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(Reference retrieved automatically from SciELO through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

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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Author(s):
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]
Total Authors: 7
Affiliation:
[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
Total Affiliations: 7
Document type: Journal article
Source: Journal of Venomous Animals and Toxins including Tropical Diseases; v. 30, 2024-05-20.
Abstract

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)

FAPESP's process: 18/05006-0 - Sensorimotor recovery following spinal root axotomy: use of different experimental approaches
Grantee:Alexandre Leite Rodrigues de Oliveira
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 21/11936-3 - Center for Translational Science and Biopharmaceutical Development
Grantee:Benedito Barraviera
Support Opportunities: Research Grants - Science Centers for Development
FAPESP's process: 22/06609-6 - Glutamatergic signaling after rachimedullary trauma: role of glial cells in the inflammatory response and excitotoxicity
Grantee:Luciana Politti Cartarozzi
Support Opportunities: Generation Project Research Grant
FAPESP's process: 20/01215-4 - Intensification of motor regeneration with HNK-1 mimetic peptide after avulsion and reimplantation of medullary ventral roots in C57BL/6J mice
Grantee:Natália Scanavachia da Silva
Support Opportunities: Scholarships in Brazil - Master