Literature DB >> 11818407

Behavioral recovery from spinal cord injury following delayed application of polyethylene glycol.

Richard B Borgens1, Riyi Shi, Debra Bohnert.   

Abstract

Topical application of the hydrophilic polymer polyethylene glycol (PEG) to isolated adult guinea pig spinal cord injuries has been shown to lead to the recovery of both the anatomical integrity of the tissue and the conduction of nerve impulses through the lesion. Furthermore, a brief (2 min) application of the fusogen (M(r) 1800, 50 % w/v aqueous solution) to the exposed spinal cord injury in vivo can also cause rapid recovery of nerve impulse conduction through the lesion in association with functional recovery. Behavioral recovery was demonstrated using a long-tract, spinal-cord-dependent behavior in rodents known as the cutaneus trunci muscle (CTM) reflex. This reflex is observed as a contraction of the skin of the back in response to tactile stimulation. Here, we confirm and extend these preliminary observations. A severe compression/contusion injury to the exposed thoracic spinal cord of the guinea pig was performed between thoracic vertebrae 10 and 11. Approximately 7 h later, a topical application of PEG was made to the injury (dura removed) for 2 min in 15 experimental animals, and levels of recovery were compared with those of 13 vehicle-treated control animals. In PEG-treated animals, 93 % recovered variable levels of CTM functioning and all recovered some level of conduction through the lesion, as measured by evoked potential techniques. The recovered reflex was relatively normal compared with the quantitative characteristics of the reflex prior to injury with respect to the direction, distance and velocity of skin contraction. Only 23 % of the control population showed any spontaneous CTM recovery (P=0.0003) and none recovered conduction through the lesion during the 1 month period of observation (P=0.0001). These results suggest that repair of nerve membranes by polymeric sealing can provide a novel means for the rapid restoration of function following spinal cord injury.

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Year:  2002        PMID: 11818407     DOI: 10.1242/jeb.205.1.1

Source DB:  PubMed          Journal:  J Exp Biol        ISSN: 0022-0949            Impact factor:   3.312


  31 in total

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Review 4.  Biomaterial design strategies for the treatment of spinal cord injuries.

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7.  Accumulation of acrolein-protein adducts after traumatic spinal cord injury.

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8.  Neuroprotective ferulic acid (FA)-glycol chitosan (GC) nanoparticles for functional restoration of traumatically injured spinal cord.

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Review 9.  A systematic review of non-invasive pharmacologic neuroprotective treatments for acute spinal cord injury.

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Review 10.  Role of electrical stimulation for rehabilitation and regeneration after spinal cord injury: an overview.

Authors:  Samar Hamid; Ray Hayek
Journal:  Eur Spine J       Date:  2008-08-02       Impact factor: 3.134

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