In vitro growth inhibition and bactericidal activity of spathulenol against drug-resistant clinical isolates of Mycobacterium tuberculosis

ABSTRACT Spathulenol was isolated from an extract of Azorella compacta Phil., Apiaceae, by various chromatographic method; identification of the chemical structure was confirmed by comparing its spectroscopic data with those reported in the literature. The anti-Mycobacterium tuberculosis activity of spathulenol was evaluated on MDR, pre-XDR, and XDR clinical isolates of M. tuberculosis, as well as on the reference susceptible strain H37Rv and its cytotoxic activity was evaluated on the Vero Cell Line. The anti-M. tuberculosis activity of spathulenol was twice as potent against the MDR, pre-XDR, and XDR clinical isolates (6.25 µg/ml) than on the susceptible H37Rv strain (12.5 µg/ml). Additionally, the anti-M. tuberculosis activity shown by spathulenol was established as bactericidal on drug-resistant and susceptible strains of M. tuberculosis. Finally, cytotoxic activity on the Vero cell line (CC50 = 95.7 µg/ml) indicated that spathulenol is a selective anti-M. tuberculosis compound, with a selective index of 15.31 against drug-resistant clinical isolates of M. tuberculosis.

Biocidal potential of Eugenia pyriformis essential oil in the control of Rhipicephalus (Boophilus) microplus in the free-living cycle / Potencial biocida do óleo essencial de Eugenia pyriformis Cambess no controle de Rhipicephalus (Boophilus) microplus no ciclo de vida livre

Brazil has one of the largest commercial cattle herds in the world, which naturally coexist with an enormous number of parasitic species. Southern cattle tick, Rhipicephalus (Boophilus) microplus, is among these species, interfering with animal productivity and causing losses to the beef and dairy cattle sector. The use of chemical acaricides in the control of this mite has resulted in the emergence of resistant populations. In this sense, alternative control measures using plants as sources of botanical acaricides have shown to be effective. Eugenia pyriformis Cambess is a Brazilian plant with antioxidant and antimicrobial activity; however, there are no reports on its acaricidal activity in the literature. The present study aimed to evaluate the acaricidal and larvicidal potential of E. pyriformis leaf essential oil (EO) on southern cattle tick at different stages of the reproductive cycle. E. pyriformis leaves were collected and dried, and had their EO extracted by hydrodistillation (3h) using a modified Clevenger apparatus. Chemical analysis was performed by gas chromatography coupled with mass spectrometry (GC/MS), and 32 compounds belonging to the sesquiterpene class were identified: hydrocarbons (17.98%) and oxygenated forms (81.96%), with spathulenol (43.65%) and caryophyllene oxide (12.17%) as the most common. The EO was evaluated by the Adult Immersion Test at the concentrations (500.00 to 3.12mg/mL) in which the following parameters were measured: mortality of females (%), hatchability of eggs (%), and product efficiency (%). Larvae were assessed by the Larval Packet Test at concentrations ranging from 25.00 to 0.00004mg/mL. Lethal concentrations (LC) required for killing 50 and 99.9% of adult females and larvae were determined using Probit analysis. LC50 and LC99.9 of EO were 0.06 and 24.60mg/mL and 1,208.80 and 2,538mg/mL for larvae and adult females, respectively. Action of the EO in the free-living cycle of R. (B.) microplus larvae was another parameter assessed. To this end, the larvae were deposited in pots containing Brachiaria decumbens and, after migration to the leaf apex, a solution containing LC99.9 (24.60mg/mL) of the EO was sprayed. After 24h, 72.25% of the larvae had died, indicating stability of the EO when subjected to uncontrolled temperature and humidity conditions. The mechanism of action through which the EO killed the larvae and adult females was investigated by the Bioautographic Method, which showed inhibition of 3.15mg/mL of the EO on the acetylcholinesterase (AChE) enzyme. The results found in the present experiment indicate that E. pyriformis essential oil is an alternative in the control of southern cattle tick in the larval (parasitic) and free-living cycle (non-parasitic) stages under field conditions.(AU)

