首页> 外文期刊>Oncology Research >Pu-erh Tea Supplementation Suppresses Fatty Acid Synthase Expression in the Rat Liver Through Downregulating Akt and JNK Signalings as Demonstrated in Human Hepatoma HepG2 Cells
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Pu-erh Tea Supplementation Suppresses Fatty Acid Synthase Expression in the Rat Liver Through Downregulating Akt and JNK Signalings as Demonstrated in Human Hepatoma HepG2 Cells

机译:普-茶补品通过下调Akt和JNK信号来抑制人肝癌HepG2细胞中显示的脂肪酸合酶在大鼠肝脏中的表达。

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Fatty acid synthase (FAS) is a key enzyme of lipogenesis, Overexpression of FAS is dominant in cancer cells and proliferative tissues. The expression of FAS in the livers of rats fed pu-erh tea leaves was significantly suppressed. The gains in body weight, levels of triacylglycerol, and total cholesterol were also suppressed in the tea-treated rats, FAS expression in hepatoma HepG2 cells was suppressed by the extracts of pu-erh tea at both the protein and mRNA levels, FAS expression in HepG2 cells was strongly inhibited by PBK inhibitor LY294002 and INK inhibitor II and slightly inhibited by p38 inhibitor SB203580 and MEK inhibitor PD98059, separately. Based on these findings, we suggest that the suppression of FAS in the livers of rats fed pu-erh tea leaves may occur through downregulation of the PI3K/AKt and INK signaling pathways The major components of tea that have been demonstrated to be responsible for the antiobesity and hypolipidemic effects are catechins, caffeine, and theanine. The compositions of catechins, caffeine, and theanine varied dramatically in pu-erh, black, oolong, and green teas. The active principles and molecular mechanisms that exerted these biological effects in pu-erh tea deserve future exploration.
机译:脂肪酸合酶(FAS)是脂肪生成的关键酶,FAS的过表达在癌细胞和增生组织中占主导地位。饲喂普-茶的大鼠肝脏中FAS的表达被显着抑制。茶处理的大鼠体重,三酰甘油水平和总胆固醇的增加也被抑制,普oma茶提取物在蛋白和mRNA水平上抑制了肝癌HepG2细胞中FAS的表达,在肝脏中FAS的表达受到抑制。 HepG2细胞分别被PBK抑制剂LY294002和INK抑制剂II强烈抑制,而分别被p38抑制剂SB203580和MEK抑制剂PD98059轻微抑制。根据这些发现,我们认为,通过下调PI3K / AKt和INK信号传导途径,可以抑制普fed茶喂养大鼠肝脏中FAS的表达。肥胖和降血脂作用是儿茶素,咖啡因和茶氨酸。普-茶,红茶,乌龙茶和绿茶中儿茶素,咖啡因和茶氨酸的成分差异很大。在普-茶中发挥这些生物学作用的有效原理和分子机制值得进一步探索。

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