Konczak-Islam Izabela, Yoshimoto Makoto, Hou De-Xing, Terahara Norihiko, Yamakawa Osamu
Food Science Australia, CRC for Bioproducts, Riverside Life Science Centre, 11 Julius Avenue, North Ryde, NSW 2113, Australia.
J Agric Food Chem. 2003 Sep 24;51(20):5916-22. doi: 10.1021/jf030066o.
Anthocyanin-rich aqueous extracts from cell suspension cultures of a high anthocyanin-producing sweetpotato PL (purple line) cell line grown under two different media conditions, MM (multiplication medium) and APM (high anthocyanin-producing medium) and from the cell line's donor tissue, field-grown storage root (SR) of sweetpotato, cv. Ayamurasaki, were evaluated for antioxidative (DPPH test), antimutagenic (Salmonella/reversion assay; mutagen, Trp-P-1), and antiproliferative (human promyelocytic leukaemia cells HL-60) activities. Both cell line extracts MM and APM exhibited higher radical scavenging activities (RSA), 3.8- and 1.4-fold, respectively, than the SR extract. The antimutagenic activity of all extracts was found to be dose-dependent. At a dose of 1 mg/plate, the highest activity exhibited APM (73% inhibition of Trp-P-1-induced reverse mutation of Salmonella typhimurium TA98), followed by MM (54% inhibition) and SR (36% inhibition). The MM extract was the strongest inhibitor of the proliferation of human promyelocytic leukemia cells. At a concentration of 1.6 mg/mL medium during 24 h, it suppressed the growth of 47% of HL-60 cells. A significantly lower growth suppression effect displayed APM and SR extracts (21 and 25%, respectively). Total anthocyanin levels and anthocyanin composition in evaluated samples seem to be related to their activities. The MM extract, which exhibited the highest RSA and antiproliferation activities, contained the highest level of anthocyanins. Among them, nonacylated cyanidin 3-sophoroside-5-glucoside dominated. It is speculated that the presence of this anthocyanin contributed toward enhanced activities of MM extract.
对在两种不同培养基条件(MM,增殖培养基;APM,高花青素产生培养基)下培养的高花青素产量甘薯PL(紫色系)细胞系的富含花青素的水提取物,以及该细胞系的供体组织——田间种植的甘薯品种“绫紫”的贮藏根(SR)进行了抗氧化(DPPH测试)、抗诱变(沙门氏菌/回复突变试验;诱变剂,Trp-P-1)和抗增殖(人早幼粒细胞白血病细胞HL-60)活性评估。细胞系提取物MM和APM的自由基清除活性(RSA)分别比SR提取物高3.8倍和1.4倍。发现所有提取物的抗诱变活性均呈剂量依赖性。在1mg/平板的剂量下,APM表现出最高活性(对Trp-P-1诱导的鼠伤寒沙门氏菌TA98回复突变的抑制率为73%),其次是MM(54%抑制率)和SR(36%抑制率)。MM提取物是人类早幼粒细胞白血病细胞增殖的最强抑制剂。在24小时内,当培养基中浓度为1.6mg/mL时,它抑制了47%的HL-60细胞生长。APM和SR提取物的生长抑制作用明显较低(分别为21%和25%)。评估样品中的总花青素水平和花青素组成似乎与其活性相关。表现出最高RSA和抗增殖活性的MM提取物含有最高水平的花青素。其中,非酰化矢车菊素3-槐糖苷-5-葡萄糖苷占主导。据推测,这种花青素的存在有助于增强MM提取物的活性。