芹菜素
超氧化物歧化酶
氧化应激
药理学
血尿素氮
肌酐
肾
谷胱甘肽过氧化物酶
化学
p38丝裂原活化蛋白激酶
抗氧化剂
医学
内科学
生物化学
MAPK/ERK通路
激酶
类黄酮
作者
Xuexiu He,Chunmei Li,Zhengkai Wei,Jingjing Wang,Jinhua Kou,Weijian Liu,Mingyu Shi,Zhengtao Yang,Yunhe Fu
标识
DOI:10.1016/j.ejphar.2016.07.003
摘要
This study aimed to investigate the effects and molecular mechanisms of the effects of apigenin on cisplatin (CP)-induced kidney injury in mice. Apigenin was intraperitoneally administered for 3 consecutive days before CP treatment. We found that apigenin pretreatment significantly attenuated the damage to the kidneys and decreased the levels of serum creatinine, blood urea nitrogen (BUN), glutathione peroxidase (GSH-PX) and superoxide dismutase (SOD), which were increased by CP. Apigenin significantly decreased the levels of TNF-α, IL-1β and TGFβ in the kidneys. Additionally, apigenin inhibited the activations of CYP2E1, phospho-NF-κB p65 and phospho-P38 MAPK in CP-induced renal injury. These results suggest that the renoprotective effects of apigenin may be related to the suppressions of oxidative stress and inflammation in CP-induced renal injury in mice.
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