Seo Ji Yeon, Ju Sung Hee, Oh Jisun, Lee Seung Kwon, Kim Jong-Sang
School of Food Science and Biotechnology (BK21 plus), Kyungpook National University , Daegu 41566, Republic of Korea.
Ginseng Research Team, Overseas Business Division, Ilhwa Company, Ltd. , Guri, Gyeonggi-do 11933, Republic of Korea.
J Agric Food Chem. 2016 Apr 13;64(14):2855-64. doi: 10.1021/acs.jafc.5b05789. Epub 2016 Apr 1.
The present study was aimed at elucidating the effect of compound K derived from red ginseng on memory function in mouse model and glutamate-induced cytotoxicity in mouse hippocampal HT22 cells. Compound K induced antioxidant enzymes in nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-mediated manner, and effectively attenuated cytotoxicity and mitochondrial damage induced by glutamate in HT22 cells. However, the cytoprotective effect by compound K was abolished by heme oxygenase-1 inhibitor, tin protophorphyrin IX, suggesting that neuroprotective effect of compound K was caused by its Nrf2-mediated induction of antioxidant enzymes. Further, memory deficit induced by scopolamine was restored by compound K, which did not inhibit acetylcholine esterase, in C57BL/6 mice but not in Nrf2 knockout mice as assessed by passive avoidance test, Y-maze and water maze tests, suggesting that scopolamine-induced memory impairment was overcome by the induction of Nrf2-mediated antioxidant enzymes by the compound K. Overall, our data indicate that compound K could be useful in prevention and treatment of reactive oxygen species-induced neurological disorders such as Alzheimer's disease.
本研究旨在阐明红参衍生的化合物K对小鼠模型记忆功能以及对小鼠海马HT22细胞中谷氨酸诱导的细胞毒性的影响。化合物K以核因子(红细胞衍生2)样2(Nrf2)介导的方式诱导抗氧化酶,并有效减轻HT22细胞中谷氨酸诱导的细胞毒性和线粒体损伤。然而,血红素加氧酶-1抑制剂锡原卟啉IX消除了化合物K的细胞保护作用,这表明化合物K的神经保护作用是由其Nrf2介导的抗氧化酶诱导引起的。此外,通过被动回避试验、Y迷宫和水迷宫试验评估,化合物K可恢复东莨菪碱诱导的C57BL/6小鼠的记忆缺陷,且该化合物不抑制乙酰胆碱酯酶,但对Nrf2基因敲除小鼠无效,这表明化合物K通过诱导Nrf2介导的抗氧化酶克服了东莨菪碱诱导的记忆损伤。总体而言,我们的数据表明化合物K可用于预防和治疗活性氧诱导的神经疾病,如阿尔茨海默病。