Conductive Hydrogel Restores Electrical Conduction to Promote Neurological Recovery in a Rat Model.

IF 3.5 3区 医学 Q3 CELL & TISSUE ENGINEERING Tissue Engineering Part A Pub Date : 2024-09-01 Epub Date: 2024-05-03 DOI:10.1089/ten.TEA.2023.0372
Yichong Zhang, Alina Yao, Jun Wu, Shuhong Li, Minyao Wang, Zexu Peng, Hsing-Wen Sung, Baoguo Jiang, Ren-Ke Li
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Abstract

Spinal cord injury (SCI), caused by significant physical trauma, as well as other pathological conditions, results in electrical signaling disruption and loss of bodily functional control below the injury site. Conductive biomaterials have been considered a promising approach for treating SCI, owing to their ability to restore electrical connections between intact spinal cord portions across the injury site. In this study, we evaluated the ability of a conductive hydrogel, poly-3-amino-4-methoxybenzoic acid-gelatin (PAMB-G), to restore electrical signaling and improve neuronal regeneration in a rat SCI model generated using the compression clip method. Gelatin or PAMB-G was injected at the SCI site, yielding three groups: Control (saline), Gelatin, and PAMB-G. During the 8-week study, PAMB-G, compared to Control, had significantly lower proinflammatory factor expression, such as for tumor necrosis factor -α (0.388 ± 0.276 for PAMB-G vs. 1.027 ± 0.431 for Control) and monocyte chemoattractant protein (MCP)-1 (0.443 ± 0.201 for PAMB-G vs. 1.662 ± 0.912 for Control). In addition, PAMB-G had lower astrocyte and microglia numbers (35.75 ± 4.349 and 40.75 ± 7.890, respectively) compared to Control (50.75 ± 6.5 and 64.75 ± 10.72) and Gelatin (48.75 ± 4.787 and 71.75 ± 7.411). PAMB-G-treated rats also had significantly greater preservation and regeneration of remaining intact neuronal tissue (0.523 ± 0.059% mean white matter in PAMB-G vs 0.377 ± 0.044% in Control and 0.385 ± 0.051% in Gelatin) caused by reduced apoptosis and increased neuronal growth-associated gene expression. All these processes stemmed from PAMB-G facilitating increased electrical signaling conduction, leading to locomotive functional improvements, in the form of increased Basso-Beattie-Bresnahan scores and steeper angles in the slope test (76.667 ± 5.164 for PAMB-G, vs. 59.167 ± 4.916 for Control and 58.333 ± 4.082 for Gelatin), as well as reduced gastrocnemius muscle atrophy (0.345 ± 0.085 for PAMB-G, vs. 0.244 ± 0.021 for Control and 0.210 ± 0.058 for Gelatin). In conclusion, PAMB-G injection post-SCI resulted in improved electrical signaling conduction, which contributed to lowered inflammation and apoptosis, increased neuronal growth, and greater bodily functional control, suggesting its potential as a viable treatment for SCI.

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导电水凝胶恢复电传导,促进大鼠模型的神经功能恢复
脊髓损伤(SCI)是由重大身体创伤和其他病理情况引起的,会导致损伤部位以下的电信号中断和身体功能控制能力丧失。传导性生物材料能够恢复损伤部位完整脊髓部分之间的电连接,因此被认为是治疗脊髓损伤的一种很有前景的方法。在这项研究中,我们评估了导电水凝胶聚-3-氨基-4-甲氧基苯甲酸-明胶(PAMB-G)在使用压迫夹法制作的大鼠 SCI 模型中恢复电信号和改善神经元再生的能力。在脊髓损伤部位注射明胶或 PAMB-G,分为三组:对照组(生理盐水)、明胶组和 PAMB-G 组。在为期 8 周的研究中,与对照组相比,PAMB-G 组的促炎因子表达明显降低,如肿瘤坏死因子 -α (PAMB-G 组为 0.388 ± 0.276,对照组为 1.027 ± 0.431)和单核细胞趋化蛋白 (MCP)-1 (PAMB-G 组为 0.443 ± 0.201,对照组为 1.662 ± 0.912)。此外,与对照组(50.75 ± 6.5 和 64.75 ± 10.72)和明胶(48.75 ± 4.787 和 71.75 ± 7.411)相比,PAMB-G 的星形胶质细胞和小胶质细胞数量较少(分别为 35.75 ± 4.349 和 40.75 ± 7.890)。经 PAMB-G 处理的大鼠还能显著提高剩余完整神经元组织的保存和再生能力(PAMB-G 的平均白质为 0.523 ± 0.059% ,对照组为 0.377 ± 0.044% ,明胶为 0.385 ± 0.051%),这是由于凋亡减少和神经元生长相关基因表达增加所致。所有这些过程都源于 PAMB-G 促进了更多的电信号传导,从而改善了运动功能,具体表现为巴索-巴蒂-布雷斯纳汉评分增加,斜坡测试中角度变陡(对照组为 76.667 ± 5.164,明胶组为 0.385 ± 0.054)。PAMB-G 注射剂为 667 ± 5.164,对照组为 59.167 ± 4.916,明胶注射剂为 58.333 ± 4.082),同时减少了腓肠肌萎缩(PAMB-G 注射剂为 0.345 ± 0.085,对照组为 0.244 ± 0.021,明胶注射剂为 0.210 ± 0.058)。总之,SCI 后注射 PAMB-G 可改善电信号传导,从而减少炎症和细胞凋亡,促进神经元生长,增强身体功能控制,这表明 PAMB-G 有可能成为治疗 SCI 的一种可行方法。
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来源期刊
Tissue Engineering Part A
Tissue Engineering Part A Chemical Engineering-Bioengineering
CiteScore
9.20
自引率
2.40%
发文量
163
审稿时长
3 months
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues.
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