PI3K/AKT/mTOR通路
药理学
蛋白激酶B
神经化学
神经病理性疼痛
敏化
医学
伤害
化学
信号转导
神经学
受体
内科学
免疫学
生物化学
精神科
作者
Dandan Zhang,Qiaoqiao Chen,Li Yao
标识
DOI:10.1007/s12640-022-00531-5
摘要
Neuropathic pain (NP) is a common disorder among individuals worldwide, but there is still no effective treatment for NP. The EGFR pathway promotes NP nociceptive sensitization and represents a potential therapeutic target. Geniposide is abundant in natural plants and has various pharmacological activities, such as analgesia and anti-inflammation properties, which can improve NP, but the specific mechanisms have not been elucidated. The present study first predicted and molecularly docked geniposide targets, suggesting that geniposide may play a role in improving NP by targeting EGFR. This study further clarified that geniposide alleviates NP and improves the inflammatory response using a chronic constriction injury (CCI) model, whereas the administration of an EGFR agonist weakens the above effects of geniposide. Analysis of transcriptome data further suggests that geniposide not only improves CCI symptoms by reducing EGFR/PI3K/AKT pathway activity but also may exert anti-inflammatory effects by inhibiting the Ca2+ signaling pathway. The above results affirm the potential value of geniposide in the treatment of NP and lay the foundation for further clinical application.
科研通智能强力驱动
Strongly Powered by AbleSci AI