Effects of local and systemic treatment with human... - BV FAPESP
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Effects of local and systemic treatment with human natural killer-1 mimetic peptide (HNK-1) after ventral root avulsion and reimplantation in mice

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Autor(es):
Natalia Scanavachia da Silva [1] ; Julia Lombardi [2] ; Frank Kirchhoff ; Rui Seabra Ferreira Jr. [4] ; Benedito Barraviera [5] ; Alexandre Leite Rodrigues de Oliveira [6] ; Luciana Politti Cartarozzi [7]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] University of Campinas. Institute of Biology. Department of Structural and Functional Biology - Brasil
[2] University of Campinas. Institute of Biology. Department of Structural and Functional Biology - Brasil
[4] São Paulo State University. Center for the Study of Venoms and Venomous Animals - Brasil
[5] São Paulo State University. Center for the Study of Venoms and Venomous Animals - Brasil
[6] University of Campinas. Institute of Biology. Department of Structural and Functional Biology - Brasil
[7] University of Campinas. Institute of Biology. Department of Structural and Functional Biology - Brasil
Número total de Afiliações: 7
Tipo de documento: Artigo Científico
Fonte: Journal of Venomous Animals and Toxins including Tropical Diseases; v. 30, 2024-05-20.
Resumo

Abstract Background: Spinal ventral root injuries generate significant motoneuron degeneration, which hinders full functional recovery. The poor prognosis of functional recovery can be attributed to the use or combination of different therapeutic approaches. Several molecules have been screened as potential treatments in combination with surgical reimplantation of the avulsed roots, the gold standard approach for such injuries. Among the studied molecules, human natural killer-1 (HNK-1) stands out as it is related to the stimulation of motor axon outgrowth. Therefore, we aimed to comparatively investigate the effects of local administration of an HNK-1 mimetic peptide (mp-HNK-1) and systemic treatment with ursolic acid (UA), another HNK-1 mimetic, after ventral root avulsion and reimplantation with heterologous fibrin biopolymer (HFB). Methods: Female mice of the isogenic strain C57BL/6JUnib were divided into five experimental groups: Avulsion, Reimplantation, mp-HNK-1 (in situ), and UA (systemic treatment). Mice were evaluated 2 and 12 weeks after surgery. Functional assessment was performed every four days using the Catwalk platform. Neuronal survival was analyzed by cytochemistry, and glial reactions and synaptic coverage were evaluated by immunofluorescence. Results: Treatment with UA elicited long-term neuroprotection, accompanied by a decrease in microglial reactions, and reactive astrogliosis. The neuroprotective effects of UA were preceded by increased glutamatergic and GABAergic inputs in the ventral spinal cord two weeks after injury. However, a single application of mp-HNK-1 had no significant effects. Functional analysis showed that UA treatment led to an improvement in motor and sensory recovery. Conclusion: Overall, the results indicate that UA is neuroprotective, acting on glial cells and synaptic maintenance, and the combination of these findings led to a better functional recovery. (AU)

Processo FAPESP: 21/11936-3 - Centro de Ciência Translacional e Desenvolvimento de Biofármacos
Beneficiário:Benedito Barraviera
Modalidade de apoio: Auxílio à Pesquisa - Centros de Ciência para o Desenvolvimento
Processo FAPESP: 18/05006-0 - Recuperação sensório-motora após axotomia de raízes medulares: emprego de diferentes abordagens experimentais
Beneficiário:Alexandre Leite Rodrigues de Oliveira
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 22/06609-6 - Sinalização glutamatérgica após trauma raquimedular: papel das células da glia na resposta inflamatória e excitotoxicidade
Beneficiário:Luciana Politti Cartarozzi
Modalidade de apoio: Auxílio à Pesquisa - Projeto Geração
Processo FAPESP: 20/01215-4 - Intensificação da regeneração motora com peptídeo mimético de HNK-1 após avulsão e reimplante de raízes ventrais medulares em camundongos C57Bl/6J
Beneficiário:Natália Scanavachia da Silva
Modalidade de apoio: Bolsas no Brasil - Mestrado