Li Chi, Yamamoto Toru, Kanemaru Hiroko, Kishimoto Naotaka, Seo Kenji
Division of Dental Anesthesiology, Faculty of Dentistry & Graduate School of Medical and Dental Sciences, Niigata University, Niigata, JPN.
Division of Oral Management Clinic for Medical Cooperation, Niigata University Medical and Dental Hospital, Niigata, JPN.
Cureus. 2024 Nov 15;16(11):e73784. doi: 10.7759/cureus.73784. eCollection 2024 Nov.
This study aims to explore the role of sphingosine-1-phosphate (S1P) in peripheral nerve regeneration after injury. S1P is a crucial metabolite involved in cell migration, inflammation, and nerve regeneration. In this research, six-week-old male Sprague-Dawley rats (total n=18) underwent transection of the inferior alveolar nerve (IAN) and were divided into three groups: S1PR agonist (FTY720) (n=6), saline control (n=6), and S1P1R antagonist (n=6). Regeneration was assessed using immunostaining and retrograde tracing. Results showed that the S1PR agonist group had superior axonal and Schwann cell regeneration compared to controls. Additionally, the combination with S1P1R antagonists inhibited the effects of the agonists, further confirming the potential role of S1P1R in nerve repair. Our results suggest that mediating S1P1R signaling could facilitate the regeneration of peripheral nerves after injury.
本研究旨在探讨1-磷酸鞘氨醇(S1P)在损伤后周围神经再生中的作用。S1P是一种参与细胞迁移、炎症和神经再生的关键代谢产物。在本研究中,将六周龄雄性Sprague-Dawley大鼠(共18只)的下牙槽神经(IAN)横断,并分为三组:S1PR激动剂(FTY720)组(n = 6)、生理盐水对照组(n = 6)和S1P1R拮抗剂组(n = 6)。使用免疫染色和逆行追踪评估神经再生情况。结果显示,与对照组相比,S1PR激动剂组具有更好的轴突和雪旺细胞再生。此外,S1P1R拮抗剂的联合使用抑制了激动剂的作用,进一步证实了S1P1R在神经修复中的潜在作用。我们的结果表明,介导S1P1R信号传导可促进损伤后周围神经的再生。