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Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm

The restoration of voluntary muscle activity in posttraumatic paraplegia in both animal experiments and other clinical applications requires reproducibility of a technically-demanding microsurgical procedure, limited by physicians’ understanding of Brunelli’s spinal cord grafting paradigm. The insuf...

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Autores principales: von Wild, Tobias, Brunelli, Giorgio A., von Wild, Klaus R.H., Löhnhardt, Marlene, Catoi, Cornel, Catoi, Adriana Florinela, Vester, Johannes C., Strilciuc, Stefan, Trillenberg, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993288/
https://www.ncbi.nlm.nih.gov/pubmed/32025252
http://dx.doi.org/10.25122/jml-2019-0063
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author von Wild, Tobias
Brunelli, Giorgio A.
von Wild, Klaus R.H.
Löhnhardt, Marlene
Catoi, Cornel
Catoi, Adriana Florinela
Vester, Johannes C.
Strilciuc, Stefan
Trillenberg, Peter
author_facet von Wild, Tobias
Brunelli, Giorgio A.
von Wild, Klaus R.H.
Löhnhardt, Marlene
Catoi, Cornel
Catoi, Adriana Florinela
Vester, Johannes C.
Strilciuc, Stefan
Trillenberg, Peter
author_sort von Wild, Tobias
collection PubMed
description The restoration of voluntary muscle activity in posttraumatic paraplegia in both animal experiments and other clinical applications requires reproducibility of a technically-demanding microsurgical procedure, limited by physicians’ understanding of Brunelli’s spinal cord grafting paradigm. The insufficient clinical investigation of the long-term benefits of the CNS-PNS graft application warrants additional inquiry. The objective of this study is to explore the potential benefits of the first replicated, graft-induced neuroregeneration of denervated skeletal muscle regarding long-term clinical outcomes and to investigate the effect of Cerebrolysin on neuromodulation. A randomized study evaluating 30 rats, approved by the National Animal Ethics Advisory Committee was performed. The medication was administered postoperatively. For 14 days, 12 rats received Cerebrolysin (serum), 11 received NaCl 0.9% (shams), and 7 were controls. For microsurgery, the lateral corticospinal tract T10 was grafted to the denervated internal obliquus abdominal muscle. On day 90, intraoperative proof of reinnervation was observed. On day 100, 15 rats were euthanized for fixation, organ removal, and extensive histology-morphology examination, and the Wei-Lachin statistical procedure was employed. After an open revision of 16 rats, 8 were CMAP positive. After intravenous Vecuronium application, two (Cerebrolysin, NaCl) out of two rats showed an incomplete compound muscle action potential (CMAP) loss due to glutamatergic and cholinergic co-transmission, while two others showed a complete loss of amplitude. Cerebrolysin medication initiated larger restored muscle fiber diameters and less scarring. FB+ neurons were not observed in the brain but were observed in the Rexed laminae. Brunelli’s concept was successfully replicated, demonstrating the first graft induced existence of cholinergic and glutamatergic neurotransmission in denervated grafted muscles. Statistics of the histometric count of muscle fibers revealed larger fiber diameters after Cerebrolysin. Brunelli’s CNS-PNS experimental concept is suitable to analyze graft-neuroplasticity focused on the voluntary restoration of denervated skeletal muscles in spinal cord injury. Neuroprotection by Cerebrolysin is demonstrated.
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spelling pubmed-69932882020-02-05 Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm von Wild, Tobias Brunelli, Giorgio A. von Wild, Klaus R.H. Löhnhardt, Marlene Catoi, Cornel Catoi, Adriana Florinela Vester, Johannes C. Strilciuc, Stefan Trillenberg, Peter J Med Life Original Article The restoration of voluntary muscle activity in posttraumatic paraplegia in both animal experiments and other clinical applications requires reproducibility of a technically-demanding microsurgical procedure, limited by physicians’ understanding of Brunelli’s spinal cord grafting paradigm. The insufficient clinical investigation of the long-term benefits of the CNS-PNS graft application warrants additional inquiry. The objective of this study is to explore the potential benefits of the first replicated, graft-induced neuroregeneration of denervated skeletal muscle regarding long-term clinical outcomes and to investigate the effect of Cerebrolysin on neuromodulation. A randomized study evaluating 30 rats, approved by the National Animal Ethics Advisory Committee was performed. The medication was administered postoperatively. For 14 days, 12 rats received Cerebrolysin (serum), 11 received NaCl 0.9% (shams), and 7 were controls. For microsurgery, the lateral corticospinal tract T10 was grafted to the denervated internal obliquus abdominal muscle. On day 90, intraoperative proof of reinnervation was observed. On day 100, 15 rats were euthanized for fixation, organ removal, and extensive histology-morphology examination, and the Wei-Lachin statistical procedure was employed. After an open revision of 16 rats, 8 were CMAP positive. After intravenous Vecuronium application, two (Cerebrolysin, NaCl) out of two rats showed an incomplete compound muscle action potential (CMAP) loss due to glutamatergic and cholinergic co-transmission, while two others showed a complete loss of amplitude. Cerebrolysin medication initiated larger restored muscle fiber diameters and less scarring. FB+ neurons were not observed in the brain but were observed in the Rexed laminae. Brunelli’s concept was successfully replicated, demonstrating the first graft induced existence of cholinergic and glutamatergic neurotransmission in denervated grafted muscles. Statistics of the histometric count of muscle fibers revealed larger fiber diameters after Cerebrolysin. Brunelli’s CNS-PNS experimental concept is suitable to analyze graft-neuroplasticity focused on the voluntary restoration of denervated skeletal muscles in spinal cord injury. Neuroprotection by Cerebrolysin is demonstrated. Carol Davila University Press 2019 /pmc/articles/PMC6993288/ /pubmed/32025252 http://dx.doi.org/10.25122/jml-2019-0063 Text en ©Carol Davila University Press This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Original Article
von Wild, Tobias
Brunelli, Giorgio A.
von Wild, Klaus R.H.
Löhnhardt, Marlene
Catoi, Cornel
Catoi, Adriana Florinela
Vester, Johannes C.
Strilciuc, Stefan
Trillenberg, Peter
Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm
title Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm
title_full Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm
title_fullStr Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm
title_full_unstemmed Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm
title_short Regeneration of Denervated Skeletal Muscles – Brunelli’s CNS-PNS Paradigm
title_sort regeneration of denervated skeletal muscles – brunelli’s cns-pns paradigm
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993288/
https://www.ncbi.nlm.nih.gov/pubmed/32025252
http://dx.doi.org/10.25122/jml-2019-0063
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