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摘要来源:
药物des devel ther。 2023; 17:535-550。 EPUB 2023 2月20日。PMID: 36845666 Chaoliang Lyu,Shanshan Zhang,DeChun Wang
文章隶属关系:cunxin Zhang
摘要:
方法: heaosein(He)蓝色和免疫荧光染色用于鉴定NPC。使用自制细胞加压装置构建了NPC凋亡模型。使用试剂盒检测到增殖活性,活性氧(ROS)含量和凋亡率。使用蛋白质印迹检测到相关蛋白的表达。使用自制的尾骨应力装置构建大鼠尾骨IDD模型。 HE staining and safranine O-fast green FCF cartilage staining were used to observe the degeneration degree of the intervertebral disk.
RESULTS: ADR inhibits static mechanical pressure-induced apoptosis and ROS accumulation in NPCs and improves cell viability. ADR can promote the expression of Heme oxygenase-1 (HO-1), p-Nrf2, p-p38, p-Erk1/2, p-JNK, and other proteins, and its effects can be blocked by inhibitors of the above proteins.
CONCLUSION: ADR can inhibit IDD通过激活MAPK/NRF2/HO-1信号通路并抑制NPC中的静态机械压力诱导的ROS积累。