Subcutaneous tri‐block copolymer produces recovery from spinal cord injury
- 5 March 2004
- journal article
- research article
- Published by Wiley in Journal of Neuroscience Research
- Vol. 76 (1) , 141-154
- https://doi.org/10.1002/jnr.20053
Abstract
We have studied the ability of nonionic detergents and hydrophilic polymers to seal permeabilized membranes of damaged cells, rescuing them from progressive dissolution, degeneration, and death. We report that a single subcutaneous injection of the tri-block copolymer, Poloxamer 188 (P188) 6 hr after a severe compression of the adult guinea pig spinal cord is able to: (1) preserve the anatomic integrity of the cord; (2) produce a rapid recovery of nerve impulse conduction through the lesion; and (3) produce a behavioral recovery of a spinal cord dependent long tract spinal cord reflex. These observations stood out against a control group in blinded evaluation. Conduction through the lesion was monitored by stimulating the tibial nerve of the hind limb, and measuring the arrival of evoked potentials at the contralateral sensory cortex of the brain (somatosensory evoked potentials; SSEP). Behavioral recovery was determined by a return of sensitivity of formerly areflexic receptive fields of the cutaneous trunchi muscle (CTM) reflex. This contraction of back skin in response to tactile stimulation is totally dependent on the integrity of an identified bilateral column of ascending long tract axons. A statistically significant recovery of both SSEP conduction through the lesion and the CTM reflex occurred in P188-treated animals compared to vehicle-treated controls. Quantitative 3D computer reconstruction of the lesioned vertebral segment of spinal cord revealed a statistically significant sparing of spinal cord parenchyma and a significant reduction in cavitation of the spinal cord compared to control animals We determined that the proportion of P188-treated animals that recovered evoked potentials were nearly identical to that produced by a subcutaneous injection of polyethylene glycol (PEG). In contrast, P188 was not as effective as PEG in producing a recovery of CTM functioning. We discuss the likely differences in the mechanisms of action of these two polymers, and the possibilities inherent in a combined treatment.Keywords
This publication has 41 references indexed in Scilit:
- Polyethylene Glycol Rapidly Restores Physiological Functions in Damaged Sciatic Nerves of Guinea PigsNeurosurgery, 2002
- Cellular Engineering: Molecular Repair of Membranes to Rescue Cells of the Damaged Nervous SystemNeurosurgery, 2001
- Amphiphilic, tri-block copolymers provide potent membrane-targeted neuroprotectionThe FASEB Journal, 2001
- Human Spinal Cord Retains Substantial Structural Mass in Chronic Stages After InjuryJournal of Neurotrauma, 1999
- Evolution of Lipidic Structures during Model Membrane Fusion and the Relation of This Process to Cell Membrane FusionBiochemistry, 1997
- Promising Therapy for Cell Membrane DamageAnnals of the New York Academy of Sciences, 1994
- The neuroprotective pharmacology of methylprednisoloneJournal of Neurosurgery, 1992
- Cutaneus trunci muscle reflex of the guinea pigJournal of Comparative Neurology, 1990
- Functional recovery after spinal cord hemisection in guinea pigs: The effects of applied electric fieldsJournal of Comparative Neurology, 1990
- Behavioral Recovery Induced by Applied Electric Fields After Spinal Cord Hemisection in Guinea PigScience, 1987