Ayhan Selim, Bozkurt Gokhan, Akbay Atilla, Hayran Mutlu, Ogawa Hiroshi, Yasui Wataru, Tanaka Masato, Ayhan Ayse
Department of Neurological Surgery, Baskent University School of Medicine, Ankara 06490, Turkey.
Department of Neurological Surgery, Hacettepe University School of Medicine, Ankara 06100, Turkey.
Diagnostics (Basel). 2025 Aug 18;15(16):2067. doi: 10.3390/diagnostics15162067.
: Acute spinal cord trauma management necessitates understanding the primary and secondary injury mechanisms at different timepoints. : To characterize the cell death process by examining the temporal and spatial distributions of necrosis and apoptosis in an experimental spinal cord injury model. : Wistar male rats were divided into trauma (n = 30) and sham (n = 6) groups, and a 50 g/cm weight drop contusion design was used. The rats were sacrificed 1, 6, 24, 48, 72, and 168 h after the injury. Every 0.5 cm spinal cord segment was examined cranially and caudally up to a total of 2.5 cm for neuronal and glial damage via the apoptotic count and DNA damage index via morphology and immunohistochemistry using an anti-ssDNA antibody. The results were mapped to visualize the damage extent, intensity, and distribution. : The central zone underwent hemorrhage and necrosis one hour after the injury. The apoptotic cells and DNA damage index increased with time ( < 0.001), and specific spatial alterations were observed among the segments ( < 0.001). Mapping the apoptotic cells and DNA damage clearly reflected the injury's severity and extent. : The DNA damage and the apoptotic cell count increase over time were well correlated with the morphology and could easily be elucidated using ssDNA immunostaining.
急性脊髓损伤的管理需要了解不同时间点的原发性和继发性损伤机制。
通过在实验性脊髓损伤模型中检查坏死和凋亡的时空分布来表征细胞死亡过程。
将雄性Wistar大鼠分为创伤组(n = 30)和假手术组(n = 6),采用50 g/cm重物坠落撞击设计。在损伤后1、6、24、48、72和168小时处死大鼠。通过凋亡计数以及使用抗单链DNA抗体通过形态学和免疫组织化学检测每0.5 cm脊髓节段的神经元和胶质细胞损伤,颅侧和尾侧总共检查2.5 cm。将结果绘制图谱以可视化损伤程度、强度和分布。
损伤后1小时中央区出现出血和坏死。凋亡细胞和DNA损伤指数随时间增加(P < 0.001),并且在各节段间观察到特定的空间变化(P < 0.001)。绘制凋亡细胞和DNA损伤图谱清楚地反映了损伤的严重程度和范围。
DNA损伤和凋亡细胞计数随时间的增加与形态学密切相关,并且使用单链DNA免疫染色很容易阐明。