Abstract:Traumatic root avulsions of the brachial plexus constitute a devastating lesion resulting in loss of function of the upper limb and carry a large emotional and socioeconomic impact. In this literature survey, the different factors involved in root avulsion are discussed in combination with various surgical techniques for repair of experimental ventral root avulsion. Until now repair of root avulsions did not generate unequivocal proof of recovery of limb function, particularly of the hand. More experimental st… Show more
“…Even with this surgical option, reinnervation of muscle does not significantly restore function unless the regenerated axons establish appropriate contacts in a timely fashion, a severe limitation to clinical efficacy because of the inherently slow rate of axon regeneration. Because graft implantation carries its own risks of spinal cord injury, nerve surgeons who perform this procedure have called for optimizing functional outcomes by using neurobiological strategies to improve regeneration (6,10,46). The findings reported here, that sialidase and chondroitinase ABC each enhance axon regeneration into peripheral nerve grafts implanted into the spinal cord, provide two potential therapeutic targets to improve regeneration.…”
Section: Discussionmentioning
confidence: 85%
“…Avulsion occurs in Ͼ70% of brachial plexus injuries (7), and avulsion injury involving the ventral roots has a poor capacity for functional regeneration because of the physical separation of the axons and their nerve sheathes from their corresponding nerve cell bodies within the CNS (9). The mainstay of treatment is surgical and includes palliative surgery, such as nerve or muscle transfers, and restorative surgery, such as the implantation model used in this study (6,(10)(11)(12)(13). Two types of spinal cord implantation can restore connections between ventral horn neurons and their peripheral targets: reimplantation of the avulsed roots into the spinal cord and implantation of grafts between the spinal cord and distal nerve stumps or muscles.…”
Section: Discussionmentioning
confidence: 99%
“…Reimplantation, however, is not an option if the avulsed nerve roots retract, which commonly occurs during the delay between injury and surgery. Although grafts used in humans have ranged from artificial substrata to freezedried muscles, autologous nerve grafts are the most viable (10). Even with this surgical option, reinnervation of muscle does not significantly restore function unless the regenerated axons establish appropriate contacts in a timely fashion, a severe limitation to clinical efficacy because of the inherently slow rate of axon regeneration.…”
Section: Discussionmentioning
confidence: 99%
“…Regaining any sensorimotor function after avulsion, once thought to be impossible, was first accomplished by palliative nerve transfers to provide biceps function and shoulder stability (10). Recently, implantation of avulsed spinal nerve roots or peripheral nerve grafts into the spinal cord to bridge the CNS to the peripheral nervous system has led to functional reconnection in patients, providing a method for restorative surgical treatments (6,11,12).…”
The adult CNS is an inhibitory environment for axon outgrowth, severely limiting recovery from traumatic injury. This limitation is due, in part, to endogenous axon regeneration inhibitors (ARIs) that accumulate at CNS injury sites. ARIs include myelin-associated glycoprotein, Nogo, oligodendrocyte-myelin glycoprotein, and chondroitin sulfate proteoglycans (CSPGs). Some ARIs bind to specific receptors on the axon growth cone to halt outgrowth. Reversing or blocking the actions of ARIs may promote recovery after CNS injury. We report that treatment with sialidase, an enzyme that cleaves one class of axonal receptors for myelinassociated glycoprotein, enhances spinal axon outgrowth into implanted peripheral nerve grafts in a rat model of brachial plexus avulsion, a traumatic injury in which nerve roots are torn from the spinal cord. Repair using peripheral nerve grafts is a promising restorative surgical treatment in humans, although functional improvement remains limited. To model brachial plexus avulsion in the rat, C8 nerve roots were cut flush to the spinal cord and a peroneal nerve graft was inserted into the lateral spinal cord at the lesion site. Infusion of Clostridium perfringens sialidase to the injury site markedly increased the number of spinal axons that grew into the graft (2.6-fold). Chondroitinase ABC, an enzyme that cleaves a different ARI (CSPGs), also enhanced axon outgrowth in this model. In contrast, phosphatidylinositol-specific phospholipase C, which cleaves oligodendrocyte-myelin glycoprotein and Nogo receptors, was without benefit. Molecular therapies targeting sialoglycoconjugates and CSPGs may aid functional recovery after brachial plexus avulsion or other nervous system injuries and diseases.axon regeneration ͉ brachial plexus injury ͉ chondroitinase ABC ͉ gangliosides ͉ spinal cord injury
“…Even with this surgical option, reinnervation of muscle does not significantly restore function unless the regenerated axons establish appropriate contacts in a timely fashion, a severe limitation to clinical efficacy because of the inherently slow rate of axon regeneration. Because graft implantation carries its own risks of spinal cord injury, nerve surgeons who perform this procedure have called for optimizing functional outcomes by using neurobiological strategies to improve regeneration (6,10,46). The findings reported here, that sialidase and chondroitinase ABC each enhance axon regeneration into peripheral nerve grafts implanted into the spinal cord, provide two potential therapeutic targets to improve regeneration.…”
Section: Discussionmentioning
confidence: 85%
