首页> 外文期刊>Biological & pharmaceutical bulletin >Stimulative Effects of (22E,24R)-Ergosta-7,22-diene-3β,5α,6β-triol from Fruiting Bodies of Tricholoma auratum, on a Mouse Osteoblastic Cell Line, MC3T3-E1
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Stimulative Effects of (22E,24R)-Ergosta-7,22-diene-3β,5α,6β-triol from Fruiting Bodies of Tricholoma auratum, on a Mouse Osteoblastic Cell Line, MC3T3-E1

机译:极地口蘑子实体的(22E,24R)-Ergosta-7,22-diene-3β,5α,6β-三醇对小鼠成骨细胞系MC3T3-E1的刺激作用

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We screened the differentiation-inducing activities of 39 mushroom extracts from Akita prefecture, Japan, on the mouse osteoblastic cell line, MC3T3-E1. Sixteen phosphate buffered saline (PBS), 8 boiled PBS, 14 ethanol and 12 methanol extracts induced alkaline phosphatase (ALP) activities, an indicator of MC3T3-E1 cell differentiation. The enzyme activities were markedly induced by extracts of Tricholoma auratum, and we isolated the active compound from methanol extracts of this mushroom. Physical data for the isolated active compound were identical to those for (22E,24R)-ergosta-7,22-diene-3β,5α,6β-triol (1). 1 induced ALP activities of MC3T3-E1 cells and promoted cell proliferation. To investigate the relationships between the chemical structure and differentiation-inducing activity of the compound, ALP-inducing activities of MC3T3-E1 cells by 1, ergosterol (2), ergocalciferol (3), cholesta-3β,5α,6β-triol (4), 7-dehydrocholesterol (5) and cholecalciferol (6) were tested. The enzyme activities of MC3T3-E1 cells were increased 3.0-fold by 10 μM 1 and 2.4-fold by 10μM 4. However, 2, 3, 5 and 6 did not induce MC3T3-E1 cell ALP activity at 0.1-10 μM. These results suggested that the OH groups at C-5 and/or C-6 of 1 and 4 played an important role in their differentiation-inducing activities on MC3T3-E1 cells. Furthermore, 1 suppressed induction of MC3T3-E1 cell apoptosis by serum starvation.
机译:我们筛选了日本秋田县的39种蘑菇提取物对小鼠成骨细胞系MC3T3-E1的分化诱导活性。 16种磷酸盐缓冲盐水(PBS),8种煮沸的PBS,14种乙醇和12种甲醇提取物可诱导碱性磷酸酶(ALP)活性,这是MC3T3-E1细胞分化的指标。紫口蘑提取物显着诱导了酶的活性,我们从该蘑菇的甲醇提取物中分离了活性化合物。分离出的活性化合物的物理数据与(22E,24R)-麦角七,22-二烯-3β,5α,6β-三醇(1)相同。 1诱导MC3T3-E1细胞的ALP活性并促进细胞增殖。为了研究化合物的化学结构与分化诱导活性之间的关系,1,麦角固醇(2),麦角钙化醇(3),胆甾醇3β,5α,6β-三醇(4)对MC3T3-E1细胞的ALP诱导活性),测试了7-脱氢胆固醇(5)和胆钙化固醇(6)。 MC3T3-E1细胞的酶活性通过10μM1增加了3.0倍,而10μM4增加了2.4倍。但是,在0.1-10μM时,2、3、5和6不会诱导MC3T3-E1细胞的ALP活性。这些结果表明1和4的C-5和/或C-6的OH基团在它们对MC3T3-E1细胞的分化诱导活性中起重要作用。此外,1通过血清饥饿抑制了MC3T3-E1细胞凋亡的诱导。

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