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载有埃坡霉素 B 的去细胞神经同种异体移植物增强了大鼠坐骨神经的再生。

Epothilone B loaded in acellular nerve allograft enhanced sciatic nerve regeneration in rats.

机构信息

Department of Biology Education, Faculty of Education, Tishk International University, Erbil, Kurdistan Region, Iraq.

Department of Biology, College of Science, Salahaddin University-Erbil, Iraq.

出版信息

Fundam Clin Pharmacol. 2024 Apr;38(2):307-319. doi: 10.1111/fcp.12961. Epub 2023 Oct 19.

Abstract

BACKGROUND

Epothilone B (EpoB) is a microtubule-stabilizing agent with neuroprotective properties.

OBJECTIVES

This study examines the regenerative properties of ANA supplemented with EpoB on a sciatic nerve deficit in male Wistar rats.

METHODS

For this purpose, the 10 mm nerve gap was filled with acellular nerve allografts (ANAs) containing EpoB at 0.1, 1, and 10 nM concentrations. The sensorimotor recovery was evaluated up to 16 weeks after the operation. Real-time PCR, histomorphometry analysis, and electrophysiological evaluation were also used to evaluate the process of nerve regeneration.

RESULTS

ANA/EpoB (0.1 nM) significantly improved sensorimotor recovery in rats compared to ANA, ANA/EpoB (1 nM), and ANA/EpoB (10 nM) groups. This led to reduced muscle atrophy, improved sciatic functional index, and thermal paw withdrawal reflex latency, indicating nerve regeneration and target organ reinnervation. The electrophysiological and histomorphometry findings also confirmed the ANA/EpoB regenerative properties (0.1 nM). EpoB only enhanced ANA regenerative properties at 0.1 nM, with no therapeutic effects at higher concentrations.

CONCLUSION

Totally, we concluded that ANA loaded with 0.1 nM EpoB can effectively reconstruct the transected sciatic nerve in rats, likely by enhancing axonal sprouting and extension.

摘要

背景

埃坡霉素 B(EpoB)是一种微管稳定剂,具有神经保护作用。

目的

本研究旨在探讨 ANA 联合 EpoB 对雄性 Wistar 大鼠坐骨神经缺损的再生特性。

方法

为此,将含有 0.1、1 和 10 nM 浓度 EpoB 的去细胞同种异体神经移植物(ANAs)填充到 10 mm 的神经间隙中。术后至 16 周评估感觉运动恢复情况。还使用实时 PCR、组织形态计量学分析和电生理评估来评估神经再生过程。

结果

与 ANA、ANA/EpoB(1 nM)和 ANA/EpoB(10 nM)组相比,ANA/EpoB(0.1 nM)显著改善了大鼠的感觉运动恢复。这导致肌肉萎缩减少,坐骨功能指数改善,热足退缩反射潜伏期缩短,表明神经再生和靶器官再支配。电生理和组织形态计量学结果也证实了 ANA/EpoB 的再生特性(0.1 nM)。EpoB 仅在 0.1 nM 时增强了 ANA 的再生特性,而在较高浓度时没有治疗效果。

结论

总之,我们得出结论,负载 0.1 nM EpoB 的 ANA 可有效重建大鼠横断的坐骨神经,可能通过增强轴突发芽和延伸。

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