دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: Effects of local and systemic treatment with human natural killer-1 mimetic peptide (HNK-1) after ventral root avulsion and reimplantation in mice
المؤلفون: Natalia Scanavachia da Silva, Julia Lombardi, Frank Kirchhoff, Rui Seabra Ferreira Jr., Benedito Barraviera, Alexandre Leite Rodrigues de Oliveira, Luciana Politti Cartarozzi
المصدر: Journal of Venomous Animals and Toxins including Tropical Diseases, Vol 30 (2024)
بيانات النشر: SciELO, 2024.
سنة النشر: 2024
المجموعة: LCC:Arctic medicine. Tropical medicine
LCC:Toxicology. Poisons
LCC:Zoology
مصطلحات موضوعية: HNK-1 mimetic peptide, Ursolic acid, Heterologous fibrin biopolymer, Neuroprotection, Immunomodulation, Arctic medicine. Tropical medicine, RC955-962, Toxicology. Poisons, RA1190-1270, Zoology, QL1-991
الوصف: 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.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1678-9199
العلاقة: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992024000100305&lng=en&tlng=enTest; http://www.scielo.br/pdf/jvatitd/v30/1678-9199-jvatitd-30-e20230065.pdfTest; https://doaj.org/toc/1678-9199Test
DOI: 10.1590/1678-9199-jvatitd-2023-0065
الوصول الحر: https://doaj.org/article/c77012f38f8848bc9e08033fbfd20b5dTest
رقم الانضمام: edsdoj.77012f38f8848bc9e08033fbfd20b5d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16789199
DOI:10.1590/1678-9199-jvatitd-2023-0065