“…Avulsion occurs in Ͼ70% of brachial plexus injuries (7), and avulsion injury involving the ventral roots has a poor capacity for functional regeneration because of the physical separation of the axons and their nerve sheathes from their corresponding nerve cell bodies within the CNS (9). The mainstay of treatment is surgical and includes palliative surgery, such as nerve or muscle transfers, and restorative surgery, such as the implantation model used in this study (6,(10)(11)(12)(13). Two types of spinal cord implantation can restore connections between ventral horn neurons and their peripheral targets: reimplantation of the avulsed roots into the spinal cord and implantation of grafts between the spinal cord and distal nerve stumps or muscles.…”
Section: Discussionmentioning
confidence: 99%
“…Reimplantation, however, is not an option if the avulsed nerve roots retract, which commonly occurs during the delay between injury and surgery. Although grafts used in humans have ranged from artificial substrata to freezedried muscles, autologous nerve grafts are the most viable (10). Even with this surgical option, reinnervation of muscle does not significantly restore function unless the regenerated axons establish appropriate contacts in a timely fashion, a severe limitation to clinical efficacy because of the inherently slow rate of axon regeneration.…”
Section: Discussionmentioning
confidence: 99%
“…Regaining any sensorimotor function after avulsion, once thought to be impossible, was first accomplished by palliative nerve transfers to provide biceps function and shoulder stability (10). Recently, implantation of avulsed spinal nerve roots or peripheral nerve grafts into the spinal cord to bridge the CNS to the peripheral nervous system has led to functional reconnection in patients, providing a method for restorative surgical treatments (6,11,12).…”
The adult CNS is an inhibitory environment for axon outgrowth, severely limiting recovery from traumatic injury. This limitation is due, in part, to endogenous axon regeneration inhibitors (ARIs) that accumulate at CNS injury sites. ARIs include myelin-associated glycoprotein, Nogo, oligodendrocyte-myelin glycoprotein, and chondroitin sulfate proteoglycans (CSPGs). Some ARIs bind to specific receptors on the axon growth cone to halt outgrowth. Reversing or blocking the actions of ARIs may promote recovery after CNS injury. We report that treatment with sialidase, an enzyme that cleaves one class of axonal receptors for myelinassociated glycoprotein, enhances spinal axon outgrowth into implanted peripheral nerve grafts in a rat model of brachial plexus avulsion, a traumatic injury in which nerve roots are torn from the spinal cord. Repair using peripheral nerve grafts is a promising restorative surgical treatment in humans, although functional improvement remains limited. To model brachial plexus avulsion in the rat, C8 nerve roots were cut flush to the spinal cord and a peroneal nerve graft was inserted into the lateral spinal cord at the lesion site. Infusion of Clostridium perfringens sialidase to the injury site markedly increased the number of spinal axons that grew into the graft (2.6-fold). Chondroitinase ABC, an enzyme that cleaves a different ARI (CSPGs), also enhanced axon outgrowth in this model. In contrast, phosphatidylinositol-specific phospholipase C, which cleaves oligodendrocyte-myelin glycoprotein and Nogo receptors, was without benefit. Molecular therapies targeting sialoglycoconjugates and CSPGs may aid functional recovery after brachial plexus avulsion or other nervous system injuries and diseases.axon regeneration ͉ brachial plexus injury ͉ chondroitinase ABC ͉ gangliosides ͉ spinal cord injury
“…Brachial plexus trauma occurs when there is traction of the thoracic limb or severe abduction of the scapula (Griffiths, 1974;Steinberg, 1988). Typically, the nerve roots are more likely to be damaged than the plexus itself due to a lower capacity to stretch (Griffiths, 1974;Holtzer et al, 2002;Dewey, 2003).…”
Brachial plexus trauma is a common clinical entity in small animal practice and prognostic indicators are essential early in the course of the disease. Magnetic stimulation of the radial nerve and consequent recording of the magnetic motor evoked potential (MMEP) was examined in 36 dogs and 17 cats with unilateral brachial plexus trauma.Absence of deep pain perception (DPP), ipsilateral loss of panniculus reflex, partial Horner's syndrome and a poor response to MMEP were related to the clinical outcome in 29 of the dogs and 13 of the cats. For all animals, a significant difference was found in MMEP between the normal and the affected limb. Absence of DPP and unilateral loss of the panniculus reflex were indicative of an unsuccessful outcome in dogs. Additionally, the inability to evoke a MMEP was associated with an unsuccessful outcome in all animals. It was concluded that magnetic stimulation of the radial nerve in dogs and cats with brachial plexus trauma may provide an additional diagnostic and prognostic tool.
The anatomical variations of the brachial plexus in humans have clinical significance for surgeons, radiologists, and anatomists. In a study of 60 brachial plexuses, four trunked brachial plexuses were encountered in three limbs (two female and one male), all of them being post fixed and on left side of cadavers. The third trunk in all these limbs gave rise to two anterior divisions (upper and lower) and one posterior division. In two limbs belonging to the female sex, the upper anterior division joined with the anterior division of the second trunk to form the lateral cord while its lower anterior division joined with the anterior division of the fourth trunk to form the medial cord. In the sole male limb, along with the third trunk, the fourth trunk also divided into upper and lower anterior divisions. Upper anterior divisions of the third and fourth trunks joined to form the medial root of the median nerve while lower anterior divisions joined to form the ulnar nerve. No medial cord was formed as such. Further, it is inferred that in postfixed brachial plexus, there is a tendency to failure on part of T1 and T2 to join C8 which continues as the third trunk while T1 and T2 continue as the fourth trunk. Since it was seen in all postfixed brachial plexuses of the present study, it is emphasized to be given a place in the textbooks of anatomy or to conduct a study on a larger database.
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