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首页> 外文期刊>Journal of Agricultural and Food Chemistry >Chicoric Acid Induces Apoptosis in 3T3-L1 Preadipocytes through ROS-Mediated PI3K/Akt and MAPK Signaling Pathways
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Chicoric Acid Induces Apoptosis in 3T3-L1 Preadipocytes through ROS-Mediated PI3K/Akt and MAPK Signaling Pathways

机译:甲壳酸通过ROS介导的PI3K / Akt和MAPK信号通路诱导3T3-L1前脂肪细胞凋亡

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Chicoric acid has been reported to possess various bioactivities. However, the antiobesity effects of chicoric acid remain poorly understood. In this study, we investigated the effects of chicoric acid on 3T3-L1 preadipocytes and its molecular mechanisms of apoptosis. Chicoric acid inhibited cell viability and induced apoptosis in 3T3-L1 preadipocytes which was characterized by chromatin condensation and poly ADP-ribose-polymerase (PARP) cleavage. Mitochondrial membrane potential (MMP) loss, Bax/Bcl-2 dysregulation, cytochrome c release, and caspase-3 activation were observed, indicating mitochondria-dependent apoptosis induced by chicoric acid. Furthermore, PI3K/Akt and MAPK (p38 MAPK, JNK, and ERK1/2) signaling pathways were involved in chicoric acid-induced apoptosis. The employment of protein kinase inhibitors LY294002, SB203580, SP600125, and U0126 revealed that PI3K/Akt signaling pathway interplayed with MAPK signaling pathways. Moreover, chicoric acid induced reactive oxygen species (ROS) generation. Pretreatment with the antioxidant N-acetylcysteine (NAC) significantly blocked cell death and changes of Akt and MAPK signalings induced by chicoric acid. In addition, chicoric acid down regulated HO-1 and COX-2 via the PI3K/Akt pathway.
机译:据报道,甲壳酸具有多种生物活性。但是,对鸟嘌呤酸的抗肥胖作用仍然知之甚少。在这项研究中,我们研究了菊苣酸对3T3-L1前脂肪细胞的作用及其凋亡的分子机制。甲壳酸抑制细胞活力并诱导3T3-L1前脂肪细胞凋亡,其特征在于染色质浓缩和聚ADP-核糖聚合酶(PARP)裂解。观察到线粒体膜电位(MMP)丢失,Bax / Bcl-2失调,细胞色素c释放和caspase-3激活,表明衣康酸诱导的线粒体依赖性细胞凋亡。此外,PI3K / Akt和MAPK(p38 MAPK,JNK和ERK1 / 2)信号传导途径参与了癸二酸诱导的细胞凋亡。蛋白激酶抑制剂LY294002,SB203580,SP600125和U0126的使用揭示了PI3K / Akt信号通路与MAPK信号通路相互作用。此外,癸酸诱导了活性氧(ROS)的产生。用抗氧化剂N-乙酰半胱氨酸(NAC)预处理可显着阻止细胞死亡以及由癸二酸诱导的Akt和MAPK信号的变化。此外,癸酸通过PI3K / Akt途径下调HO-1和COX-2。

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