Takeuchi Hisataka, Sakamoto Akio, Ikeguchi Ryosuke, Ohta Souichi, Noguchi Takashi, Ando Maki, Yoshimoto Koichi, Sakamoto Daichi, Matsuda Shuichi
Department of Orthopaedic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
J Reconstr Microsurg. 2023 Feb;39(2):120-130. doi: 10.1055/s-0042-1750082. Epub 2022 Jul 18.
We newly developed a muscle graft that employs a doxorubicin pretreatment technique. The aims of this study were to reveal the biological and morphological features of the muscle tissue in the second week (Study I), to reveal the regeneration outcomes of functional and kinematic assessments of longer-term follow-up (16 weeks, Study II), and to make assessments of the muscle graft with doxorubicin pretreatment in the critical-sized nerve defect model (20 mm, Study III).
A total of 26 adult rats were used in this study. Doxorubicin treatment was accomplished by immersion in a doxorubicin solution for 10 minutes followed by a rinsing procedure. The rats were divided into three groups: the muscle graft with and without doxorubicin pretreatment (M-graft-w-Dox and M-graft-w/o-Dox) groups and the autologous nerve graft (N-graft) group. Assays of apoptosis, immunofluorescent histochemistry including CD68 (macrophage marker), scanning electron microscopy (SEM), morphometrical studies of the regenerated axons, nerve conduction studies, and kinematic studies were performed.
The M-graft-w-Dox group contained significantly larger numbers of apoptotic cells and CD68-positive cells. SEM revealed the existence of the basal lamina, so called "empty tubes," in the M-graft-w-Dox group. Study II showed contentious maturation of the regenerated axons, especially in the compound muscle action potentials. Study III showed that even at 20 mm, the M-graft-w-Dox group promoted axonal regeneration and functional regeneration.
The M-graft-w-Dox group showed superior regeneration results, and this easy and short-term procedure can expand the muscle graft clinical indication for the treatment of peripheral nerve defects.
我们新开发了一种采用阿霉素预处理技术的肌肉移植物。本研究的目的是揭示第二周肌肉组织的生物学和形态学特征(研究I),揭示长期随访(16周,研究II)功能和运动学评估的再生结果,并在临界尺寸神经缺损模型(20毫米,研究III)中评估经阿霉素预处理的肌肉移植物。
本研究共使用26只成年大鼠。通过将大鼠浸入阿霉素溶液10分钟,然后进行冲洗程序来完成阿霉素处理。大鼠被分为三组:有和没有阿霉素预处理的肌肉移植物(M-移植物-w-Dox和M-移植物-w/o-Dox)组以及自体神经移植物(N-移植物)组。进行了凋亡检测、包括CD68(巨噬细胞标志物)的免疫荧光组织化学、扫描电子显微镜(SEM)、再生轴突的形态计量学研究、神经传导研究和运动学研究。
M-移植物-w-Dox组含有明显更多数量的凋亡细胞和CD68阳性细胞。SEM显示M-移植物-w-Dox组存在基膜,即所谓的“空管”。研究II显示再生轴突存在有争议的成熟,特别是在复合肌肉动作电位方面。研究III表明,即使在20毫米时,M-移植物-w-Dox组也促进了轴突再生和功能再生。
M-移植物-w-Dox组显示出优越的再生结果,这种简单且短期的程序可以扩大肌肉移植物治疗周围神经缺损的临床适应证。