Sarmento Ulana Chaves, Miguita Carlos Henrique, Almeida Luís Henrique de Oliveira, Gaban Cleusa Rocha Garcia, Silva Lilliam May Grespan Estodutto da, Souza Albert Schiaveto de, Garcez Walmir Silva, Garcez Fernanda Rodrigues
Universidade Federal de Mato Grosso do Sul, Universidade Federal de Mato Grosso do Sul, Instituto de Química, Campo Grande MS , Brasil, Universidade Federal de Mato Grosso do Sul, Instituto de Química, Campo Grande, MS, Brasil.
Universidade Federal de Mato Grosso do Sul, Universidade Federal de Mato Grosso do Sul, Centro de Ciências Biológicas e da Saúde, Campo Grande MS , Brasil, Universidade Federal de Mato Grosso do Sul, Centro de Ciências Biológicas e da Saúde, Campo Grande, MS, Brasil.
Mem Inst Oswaldo Cruz. 2016 Jun 20;0(7):0. doi: 10.1590/0074-02760160134.
A total of 36 ethanol extracts from different anatomical parts of 27 plant species (18 families), native to the Pantanal and Cerrado biomes in Midwest Brazil, was assessed for their effect against Aedes aegypti larvae, the vector of dengue, hemorrhagic dengue, Zika and chikungunya fevers. Only the extract obtained from seeds of Guarea kunthiana (Meliaceae) proved active (LC50 = 169.93 μg/mL). A bioassay-guided investigation of this extract led to the isolation and identification of melianodiol, a protolimonoid, as the active constituent (LC50 = 14.44 mg/mL). Meliantriol, which was also obtained from the bioactive fraction, was nevertheless devoid of any larval toxicity, even at the highest concentration tested (LC50 > 100.0 mg/mL). These results indicate that the larvicidal activity of melianodiol stems from the presence of the carbonyl moiety at C-3 in the 21,23-epoxy-21,24,25-trihydroxy-tirucall-7-ene-type skeleton. The structures of both protolimonoids were established on the basis of spectral methods (1H and 13C NMR and MS). This is the first report on the toxicity of melianodiol against Ae. aegypti larvae. Based on the results, melianodiol can be regarded as a potential candidate for use as an ecologically sound biocontrol agent for reducing the larval population of this vector.
对来自巴西中西部潘塔纳尔湿地和塞拉多生物群落的27种植物(18个科)不同解剖部位的36种乙醇提取物进行了评估,以研究其对埃及伊蚊幼虫(登革热、出血性登革热、寨卡病毒和基孔肯雅热的传播媒介)的作用。结果发现,只有昆氏割舌树(楝科)种子提取物具有活性(LC50 = 169.93 μg/mL)。对该提取物进行生物测定导向的研究后,分离并鉴定出一种原柠檬苦素类化合物——苦楝二醇为活性成分(LC50 = 14.44 mg/mL)。从生物活性部分中还得到了苦楝三醇,但即便在测试的最高浓度下,它也没有任何幼虫毒性(LC50 > 100.0 mg/mL)。这些结果表明,苦楝二醇的杀幼虫活性源于其在21,23-环氧-21,24,25-三羟基-四环三萜-7-烯型骨架的C-3位上存在羰基部分。两种原柠檬苦素类化合物的结构均通过光谱方法(1H和13C NMR以及MS)确定。这是关于苦楝二醇对埃及伊蚊幼虫毒性的首次报道。基于这些结果,苦楝二醇可被视为一种潜在的候选物,用作减少该媒介幼虫数量的生态友好型生物防治剂。