Gao Jie, Lv Shengtao, Li Changzhi, Tao Jin, Jia Chengqi, Jiang Min, Hou Yuanyuan, Hou Xiaotao, Deng Jiagang, Bai Gang
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, 38 Tongyan Road, Haihe Education Park, Tianjin, 300353 People's Republic of China.
Guangxi Collaborative Innovation Center of Study on Functional Ingredients of Agricultural Residues, Guangxi Key Laboratory of Efficacy Study on Chinese Materia Medica, Guangxi University of Chinese Medicine, Nanning, 530200 People's Republic of China.
J Food Sci Technol. 2017 Aug;54(9):2645-2652. doi: 10.1007/s13197-017-2692-7. Epub 2017 Jul 12.
Grape seed proanthocyanidin extract (GSPE), a type of functional food, possesses potent antioxidant activity. In this study, GSPE protected human embryonic kidney 293 (HEK 293) cells from HO-induced cell injury and oxidative stress in a dose-dependent manner. The key effective constituents that exerted the most potent antioxidative activity in GSPE were screened by using a modified ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q/TOF MS) integrated 2,2'-azinobis(3-ethylbenzothiazoline)-6-sulfonic acid (ABTS) radical cation antioxidative activity analysis system. Two compounds, which were presumed to be Procyanidin B2 and Procyanidin C2, showed obvious antioxidant activity. HO scavenging effect of Procyanidin B2 in HEK 293 cells was visualized in situ by a molecular imaging technique via a novel -borylbenzyloxycarbonyl-3,7-dihydroxyphenoxazine (NBCD) fluorescent probe to detect levels of HO. In conclusion, the application of UPLC-Q/TOF MS integrated modified ABTS radical cation antioxidative activity analysis system and NBCD fluorescent probe successfully screened out and confirmed the antioxidative components from GSPE.
葡萄籽原花青素提取物(GSPE)是一种功能性食品,具有强大的抗氧化活性。在本研究中,GSPE以剂量依赖的方式保护人胚肾293(HEK 293)细胞免受HO诱导的细胞损伤和氧化应激。通过使用改良的超高效液相色谱四极杆飞行时间质谱(UPLC-Q/TOF MS)结合2,2'-偶氮二(3-乙基苯并噻唑啉)-6-磺酸(ABTS)自由基阳离子抗氧化活性分析系统,筛选出了GSPE中发挥最强抗氧化活性的关键有效成分。两种化合物,推测为原花青素B2和原花青素C2,表现出明显的抗氧化活性。通过一种新型的硼基苄氧基羰基-3,7-二羟基吩恶嗪(NBCD)荧光探针,利用分子成像技术在HEK 293细胞中原位观察了原花青素B2对HO的清除作用,以检测HO的水平。总之,UPLC-Q/TOF MS结合改良的ABTS自由基阳离子抗氧化活性分析系统和NBCD荧光探针的应用成功地从GSPE中筛选并确认了抗氧化成分。