光老化
化学
免疫印迹
磷酸化
药理学
MAPK/ERK通路
生物碱
氧化应激
生物化学
活性氧
氧化磷酸化
细胞培养
人体皮肤
NF-κB
刺猬信号通路
对接(动物)
毒性
抗氧化剂
氧化损伤
染色体易位
信号转导
结构-活动关系
剂量依赖性
酶
药品
激酶
细胞凋亡
角质形成细胞
MTT法
作者
Guangming Tang,Minqi Chen,Yi Zhang,Zhong‐Ji Qian
标识
DOI:10.1080/14786419.2025.2602908
摘要
Ultraviolet B (UVB) radiation contributes to skin photoaging and inflammation. This study investigated the protective effects of two alkaloids from Aspergillus terreus C23-3 against UVB-irradiated human keratinocytes (HaCaT) and H2O2-stimulated fibroblasts (BJ cells). Alkaloids 1 and 2 effectively protected these cells without toxicity at concentrations ranging from 1 to 10 μM, significantly reducing ROS levels and oxidative stress. Molecular docking indicated that alkaloids 1 and 2 can form stable complexes with MMP-1, and inhibit its activity. This finding was verified by Western blot tests, which demonstrated that alkaloids 1 and 2 could effectively inhibit MMP-1 expression in H2O2-stimulated BJ cells. In addition, alkaloids 1 and 2 can inhibit UVB-induced activation of the MAPK pathway, reducing c-Jun and c-Fos phosphorylation and thereby reducing MMP-1 transcription. By blocking these signalling pathways and possibly inhibiting the nuclear translocation of p65, alkaloids 1 and 2 attenuate UVB-induced inflammatory responses, in particular by reducing the pro-inflammatory markers IL-6, IL-1β, COX-2 and iNOS. Consequently, these alkaloids may have therapeutic potential for alleviating skin photoaging and inflammation.
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