O Brasil dispõe de um dos maiores rebanhos bovinos comerciais do mundo, sendo natural que junto a esse rebanho, coexista uma enorme quantidade de espécies parasitárias; dentre estes o carrapato Rhipicephalus (Boophilus) microplus que interfere na produtividade animal, causando prejuízos à pecuária de corte e leite. A utilização de acaricidas químicos no controle deste ácaro tem causado o surgimento de populações resistentes e neste sentido, controles alternativos utilizando plantas como fontes de acaricidas botânicos têm se mostrado eficazes. Eugenia pyriformis Cambess é uma planta brasileira com atividades antioxidante e antimicrobiana, entretanto não há relatos da atividade acaricida. O objetivo do presente estudo consistiu na avaliação do potencial acaricida e larvicida do óleo essencial das folhas de E. pyriformis sobre o carrapato bovino nos diferentes estágios do ciclo reprodutivo. As folhas foram coletadas, secas e o OE extraído por hidrodestilação (3 horas) em aparelho Clevenger modificado. A análise química foi realizada por cromatografia gasosa acoplada à espectrometria de massas (CG/EM) sendo identificados 32 compostos, pertencentes à classe sesquiterpenos: hidrocarbonetos (17.98%) e oxigenados (81.96%); tendo como majoritários o spathulenol (43,65%) e caryophylene oxide (12,17%). O OE foi avaliado pelo teste de imersão de adultos nas concentrações (500,00 a 3,12mg/mL) onde foram mensurados os parâmetros: mortalidade das fêmeas (%), eclodibilidade dos ovos (%) e eficiência do produto (%). As larvas foram avaliadas pelo teste de imersão larval (Larval Packet Test) nas concentrações que variaram de 25,00 a 0,00004mg/mL. Foram determinadas as concentrações letais (CLs) necessárias para matar 50 e 99,9% das fêmeas adultas e das larvas utilizando a análise de Probitos. As CL50 e CL99,9 do OE foram (0,06 e 24,60mg/mL) para as larvas e (1.208,80 e 2.538mg/mL) para as fêmeas adultas, respectivamente. Outro parâmetro avaliado em nossa pesquisa foi mensurar a ação do OE no ciclo de vida livre das larvas de R.(B.) microplus; onde as larvas foram depositadas em vasos com Brachiaria decumbens e após migração destas para o ápice das folhas, foi aspergido solução contendo a CL99,9 (24,60mg/mL) do OE. Após 24 horas, 72,25% das larvas morreram indicando que houve estabilidade do OE quando submetido a condições de temperatura e umidade não controladas. O mecanismo de ação pelo qual o OE matou as larvas e fêmeas adultas foi investigado pelo método bioautográfico, indicando uma inibição de 3,15mg/mL do óleo essencial sobre a enzima acetilcolinesterase (AChE). Os resultados encontrados no presente experimento indicaram que o óleo essencial de E. pyriformis é uma alternativa no controle do carrapato bovino no estágio larval (parasitário) e no ciclo de vida livre (estágio não parasitário) em condições de campo.(AU)

Sesquiterpenes from aerial parts of Hyssopus cuspidatus / 中草药

Objective To study the sesquiterpenes from the aerial parts of Hyssopus cuspidatus. Methods The compounds were isolated and purified by a combination of various chromatographic techniques including D101 macroporous adsorption resin, silica gel, ODS, Toyopearl HW-40C, Sephadex LH-20, and semi-preparative HPLC. Their structures were elucidated on the basis of physicochemical properties and spectroscopic data. Results Fifteen sesquiterpenes were isolated from the 95% EtOH extracts of H. cuspidatus and their structures were elucidated as 3-eudesmene-1β-11-diol (1), 4-eudesmene-1β,11-diol (2), 1β,11-dihydroxy-5- eudesmene (3), ent-4(15)-eudesmen-1α,11-diol (4), 7α,11-dihydroxy-cadin-10(14)-ene (5), eudesmane-1β,5α,11-triol (6), 5-epi- eudesma-4(15)-ene-1β,6β-diol (7), 4(15)-eudesmene-1β,6α-diol (8), (7R*)-opposit-4(15)-ene-1β,11-diol (9), cryptomeridiol (10), octahydro-4-hydroxy-3α-methyl-7-methylene-α-(1-methylethyl)-1H-indene-1-methanol (11), caryolane-1,9β-diol (12), (3S,5R,6S,7E)- 3,5,6-trihydroxy-7-megastigmen-9-one (13), spathulenol (14), and 4β,10α-aromadendranediol (15), respectively. Conclusion Compounds 1-15 are isolated from the plants of Hyssopus genus for the first time.

Composition, antioxidant properties, and biological activities of the essential oil extracted from Ocotea diospyrifolia (Meisn.) Mez

The article has aimed to characterize the essential oil extracted from Ocotea diospyrifolia (Meisn.) Mez. leaves, in terms of its chemical composition and antioxidant, hemolytic, and phytotoxic potentials, as well as its toxicity against Artemia salina. The major constituents identified by CG-MS were d-elemene, spathulenol, and b-atlantol. When screened for potential biological activities, the essential oil presented low toxicity against Artemia salina, and a capacity of lysing red blood cells. Also, the evaluation of its in vitro antioxidant activity, using the phosphomolybdenum method, showed better results when compared to butylhydroxytoluene (BHT) and rutin. In conclusion, the results obtained showed certain in vitro toxicity, leading to an interesting target for cytotoxicity evaluations of carcinoma cells.

