Liu Weixi, Wei Zhengxi, Ma Hang, Cai Ang, Liu Yongqiang, Sun Jiadong, DaSilva Nicholas A, Johnson Shelby L, Kirschenbaum Louis J, Cho Bongsup P, Dain Joel A, Rowley David C, Shaikh Zahir A, Seeram Navindra P
Bioactive Botanical Research Laboratory, Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, RI 02881, USA.
Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, RI 02881, USA.
Food Funct. 2017 Feb 22;8(2):757-766. doi: 10.1039/c6fo01360k.
Oxidative stress and free radical generation accelerate the formation of advanced glycation endproducts (AGEs) which are linked to several chronic diseases. Published data suggest that phenolic-rich plant foods, show promise as natural anti-AGEs agents due to their anti-oxidation capacities. A phenolic-enriched maple syrup extract (MSX) has previously been reported to show anti-inflammatory and neuroprotective effects but its anti-AGE effects remain unknown. Therefore, herein, we investigated the anti-glycation and anti-oxidation effects of MSX using biochemical and biophysical methods. MSX (500 μg mL) reduced the formation of AGEs by 40% in the bovine serum albumin (BSA)-fructose assay and by 30% in the BSA-methylglyoxal (MGO) assay. MSX also inhibited the formation of crosslinks typically seen in the late stage of glycation. Circular dichroism and differential scanning calorimeter analyses demonstrated that MSX maintained the structure of BSA during glycation. In the anti-oxidant assays, MSX (61.7 μg mL) scavenged 50% of free radicals (DPPH assay) and reduced free radical generation by 20% during the glycation process (electron paramagnetic resonance time scan). In addition, the intracellular levels of hydrogen peroxide induced reactive oxygen species were reduced by 27-58% with MSX (50-200 μg mL) in normal/non-tumorigenic human colon CCD-18Co cells. Moreover, in AGEs and MGO challenged CCD-18Co cells, higher cellular viabilities and rapid extracellular signal-regulated kinase (ERK) phosphorylation were observed in MSX treated cells, indicating its protective effects against AGEs-induced cytotoxicity. Overall, this study supports the biological effects of MSX, and warrants further investigation of its potential as a dietary agent against diseases mediated by oxidative stress and inflammation.
氧化应激和自由基生成会加速晚期糖基化终产物(AGEs)的形成,而这些产物与多种慢性疾病有关。已发表的数据表明,富含酚类的植物性食物因其抗氧化能力而有望成为天然抗AGEs剂。此前有报道称,富含酚类的枫糖浆提取物(MSX)具有抗炎和神经保护作用,但其抗AGEs作用尚不清楚。因此,在本文中,我们使用生化和生物物理方法研究了MSX的抗糖基化和抗氧化作用。在牛血清白蛋白(BSA)-果糖试验中,MSX(500μg/mL)使AGEs的形成减少了40%,在BSA-甲基乙二醛(MGO)试验中减少了30%。MSX还抑制了糖基化后期常见的交联形成。圆二色性和差示扫描量热仪分析表明,MSX在糖基化过程中维持了BSA的结构。在抗氧化试验中,MSX(61.7μg/mL)清除了50%的自由基(DPPH试验),并在糖基化过程中使自由基生成减少了20%(电子顺磁共振时间扫描)。此外,在正常/非致瘤性人结肠CCD-18Co细胞中,MSX(50-200μg/mL)使过氧化氢诱导的活性氧细胞内水平降低了27-58%。此外,在AGEs和MGO刺激的CCD-18Co细胞中,在MSX处理的细胞中观察到更高的细胞活力和快速的细胞外信号调节激酶(ERK)磷酸化,表明其对AGEs诱导的细胞毒性具有保护作用。总体而言,本研究支持了MSX的生物学效应,并值得进一步研究其作为抗氧化应激和炎症介导疾病的膳食剂的潜力。