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

IF 1.8 3区 医学 Q4 TOXICOLOGY
Natalia Scanavachia da Silva, Julia Lombardi, Frank Kirchhoff, Rui Seabra Ferreira, Benedito Barraviera, Alexandre Leite Rodrigues de Oliveira, Luciana Politti Cartarozzi
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引用次数: 0

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.

小鼠腹侧牙根撕脱和再植后使用人类自然杀伤-1模拟肽(HNK-1)进行局部和全身治疗的效果。
背景:脊髓腹侧根损伤会导致运动神经元严重退化,从而阻碍功能的完全恢复。功能恢复的不良预后可归因于不同治疗方法的使用或组合。目前已筛选出几种分子作为潜在的治疗方法,与手术再植撕脱的神经根(治疗此类损伤的金标准方法)相结合。在所研究的分子中,人类自然杀伤因子-1(HNK-1)脱颖而出,因为它与刺激运动轴突的生长有关。因此,我们旨在比较研究在腹侧根撕脱并用异源纤维蛋白生物聚合物(HFB)再植后,局部注射 HNK-1 拟态肽(mp-HNK-1)和全身注射熊果酸(UA)(另一种 HNK-1 拟态物质)的效果:将同源品系 C57BL/6JUnib 的雌性小鼠分为五个实验组:方法:将同种异源品系 C57BL/6JUnib 的雌性小鼠分为五个实验组:撕脱组、再植组、mp-HNK-1(原位)组和 UA(全身治疗)组。术后 2 周和 12 周对小鼠进行评估。使用 Catwalk 平台每四天进行一次功能评估。通过细胞化学分析神经元存活情况,通过免疫荧光评估神经胶质反应和突触覆盖情况:结果:UA治疗可产生长期的神经保护作用,伴随着小胶质细胞反应和反应性星形胶质细胞增多的减少。在 UA 的神经保护作用之前,损伤两周后脊髓腹侧的谷氨酸能和 GABA 能输入增加。然而,单次应用 mp-HNK-1 并无明显效果。功能分析显示,UA治疗可改善运动和感觉的恢复:总之,研究结果表明,UA 具有神经保护作用,可作用于神经胶质细胞和突触的维持,这些研究结果的结合可促进功能的恢复。
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来源期刊
CiteScore
4.80
自引率
8.30%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Journal of Venomous Animals and Toxins including Tropical Diseases (JVATiTD) is a non-commercial academic open access publication dedicated to research on all aspects of toxinology, venomous animals and tropical diseases. Its interdisciplinary content includes original scientific articles covering research on toxins derived from animals, plants and microorganisms. Topics of interest include, but are not limited to:systematics and morphology of venomous animals;physiology, biochemistry, pharmacology and immunology of toxins;epidemiology, clinical aspects and treatment of envenoming by different animals, plants and microorganisms;development and evaluation of antivenoms and toxin-derivative products;epidemiology, clinical aspects and treatment of tropical diseases (caused by virus, bacteria, algae, fungi and parasites) including the neglected tropical diseases (NTDs) defined by the World Health Organization.
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