Department of Orthopedic Surgery, Shanghai Jiao Tong University Affiliated No.6 People's Hospital, 600 Yishan Road, Shanghai 200233, China.
Biomed Res Int. 2021 Jul 10;2021:3376496. doi: 10.1155/2021/3376496. eCollection 2021.
Lactobacillus rhamnoides, a human intestinal colonizer, can act through various pathways to induce microglia/macrophages to produce cytokines and to polarize microglia/macrophages to different phenotypes to reduce the inflammatory response. In this article, we evaluated the treatment potential of the Lactobacillus rhamnoides GG conditioned medium (LGG-CM) in rat model with SCI (acute spinal cord injury), including functional, neurophysiological, and histological outcomes and the underlying neuroprotective mechanisms. In our experiment, LGG-CM (30 mg/kg) was injected directly into the injury site in rats immediately after SCI. Measured by the BBB scale (Basso, Beattie, and Bresnahan locomotor rating scale) and inclined plane test, rats in the LGG-CM-treated group showed better locomotor scores. Moreover, compared to the vehicle treatment group, LGG-CM increased the mRNA level of the M2 marker (CD206), and decreased that of the M1 marker (iNOS). Western blot assays showed that LGG-CM-treated SCI rats had a higher grayscale ratio of p65 and a lower ratio of p-IB/IB. Our study shows that local injection of LGG-CM after acute SCI can inhibit inflammatory responses and improve motor function recovery. These effects may be related with the inhibition to the NF-B (The nuclear factor-kappa B) signal pathway which leads to M2 microglia/macrophage polarization.
鼠李糖乳杆菌是一种人类肠道定植菌,可通过多种途径诱导小胶质细胞/巨噬细胞产生细胞因子,并将小胶质细胞/巨噬细胞极化为不同表型,从而减轻炎症反应。在本文中,我们评估了鼠李糖乳杆菌 GG 条件培养基(LGG-CM)在 SCI(急性脊髓损伤)大鼠模型中的治疗潜力,包括功能、神经生理和组织学结果以及潜在的神经保护机制。在我们的实验中,LGG-CM(30mg/kg)在 SCI 后立即直接注射到损伤部位。通过 BBB 量表(Basso、Beattie 和 Bresnahan 运动评分量表)和斜面试验测量,LGG-CM 治疗组的大鼠表现出更好的运动评分。此外,与载体处理组相比,LGG-CM 增加了 M2 标志物(CD206)的 mRNA 水平,并降低了 M1 标志物(iNOS)的水平。Western blot 检测显示,LGG-CM 处理的 SCI 大鼠 p65 的灰度比值较高,p-IB/IB 的比值较低。我们的研究表明,急性 SCI 后局部注射 LGG-CM 可抑制炎症反应并改善运动功能恢复。这些效果可能与 NF-B(核因子-kappa B)信号通路的抑制有关,从而导致 M2 小胶质细胞/巨噬细胞极化。