Ambrosio Sergio R, Furtado Niege A J C, de Oliveira Dionéia C R, da Costa Fernando B, Martins Carlos H G, de Carvalho Tatiane C, Porto Thiago S, Veneziani Rodrigo C S
Núcleo de Pesquisas em Ciências Exatas e Tecnológicas, Universidade de Franca, Franca, SP, Brazil.
Z Naturforsch C J Biosci. 2008 May-Jun;63(5-6):326-30. doi: 10.1515/znc-2008-5-603.
Two kaurane diterpenes, ent-kaur-16(17)-en-19-oic acid (KA) and 15-beta-isovaleryloxy-ent-kaur-16(17)-en-19-oic acid (KA-Ival), isolated from Aspilia foliacea, and the methyl ester derivative of KA (KA-Me) were evaluated against oral pathogens. KA was the most active compound, with MIC values of 10 microg mL(-1) against the following microorganisms: Streptococcus sobrinus, Streptococcus mutans, Streptococcus mitis, Streptococcus sanguinis, and Lactobacillus casei. However, KA did not show significant activity against Streptococcus salivarius and Enterococcus faecalis, with MIC values equal to 100 and 200 microg mL(-1), respectively. Our results show that KA has potential to be used as a prototype for the discovery of new effective anti-infection agents against microorganisms responsible for caries and periodontal diseases. Moreover, these results allow to conclude that minor structural differences among these diterpenes significantly influence their antimicrobial activity, bringing new perspectives to studies on the structure-activity relationship of this type of metabolites with respect to caries and periodontal diseases.
从多叶阿斯皮利亚中分离得到的两种贝壳杉烷二萜类化合物,对映贝壳杉-16(17)-烯-19-酸(KA)和15-β-异戊酰氧基-对映贝壳杉-16(17)-烯-19-酸(KA-Ival),以及KA的甲酯衍生物(KA-Me),对口腔病原体进行了评估。KA是活性最强的化合物,对以下微生物的最低抑菌浓度(MIC)值为10微克/毫升:远缘链球菌、变形链球菌、缓症链球菌、血链球菌和干酪乳杆菌。然而,KA对唾液链球菌和粪肠球菌未显示出显著活性,其MIC值分别为100和200微克/毫升。我们的结果表明,KA有潜力作为发现针对导致龋齿和牙周疾病的微生物的新型有效抗感染药物的原型。此外,这些结果表明,这些二萜类化合物之间的微小结构差异显著影响其抗菌活性,为这类代谢产物与龋齿和牙周疾病相关的构效关系研究带来了新的视角。