Intraspinal grafting procedures: Spinal cord effects induced in the adult rat: A clinical, histopathological, and immunohistochemical study

Objective: Intraspinal grafting procedures using peripheral nerve grafts (PNG) or collagen guidance channels (CGC) have been recently used to treat brachial plexus injuries in humans and spinal cord injuries in animals. This study examined the effects of these procedures in the adult rat. Methods: In adult rats, we performed an avulsion of left C5, C6, and C7 nerve roots, followed by a myelotomy of the left ventrolateral aspect of the spinal cord between C5 and C6. The rats were subsequently assigned to one of three groups: group A (n = 10), no additional procedure; group B (n = 10), implantation of a PNG following myelotomy; group C (n = 10), implantation of a CGC. Clinical evaluation was postoperatively assessed. Rats were euthanized at day 6 or 21. Spinal cord lesions induced by surgery were assessed by measuring depth and rostrocaudal extent. Reactive astrogliosis, as a reaction to neuroglial damage, was assessed by revealing the glial fibrillary acidic protein with immunochemistry method. Results: No animal showed persistent neurological deficit at day 21. The depth and rostrocaudal extent of tissue damage was comparable in all groups at days 6 and 21. At day 6, the astrocytic reaction observed at the myelotomy/implantation site was statistically stronger in group C (CGC). At day 21, the astrocytic reaction became identical in all groups. Conclusion: This study shows that grafting a PNG or a CGC into the spinal cord does not create significant additional iatrogenic effects and can be used in repair strategies to treat nerve root avulsions or spinal cord injuries. © 2006 Wiley‐Liss, Inc. Microsurgery, 2006.

[1]  M. Tadié,et al.  Experimental bypass surgery between the spinal cord and caudal nerve roots for spinal cord injuries. , 2004, Neuro-Chirurgie.

[2]  C. Brosnan,et al.  Quantitative aspects of reactive gliosis: A review , 1992, Neurochemical Research.

[3]  P. Guiheneuc,et al.  Partial return of motor function in paralyzed legs after surgical bypass of the lesion site by nerve autografts three years after spinal cord injury. , 2002, Journal of neurotrauma.

[4]  M. Tadié,et al.  Regeneration of primary sensory axons into the adult rat spinal cord via a peripheral nerve graft bridging the lumbar dorsal roots to the dorsal column , 2002, Journal of neuroscience research.

[5]  M. Tadié,et al.  Regrowth of the Rostral Spinal Axons into the Caudal Ventral Roots through a Collagen Tube Implanted into Hemisected Adult Rat Spinal Cord , 2001, Neurosurgery.

[6]  M. Tadié,et al.  Innervation of the caudal denervated ventral roots and their target muscles by the rostral spinal motoneurons after implanting a nerve autograft in spinal cord-injured adult marmosets. , 2001, Journal of neurosurgery.

[7]  M. Tadié,et al.  Horseradish peroxidase retrograde labeling of primary sensory neurons: A comparison of four intraspinal applicaton methods , 2001, Microsurgery.

[8]  T. Carlstedt,et al.  Spinal nerve root repair and reimplantation of avulsed ventral roots into the spinal cord after brachial plexus injury. , 2000, Journal of neurosurgery.

[9]  M R Gaab,et al.  Analysis of aqueductal cerebrospinal fluid flow after endoscopic aqueductoplasty by using cine phase-contrast magnetic resonance imaging. , 2000, Journal of neurosurgery.

[10]  C. Lacroix,et al.  Reinnervation of denervated lumbar ventral roots and their target muscle by thoracic spinal motoneurons via an implanted nerve autograft in adult rats after spinal cord injury , 1999, Journal of neuroscience research.

[11]  S. Cullheim,et al.  Nerve Growth Factor Induces Process Formation in Meningeal Cells: Implications for Scar Formation in the Injured CNS , 1998, The Journal of Neuroscience.

[12]  Charles Tator Biology of neurological recovery and functional restoration after spinal cord injury. , 1998, Neurosurgery.

