Jacobs Alison N, Bolstad Luke J, Martinson Natalie, Mickelson Ethan, Ceelen Matthew R, Lefebvre Owen R, Klein Roy Ram, Hellenbrand Daniel J, Hanna Amgad S
Department of Neurological Surgery, University of Wisconsin School of Medicine and Public Health (UWSMPH), Madison, Wisconsin, United States.
Department of Biomedical Engineering, University of Wisconsin Madison, Madison, Wisconsin, United States.
J Brachial Plex Peripher Nerve Inj. 2025 May 29;20(1):e31-e40. doi: 10.1055/a-2591-2757. eCollection 2025 Jan.
Brachial plexus injury (BPI) occurs when the brachial plexus (BP) is compressed, stretched, or avulsed. A mild BPI results in acute arm pain, tingling, or numbness, while more severe injuries can lead to permanent muscle weakness or loss of function of the extremity if left untreated. Many BPI treatments developed in small animal models fail to translate effectively to human clinical trials. Furthermore, there is a lack of comparative studies exploring the anatomical differences between BPs in different species. The objective of this study is to compare the BP anatomy between humans and Sprague-Dawley (SD) rats to determine if the SD rat is a suitable model for studying BPI mechanisms and treatments. Four human BPs were compared to five SD rat BPs. Gross anatomical analysis revealed mild similarities in the branching patterns of SD rat and human BP. Histological results indicated that SD rats had significantly smaller musculocutaneous ( = 0.0095), median ( < 0.0001), and ulnar ( < 0.0001) nerves compared to humans. Additionally, SD rats had significantly fewer axons than humans in the musculocutaneous ( = 0.0190), median ( < 0.0001), and ulnar nerves ( < 0.0001). Due to the anatomical and histological differences between the two species, therapeutic interventions for BPIs developed in rats should be further tested in a larger animal model, such as the Wisconsin Miniature Swine, before progressing to human clinical trials.
臂丛神经损伤(BPI)发生于臂丛神经(BP)受到压迫、牵拉或撕脱时。轻度BPI会导致手臂急性疼痛、刺痛或麻木,而更严重的损伤若不治疗可能会导致永久性肌肉无力或肢体功能丧失。许多在小动物模型中开发的BPI治疗方法未能有效转化为人体临床试验。此外,缺乏探索不同物种臂丛神经解剖学差异的比较研究。本研究的目的是比较人类和Sprague-Dawley(SD)大鼠的臂丛神经解剖结构,以确定SD大鼠是否是研究BPI机制和治疗方法的合适模型。将4例人类臂丛神经与5例SD大鼠臂丛神经进行比较。大体解剖分析显示SD大鼠和人类臂丛神经的分支模式有轻微相似性。组织学结果表明,与人类相比,SD大鼠的肌皮神经(P = 0.0095)、正中神经(P < 0.0001)和尺神经(P < 0.0001)明显更细。此外,SD大鼠肌皮神经(P = 0.0190)、正中神经(P < 0.0001)和尺神经中的轴突数量明显少于人类(P < 0.0001)。由于这两个物种在解剖学和组织学上存在差异,在大鼠中开发的BPI治疗干预措施在进入人体临床试验之前,应在更大的动物模型(如威斯康星小型猪)中进一步测试。