Novel anti-inflammatory compounds from Rubus sieboldii, triterpenoids, are inhibitors of mammalian DNA polymerases

Chikako Murakami , Kiyomi Ishijima , Mitsuru Hirota , Kengo Sakaguchi , Hiromi Yoshida , Yoshiyuki Mizushina
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引用次数: 28

Abstract

Two anti-inflammatory triterpenoids, tormentic acid (TA) and euscaphic acid (EA), were found from the plant Rubus sieboldii. These triterpenoids showed an inhibitory effect against enzymes involved in replication, such as calf DNA polymerase α (pol α) and rat DNA polymerase β (pol β). The IC50 values of TA and EA were 37 and 61 μM for pol α and 46 and 108 μM for pol β, respectively. However, TA and EA did not influence the activities of plant DNA polymerases, DNA primase, human immunodeficiency virus type-1 reverse transcriptase, terminal deoxynucleotidyl transferase, any of the prokaryotic DNA polymerases or DNA and RNA metabolic enzymes tested. TA and EA could prevent the growth of BALL-1 cancer cells, and the LD50 values were 11 and 48 μM, respectively. The cells were halted at G1 phase in the cell cycle. The mode of action of the triterpenoids against anti-inflammatory activity and their relationships to the DNA polymerase inhibitory activity and cell growth inhibition were discussed.

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从三叶草中提取的新型抗炎化合物三萜是哺乳动物DNA聚合酶的抑制剂
从三叶草中分离到两种抗炎三萜,分别为折磨酸(tormenic acid, TA)和琥珀酸(euscapic acid, EA)。这些三萜对犊牛DNA聚合酶α (pol α)和大鼠DNA聚合酶β (pol β)等参与复制的酶均有抑制作用。TA和EA对pol α的IC50分别为37和61 μM,对pol β的IC50分别为46和108 μM。然而,TA和EA不影响植物DNA聚合酶、DNA引物酶、人类免疫缺陷病毒1型逆转录酶、末端脱氧核苷酸转移酶、任何原核DNA聚合酶或DNA和RNA代谢酶的活性。TA和EA均能抑制BALL-1癌细胞的生长,LD50值分别为11 μM和48 μM。细胞停止于细胞周期的G1期。讨论了三萜抗炎活性的作用方式及其与DNA聚合酶抑制活性和细胞生长抑制的关系。
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