[13]  M. Tadié,et al.  Axonal regrowth through a collagen guidance channel bridging spinal cord to the avulsed C6 roots: Functional recovery in primates with brachial plexus injury , 1998, Journal of neuroscience research.

[14]  M. Tadié,et al.  Strong expression of GFAP mRNA in rat hippocampus after a closed‐head injury , 1997, Neuroreport.

[15]  M. Tadié,et al.  Axonal regrowth through collagen tubes bridging the spinal cord to nerve roots , 1997, Journal of neuroscience research.

[16]  E. Sundström,et al.  Motor Performance Score: A New Algorithm for Accurate Behavioral Testing of Spinal Cord Injury in Rats , 1996, Experimental Neurology.

[17]  T. Carlstedt,et al.  Return of function after spinal cord implantation of avulsed spinal nerve roots , 1995, The Lancet.

[18]  Charles Tator Update on the Pathophysiology and Pathology of Acute Spinal Cord Injury , 1995, Brain pathology.

[19]  J. Wolff,et al.  Postnatal development of glial fibrillary acidic protein, vimentin and S100 protein in monkey visual cortex: evidence for a transient reduction of GFAP immunoreactivity. , 1994, Brain research. Developmental brain research.

[20]  Didier Orsal,et al.  Median nerve neurotization by peripheral nerve grafts directly implanted into the spinal cord: anatomical, behavioural and electrophysiological evidences of sensorimotor recovery , 1994, Brain Research.

[21]  D. Montgomery,et al.  Astrocytes: Form, Functions, and Roles in Disease , 1994, Veterinary pathology.

[22]  T. Carlstedt,et al.  Functional recovery in primates with brachial plexus injury after spinal cord implantation of avulsed ventral roots. , 1993, Journal of neurology, neurosurgery, and psychiatry.

[23]  J. O'Callaghan Quantitative Features of Reactive Gliosis following Toxicant‐induced Damage of the CNS a , 1993, Annals of the New York Academy of Sciences.

[24]  M. Ghandour,et al.  Double‐labeling in situ hybridization analysis of mRNAs for carbonic anhydrase II and myelin basic protein: Expression in developing cultured glial cells , 1991, Glia.

[25]  M. Hatten,et al.  Astroglia in CNS injury , 1991, Glia.

[26]  G. Moonen,et al.  Neurono-glial interactions and neural plasticity. , 1990, Progress in brain research.

[27]  S. Cullheim,et al.  Reinnervation of hind limb muscles after ventral root avulsion and implantation in the lumbar spinal cord of the adult rat. , 1986, Acta physiologica Scandinavica.

[28]  P. Reier GLIOSIS FOLLOWING CNS INJURY: THE ANATOMY OF ASTROCYTIC SCARS AND THEIR INFLUENCES ON AXONAL ELONGATION , 1986 .

[29]  L. Eng Glial fibrillary acidic protein (GFAP): the major protein of glial intermediate filaments in differentiated astrocytes , 1985, Journal of Neuroimmunology.

[30]  M. Berry,et al.  Observations on the astrocyte response to a cerebral stab wound in adult rats , 1985, Brain Research.

[31]  Ludwin Sk Reaction of oligodendrocytes and astrocytes to trauma and implantation. A combined autoradiographic and immunohistochemical study. , 1985 .

[32]  L. Eng,et al.  Immunocytochemical staining for glial fibrillary acidic protein and the metabolism of cytoskeletal proteins in experimental allergic encephalomyelitis , 1983, Brain Research.

[33]  A. Aguayo,et al.  Extensive elongation of axons from rat brain into peripheral nerve grafts , 1982, Nature.

[34]  L. Guth,et al.  Astroglial reaction in the gray matter of lumbar segments after midthoracic transection of the adult rat spinal cord , 1981, Experimental Neurology.

[35]  L. Amaducci,et al.  Glial fibrillary acidic protein in cryogenic lesions of the rat brain , 1981, Neuroscience Letters.