Carbon Monoxide Alleviates Post-ischemia–reperfusion Skeletal Muscle Injury and Systemic Inflammation

• Published in: Biological & pharmaceutical bulletin Vol. 47; no. 4; pp. 868 - 871
• Main Authors: Taguchi, Kazuaki, Ogaki, Shigeru, Maeda, Hitoshi, Ishima, Yu, Watanabe, Hiroshi, Otagiri, Masaki, Maruyama, Toru
• Format: Journal Article
• Language: English
• Published: Japan The Pharmaceutical Society of Japan 20.04.2024; Japan Science and Technology Agency
• Subjects: Biological activity; Blood flow; Carbon monoxide; Creatine; Creatine kinase; Erythrocytes; Inflammation; Ischemia; ischemia–reperfusion injury; Limbs; muscle; Musculoskeletal system; red blood cell; Reperfusion; Skeletal muscle; Tumor necrosis factor-TNF; carbon monoxide; ischemia–reperfusion injury; muscle; red blood cell
• ISSN: 0918-6158; 1347-5215
• DOI: 10.1248/bpb.b23-00917

Restoration of blood flow in skeletal muscle after a prolonged period of ischemia induces muscular ischemia–reperfusion injury, leading to local injury/dysfunction in muscles followed by systemic inflammatory responses. However, preventive/curative agents for skeletal muscle ischemia injury are unavailable in clinics to date. Increasing evidence has validated that carbon monoxide (CO) prevents the progression of ischemia–reperfusion injury in various organs owing to its versatile bioactivity. Previously, we developed a bioinspired CO donor, CO-bound red blood cells (CO-RBC), which mimics the dynamics of RBC-associated CO in the body. In the present study, we have tested the therapeutic potential of CO-RBC in muscular injury/dysfunction and secondary systemic inflammation induced by skeletal muscle ischemia–reperfusion. The results indicate that CO-RBC rather than RBC alone suppressed elevation of plasma creatine phosphokinase, a marker of muscular injury, in rats subjected to both hind limbs ischemia–reperfusion. In addition, the results of the treadmill walking test revealed a significantly decreased muscular motor function in RBC-treated rats subjected to both hind limbs ischemia–reperfusion than that in healthy rats, however, CO-RBC treatment facilitated sustained muscular motor functions after hind limbs ischemia–reperfusion. Furthermore, CO-RBC rather than RBC suppressed the production of tumour necrosis factor (TNF)-α and interleukin (IL)-6, which were upregulated by muscular ischemia–reperfusion. Interestingly, CO-RBC treatment induced higher levels of IL-10 compared to saline or RBC treatments. Based on these findings, we suggest that CO-RBC exhibits a suppressive effect against skeletal muscle injury/dysfunction and systemic inflammatory responses after skeletal muscle ischemia–reperfusion.