Cherdshewasart Wichai, Sutjit Wandee, Pulcharoen Kade, Chulasiri Malyn
Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.
Biosci Biotechnol Biochem. 2010;74(5):923-7. doi: 10.1271/bbb.90727. Epub 2010 May 7.
Butea superba is a traditional tuberous Thai plant enriched with flavonoids that is used for treating erectile dysfunction. We investigated the mutagenic and antimutagenic potentials of a B. superba extract by using the pre-incubation method of the Ames test. Salmonella typhimurium strains TA 98 and TA 100 were applied as the tester strains in the presence and absence of an S9 mixture. Prior to the mutagenic and antimutagenic tests, the survival of the tester strains was measured by treating with the B. superba extract. The results show that the B. superba extract exhibited dose-dependent cytotoxic effects. Data from the Ames test revealed that the B. superba extract to be non-mutagenic in the presence and absence of the S9 mixture. In contrast, the B. superba extract showed antimutagenic potential towards either or both of the tested mutagens: 2-(2-furyl)-3-(5-nitro-2-furyl)-acrylamide (AF-2) and benzo(a)pyrene (B(a)P) in the respective presence and absence of the S9 mixture, respectively. The plant antimutagenic activity was confirmed by a rec assay. A further study by micronucleus test demonstrated that the B. superba extract at the maximum loading volume could induce acute micronucleus formation in the tested animals. The in vitro mutagenic and antimutagenic assays confirmed the safe consumption of B. superba products at low dose (not more than 781.25 microg/ml of the plant extract), but the in vivo genotoxic assay demonstrated the unsafe consumption at a high dose (300 mg/kg of the BW plant extract or 16 g/kg of the BW plant powder).
艳紫铆是一种富含类黄酮的泰国传统块茎植物,用于治疗勃起功能障碍。我们采用Ames试验的预孵育法研究了艳紫铆提取物的致突变和抗突变潜力。鼠伤寒沙门氏菌菌株TA 98和TA 100在有和没有S9混合物的情况下用作测试菌株。在进行致突变和抗突变试验之前,通过用艳紫铆提取物处理来测量测试菌株的存活率。结果表明,艳紫铆提取物表现出剂量依赖性细胞毒性作用。Ames试验数据显示,艳紫铆提取物在有和没有S9混合物的情况下均无致突变性。相反,艳紫铆提取物分别在有和没有S9混合物的情况下,对两种测试诱变剂中的一种或两种:2-(2-呋喃基)-3-(5-硝基-2-呋喃基)-丙烯酰胺(AF-2)和苯并(a)芘(B(a)P)表现出抗突变潜力。通过重组试验证实了该植物的抗突变活性。微核试验的进一步研究表明,最大加载量的艳紫铆提取物可在受试动物中诱导急性微核形成。体外致突变和抗突变试验证实了低剂量(植物提取物不超过781.25微克/毫升)的艳紫铆产品的安全食用性,但体内遗传毒性试验表明高剂量(体重300毫克/千克的植物提取物或体重16克/千克的植物粉末)的食用不安全。