First phytochemical description of essential oils from Piper cachimboense (Piperales, Piperaceae) / Primeira descrição fitoquímica de óleos essenciais de Piper cachimboense (Piperales, Piperaceae)

Piper cachimboense is recorded only for the Amazon region of Brazil and Colombia, and the objective of this study was to report the first phytochemical assessment of the composition of the essential oils (EOs) from this species collected in the Amazon rainforest, in Novo Progresso, Pará State, Brazil. Samples of leaves were subjected to hydrodistillation in a Clevenger-type apparatus. The chemical identification was carried out by gas chromatography. The yield of oils was of 11.03 ± 5.94% for fresh leaves, and 1.07 ± 0.27% for dry leaves. The analysis showed 36 volatile compounds from fresh leaves and 49 from dried leaves. Main constituents in EOs of both fresh and dried leaves from P. cachimboense were (E)-caryophyllene, germacrene-D, -amorfene, -cadinene and apiole.

Piper cachimboense é registrada apenas para a região amazônica do Brasil e Colômbia, e o objetivo deste estudo foi relatar, pela primeira vez, a composição fitoquímica dos óleos essenciais (OEs) desta espécie coletada na floresta amazônica, em Novo Progresso/PA, Brasil. Amostras de folhas foram submetidas a hidrodestilação em aparelho tipo Clevenger. A identificação química foi realizada por cromatografia gasosa e o rendimento dos óleos foi de 11,03 ± 5,94% para as folhas frescas e de 1,07 ± 0,27% para as folhas secas. A análise mostrou 36 compostos voláteis para folhas frescas e 49 para folhas secas. Os constituintes principais dos OEs de folhas frescas e secas de P. cachimboense foram (E)-cariofileno, germacreno-D, -amorfeno, -cadineno e apiol.

Composição química do óleo essencial de duas amostras de carqueja (Baccharis sp. ) coletadas em Paty do Alferes - Rio de Janeiro / Chemical composition of essential oil from two samples of carqueja (Baccharis sp. ) collected in Paty do Alferes - Rio de Janeiro, Brazil

O Brasil possui em sua flora a maior diversidade genética do mundo, apresentando varias espécies nativas. Dentre as plantas nativas do Brasil encontra-se o gênero Baccharis (família Asteraceae) que possui algumas espécies popularmente conhecidas como carqueja, carqueja amarga ou vassoura. Estas espécies são utilizadas na medicina popular como protetora e estimulante do fígado, para o controle da obesidade, diabetes, hepatite, gastroenterite, digestiva, diurética, depurativa, tônica, antianêmica e anti-reumática. Este trabalho teve por objetivo investigar a composição química do óleo essencial de duas populações do gênero Baccharis coletadas em Paty do Alferes, visando encontrar novas fontes de carquejol e acetato de carquejila. Amostras de duas populações diferentes de carqueja foram coletadas em propriedades particulares Paty do Alferes - Rio de Janeiro em novembro de 2010. Estas foram secas a temperatura ambiente (28ºC +- 2) e à sombra. O óleo essencial das duas amostras de Baccharis sp. foi extraído por hidrodestilação em aparelho tipo Clevenger modificado durante 4 horas. O mesmo foi analisado por cromatografia gasosa acoplada à espectrômetro de massas (CG-EM Shimadzu, QP 5050, coluna capilar DB-5 - 30 m x 0.25µm x 0.25mm). Utilizou-se o Helio como gás carreador (1.7mL/min); temperatura do injetor: 240ºC e detector: 230ºC, Split: 1:20, no seguinte programa de temperatura: 60º C - 240º C (3ºC/ min). A identificação da composição química dos óleos essenciais foi realizada pela comparação de seus espectros de massa e valores de índice de Kovats (IK) com compostos conhecidos descritos na literatura. Foram identificados 19 compostos nestes óleos essenciais. Os principais compostos encontrados foram trans-cariofileno (22,0 por cento e 18,1 por cento), seguido por germacreno-D (7,0 por cento), biciclogermacreno (8,5 por cento), ledol (13,7 por cento), espatulenol (13,8 por cento e 20,7 por cento) e óxido de cariofileno (8,3 por cento e 12,0 por cento). Carquejol e acetato de carquejila não foram observados nestas amostras de óleo essencial, o que pode ser um indicativo que esta espécie não é B. trimera. Os resultados apresentados apontaram que as amostras coletadas em Paty do Alferes apresentam composição química similar e podem ser a mesma espécie vegetal, com grande indicativo de ser B. crispa (B cylindrica).

