Protective Effects of Apamin on Acetaminophen-Induced Hepatotoxicity in Mice

被引:4
|
作者
Jang, Hyo-Jeong [1 ]
Leem, Jaechan [2 ]
Kim, Gyun Moo [3 ]
机构
[1] Keimyung Univ, Sch Med, Dept Pediat, Daegu 42601, South Korea
[2] Daegu Catholic Univ, Sch Med, Dept Immunol, Daegu 42472, South Korea
[3] Daegu Catholic Univ, Sch Med, Dept Emergency Med, Daegu 42472, South Korea
基金
新加坡国家研究基金会;
关键词
acetaminophen; apamin; hepatotoxicity; INDUCED LIVER-INJURY; NF-KAPPA-B; MOUSE MODEL; INFLAMMATION; ACTIVATION; FIBROSIS; PATHWAY; GROWTH; BEE;
D O I
10.3390/cimb45050279
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acetaminophen (APAP) overdose can cause severe liver damage, but therapeutic options are limited. Apamin is a natural peptide present in bee venom and has antioxidant and anti-inflammatory properties. Accumulating evidence suggests that apamin has favorable actions in rodent models of inflammatory disorders. Here, we examined the effect of apamin on APAP-evoked hepatotoxicity. Intraperitoneal administration of apamin (0.1 mg/kg) alleviated histological abnormalities and reduced serum levels of liver enzymes in mice injected with APAP. Apamin inhibited oxidative stress through an increase in the amount of glutathione and activation of the antioxidant system. Apamin also attenuated apoptosis with inhibition of caspase-3 activation. Moreover, apamin reduced serum and hepatic levels of cytokines in APAP-injected mice. These effects were accompanied by suppression of NF-?B activation. Furthermore, apamin inhibited chemokine expression and inflammatory cell infiltration. Our results suggest that apamin dampens APAP-evoked hepatotoxicity through inhibiting oxidative stress, apoptosis, and inflammation.
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页码:4389 / 4399
页数:11
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