Application #
2718010
Study Section
Special Emphasis Panel (ZRG1-NEUA (01))
Program Officer
Jacobs, Tom P
Project Start
1999-02-19
Project End
1999-08-18
Budget Start
1999-02-19
Budget End
1999-08-18
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Proscript, Inc.
Department
Type
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Steward, O; Schuman, E M (2001) Protein synthesis at synaptic sites on dendrites. Annu Rev Neurosci 24:299-325
Kantor, D B; Lanzrein, M; Stary, S J et al. (1996) A role for endothelial NO synthase in LTP revealed by adenovirus-mediated inhibition and rescue. Science 274:1744-8