Brazil presents the highest vegetable genetic diversity of the world. Among the native plants of Brazil is some species of genus Baccharis (Asteraceae family) and popularly known as "carqueja". This medicinal specie has been used as diuretic, tonic, digestive, protective and stimulate of the liver, antianemic, anti-rheumatic, obesity control, diabetes, hepatitis and gastroenteritis. Samples of two different populations of plants were collected in a privet property in Paty do Alferes district (Rio de Janeiro State) in 11/2010, and dried at room temperature (28ºC +- 2) at shade conditions. Essential oil was extracted by hydrodistillation (Clevenger-type apparatus) for 4h and analyzed by GC-MS (Shimadzu, QP 5050-DB-5 capillary column - 30mx0.25µmx0.25mm). Carrier gas was Helium (1.7mL/min); split ratio: 1:30. Temperature program: 60º C - 240º C (3ºC/ min), rising to 240ºC at 3ºC/min. Injector temperature: 240ºC and detector temperature: 230ºC. Identifications of chemical compounds were made by matching their mass spectra and Kovat's indices (IK) values with known compounds reported in the literature. Were found 19 compounds in these essential oils. The major compound founded was trans-caryophyllene (22.0 percent and 18.1 percent), followed by germacrene-D (7.0 percent), bicyclogermacrene (8.5 percent), ledol (13.7 percent), spathulenol (13.8 percent and 20.7 percent) and caryophyllene oxide (8.3 percent and 12.0 percent). Carquejol and carquejyl acetate were not observed in these essential oil. These results showed that these samples present similar chemical composition and they can be the same vegetal specie (B. crispa/ B cylindrica).

Composição química do óleo volátil de Myrcianthes nativas da região sul do Brasil / Chemical composition of the volatile oils of native Myrcianthes species from South Brazil

O óleo essencial das folhas de Myrcianthes gigantea (Myrtaceae), coletadas no Rio Grande do Sul, foi obtido por hidrodestilação em Clevenger e analisado por CG/detector de ionização de chamas e CG/EM. Trinta e seis compostos foram identificados, totalizando 90,1 por cento do conteúdo do óleo. A composição do óleo demonstrou predominância de sesquiterpenos cíclicos, principalmente da via de ciclização do germacrano, apresentando espatulenol (28,8 por cento) e seu isômero, iso-espatulenol (9,5 por cento), como principais constituintes. A composição do óleo das folhas de M. cisplatensis e M. pungens, coletadas na mesma região, também foi analisada e comparada com estudos prévios reportados para estas espécies coletadas em outros países da América da Sul. O óleo essencial de M. cisplatensis apresentou um alto conteúdo de monoterpenos (56,3 por cento), especialmente das séries pinano e p-mentano, com três compostos majoritários: 1,8-cineol (29,8 por cento), limoneno (10,9 por cento) e a-pineno (8,9 por cento), sendo similar ao reportado. Para o óleo de M. pungens 36 compostos foram identificados, porém sem predomínio majoritário, onde b-cariofileno (10,1 por cento), foi o principal deles. O óleo desta espécie difere do relatado para exemplares coletados na Argentina, rico em monoterpenos, sugerindo uma possível ocorrência de quimiotipos.

The essential oil of Myrcianthes gigantea (Myrtaceae) leaves, which were collected in Rio Grande do Sul (Southern Brazil), was obtained by hydrodistillation in a Clevenger apparatus. The chemical investigation was performed by GC-FID and GC-MS. Thirty-six compounds were identified accounting for 90.1 percent of the oil content. The analyzed species was rich in cyclic sesquiterpenes, mainly those from the germecrane cyclization pathway, among them spathulenol (28.8 percent) and its isomer, iso-spathulenol (9.5 percent). Leaves of M. cisplatensis and M. pungens were also collected in the same region and the analysis of the oil composition was compared with those previously reported for collections from other countries in South America. M. cisplatensis oil showed a high content of monoterpenes (56.3 percent), specially from the p-mentane and pinane groups, with three major compounds: 1,8-cineole (29.8 percent), limonene (10.9 percent) and a-pinene (8.9 percent). These findings are in agreement with those reported previously. For M. pungens, thirty-six compounds were identified without a predominant component. b-caryophyllene (10.1 percent), with caryophyllane skeleton, was the main substance for this sample. For this species the oil composition was quite different from those related for two exemplars collected in Argentina, in which both oil were rich in monoterpenes. This result suggests the occurrence of chemotypes.