Jiang Yuxin, Shi Jie, Wang Wenping, Piao Haozhe, Yao Huini, Yu Jun, Zhai Zhenzhu, Liu Qian, Li Ningxin, Fu Jiaqing, Shen Yue, Jin Shengbo, Li Mingzhu
Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China.
Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute, Shenyang, Liaoning, China.
Front Pharmacol. 2025 May 30;16:1609791. doi: 10.3389/fphar.2025.1609791. eCollection 2025.
Oxaliplatin, a third-generation platinum-based chemotherapeutic agent, has shown substantial efficacy in cancer treatment. However, its associated side effects, particularly chemotherapy-induced peripheral neuropathic pain (CIPNP), continue to challenge cancer survivors globally. Clinically, it frequently presents as numbness, coldness, and discomfort in the limbs and extremities. Duloxetine is advised for analgesic purposes. Despite its clinical relevance, both the application methods and the underlying mechanisms of oxaliplatin-induced CINP warrant further investigation. Consequently, more precise animal models are needed to explore the mechanisms and progression of this condition. This review consolidates recent advancements in rat and mouse models of oxaliplatin-induced CINP, with the aim of enhancing modeling success rates and developing models that more accurately mirror disease progression. Such models are essential for advancing clinical research and drug development.
奥沙利铂是一种第三代铂类化疗药物,在癌症治疗中已显示出显著疗效。然而,其相关的副作用,尤其是化疗引起的周围神经病理性疼痛(CIPNP),仍然在全球范围内给癌症幸存者带来挑战。在临床上,它常常表现为四肢麻木、发冷和不适。建议使用度洛西汀进行镇痛。尽管其具有临床相关性,但奥沙利铂诱导的CINP的应用方法和潜在机制仍需进一步研究。因此,需要更精确的动物模型来探索这种疾病的机制和进展。本综述总结了奥沙利铂诱导的CINP大鼠和小鼠模型的最新进展,旨在提高建模成功率,并开发更准确反映疾病进展的模型。此类模型对于推进临床研究和药物开发至关重要。