Liu Shu-Ying, Huang Chih-Hao, Shieh Jia-Ching, Lee Tai-Lin
Department of Molecular Biotechnology, Da-Yeh University, Changhua, Taiwan.
J Biosci. 2017 Sep;42(3):439-448. doi: 10.1007/s12038-017-9697-2.
Diabetes patients associated with liver disease carry a significant risk of morbidity and mortality. Cinnamon has been reported to reduce fructose-induced oxidative stress in the rat liver. However, the mechanism by which cinnamon protects the liver in a high-saccharide environment remains to be investigated. HepG2 cells were cultured with 30 mM D-ribose to mimic the high-oxidative-stress environment, typical of a liver in a diabetic patient. Three different chemical types of C. osmophloeum ethanol extracts (CEEs) were added in HepG2 culture media and the administration of all three CEEs protected HepG2 cells from D-ribose damage and increased cell survival by approximately 20 percent. Exclusively, the transcript variant 1 of the ghrelin gene, but not variant 3, was 2-3 times induced by the addition of these CEEs. Moreover, the mRNAs of ghrelin processing enzyme, furin, and mboat4 were detected in HepG2 cells. The ghrelin hormones in the culture media were increased 4-9 times by the addition of CEEs. The protective effects of ghrelin on HepG2 cells in D-ribose environment were further confirmed by recombinant ghrelin transfection. We conclude that the CEEs induce ghrelin gene expression and protect HepG2 cells from D-ribose-induced oxidative damage through ghrelin signalling.
患有肝脏疾病的糖尿病患者面临着较高的发病和死亡风险。据报道,肉桂可降低大鼠肝脏中果糖诱导的氧化应激。然而,肉桂在高糖环境中保护肝脏的机制仍有待研究。用30 mM D-核糖培养HepG2细胞,以模拟糖尿病患者肝脏典型的高氧化应激环境。将三种不同化学类型的肉桂乙醇提取物(CEEs)添加到HepG2培养基中,所有三种CEEs的给药均保护HepG2细胞免受D-核糖损伤,并使细胞存活率提高了约20%。单独地,胃饥饿素基因的转录变体1而非变体3,在添加这些CEEs后被诱导了2至3倍。此外,在HepG2细胞中检测到了胃饥饿素加工酶、弗林蛋白酶和mboat4的mRNA。添加CEEs后,培养基中的胃饥饿素激素增加了4至9倍。重组胃饥饿素转染进一步证实了胃饥饿素在D-核糖环境中对HepG2细胞的保护作用。我们得出结论,CEEs通过胃饥饿素信号传导诱导胃饥饿素基因表达,并保护HepG2细胞免受D-核糖诱导的氧化损伤。