Effects of Postinfarct Myelin-Associated Glycoprotein Antibody Treatment on Motor Recovery and Motor Map Plasticity in Squirrel Monkeys

Send out for more research on this and what the translational protocol would look like.
http://stroke.ahajournals.org/content/early/2015/04/30/STROKEAHA.114.008088.abstract?sid=ec499f51-44bc-4180-9fe6-0e74006f3dae

1. Scott Barbay, PhD,
2. Erik J. Plautz, PhD,
3. Elena Zoubina, PhD,
4. Shawn B. Frost, PhD,
5. Steven C. Cramer, MD and
6. Randolph J. Nudo, PhD

+ Author Affiliations

1. From the Department of Molecular and Integrative Physiology, Landon Center on Aging, University of Kansas Medical Center (S.B., E.J.P., E.Z., S.B.F., R.J.N.); and Department of Neurology and Department of Anatomy and Neurobiology, University of California, Irvine (S.C.C.).

+ Author Notes

• Current address for E.J.P.: Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas.
• Current address for E.Z.: Department of Neurology, Harvard Medical School, Boston, MA.

1. Correspondence to Randolph J. Nudo, PhD, University of Kansas Medical Center, Landon Center on Aging, MS 1005, 3901 Rainbow Blvd, Kansas City, KS 66160. E-mail rnudo@kumc.edu

Abstract

Background and Purpose—New insights into the brain’s ability to reorganize after injury are beginning to suggest novel restorative therapy targets. Potential therapies include pharmacological agents designed to promote axonal growth. The purpose of this study was to test the efficacy of one such drug, GSK249320, a monoclonal antibody that blocks the axon outgrowth inhibition molecule, myelin-associated glycoprotein, to facilitate recovery of motor skills in a nonhuman primate model of ischemic cortical damage.

Methods—Using a between-groups repeated-measures design, squirrel monkeys were randomized to 1 of 2 groups: an experimental group received intravenous GSK249320 beginning 24 hours after an ischemic infarct in motor cortex with repeated dosages given at 1-week intervals for 6 weeks and a control group received only the vehicle at matched time periods. The primary end point was a motor performance index based on a distal forelimb reach-and-retrieval task. Neurophysiological mapping techniques were used to determine changes in spared motor representations.

Results—All monkeys recovered to baseline motor performance levels by postinfarct day 16. Functional recovery in the experimental group was significantly facilitated on the primary end point, albeit using slower movements. At 7 weeks post infarct, motor maps in the spared ventral premotor cortex in the experimental group decreased in area compared with the control group.

Conclusions—GSK249320, initiated 24 hours after a focal cortical ischemic infarct, facilitated functional recovery. Together with the neurophysiological data, these results suggest that GSK249320 has a substantial biological effect on spared cortical tissue. However, its mechanisms of action may be widespread and not strictly limited to peri-infarct cortex and nearby premotor areas.