Miyauchi Yu, Soga Shinki, Nanri Hayato, Yonamine Shiori, Ogiwara Takayuki, Kiyama Miho, Kon Risako, Ikarashi Nobutomo, Chiba Yoshihiko, Hosoe Tomoo, Sakai Hiroyasu
Department of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Laboratory of Molecular Biology and Physiology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Calcif Tissue Int. 2025 Jul 9;116(1):96. doi: 10.1007/s00223-025-01406-5.
The systemic administration of cisplatin has been shown to substantially reduce skeletal muscle mass. This is a serious concern, as muscle loss is correlated with increased mortality in patients with cancer. Cisplatin also contributes to cognitive decline, but the exact mechanism thereof remains unclear. In this study, we focused on fibronectin type III domain-containing 5 (Fndc5), a gene that produces irisin, a myokine that is important for brain health. Male C57BL/6J mice (8-9 weeks old) were injected with cisplatin or saline for 4 consecutive days. Twenty-four h after final injection of cisplatin, quadriceps muscles were isolated. C2C12 myotubes were treated with cisplatin with/without AICAR. In male C57BL/6J mice treated with cisplatin, a reduced expression of the key regulator PGC-1α was observed, along with reduced levels of Fndc5/irisin mRNA and protein in the mice quadriceps muscles. Similar findings were seen in cisplatin-treated C2C12 myotube cells, where the activation of PGC-1α with AICAR partially offset these effects. These results suggest that cisplatin inhibits the synthesis of Fndc5/irisin and may contribute to the metabolic changes and cognitive decline observed in patients with cancer who receive this treatment.
顺铂的全身给药已被证明会显著减少骨骼肌质量。这是一个严重问题,因为肌肉流失与癌症患者死亡率增加相关。顺铂还会导致认知能力下降,但其确切机制尚不清楚。在本研究中,我们聚焦于含III型纤连蛋白结构域5(Fndc5),该基因产生鸢尾素,一种对脑健康很重要的肌动蛋白。将雄性C57BL/6J小鼠(8 - 9周龄)连续4天注射顺铂或生理盐水。在最后一次注射顺铂24小时后,分离股四头肌。C2C12肌管在有/无AICAR的情况下用顺铂处理。在用顺铂处理的雄性C57BL/6J小鼠中,观察到关键调节因子PGC - 1α的表达降低,同时小鼠股四头肌中Fndc5/鸢尾素mRNA和蛋白水平也降低。在用顺铂处理的C2C12肌管细胞中也观察到类似结果,其中用AICAR激活PGC - 1α可部分抵消这些影响。这些结果表明,顺铂抑制Fndc5/鸢尾素的合成,可能导致接受该治疗的癌症患者出现代谢变化和认知能力下降。