RESUMO
The aim of this study was to evaluate the in vitro insecticidal activity of the essential oil (EO) of P. cablin against immature and adult stages of C. felis. The chemical composition of P. cablin EO was determined by gas chromatography (GC). To evaluate the insecticidal activity, the egg, larva, pupa, and adult stages of C. felis were exposed to different concentrations of P. cablin EO diluted in acetone and impregnated in filter paper in a concentration range of 25 to 200 µg.cm-2. After exposure, the material was incubated in climatized chambers and mortality assessment was performed after 24 h for the larval and adult stages, 72 h for the egg stage and 15 days for the pupal stage. After GC analysis, the major constituents of the EO of P. cablin were found to be patchoulol (27.4%), α-bulnesene (19.7%) and α-guayene (15.0%). The of mortality percentage was 100% at the concentration of 200 µg.cm-2 for all stages. The LCs50 values were 46.1, 49.2, 60.6 and 62.7 µg.cm-2, respectively for the pupal, egg, larva and adult stages. Based on the results obtained, we can conclude that the EO of P. cablin contained patchoulol, α-bulnesene, and α-guayene as major constituents and had insecticidal activity against the immature and adult stages of C. felis.
O objetivo deste estudo foi avaliar a atividade inseticida in vitro do óleo essencial (OE) de Pogostemon cablin frente estágios imaturos e adultos de Ctenocephalides felis. A composição química do OE de P. cablin foi determinada por cromatografia gasosa (CG). Para a avaliação da atividade inseticida os estágios de ovo, larva, pupa e adultos de C. felis foram expostos a diferentes concentrações do OE de P. cablin diluídos em acetona e impregnados em papel filtro com a faixa de concentração de 25 a 200 µg.cm-2. Após a exposição, o material foi incubado em câmaras climatizadas e a avaliação da mortalidade foi realizada após 24 h para os estágios de larvas e adultos, 72 h para o estágio de ovo e 15 dias para o estágio de pupa. Após análise cromatográfica, os constituintes majoritários para o OE de P. cablin foram: patchoulol (27,4%), α-bulneseno (19,7%) e α-guaieno (15%). Foi obtido 100% de mortalidade na concentração de 200 µg.cm-2 para todos os estágios. As CLs50 foram de 46,1; 49,2; 60,6 e 62,7 µg.cm-2, respectivamente para os estágios de pupa, ovo, larva e adultos. Com base nos resultados obtidos é possível concluir que o OE de P. cablin apresentou o patchoulol, α-bulneseno, e α-guaieno como constituintes majoritários e atividade inseticida frente aos estágios imaturos e adultos de C. felis.
RESUMO
Alzheimer's disease (AD), a progressive neurodegenerative disorder of the aged brain with no known cause or cures, has become a major medical and social problem for industrialized countries. Cerebral deposition of amyloid-ß peptide (Aß) is a critical feature of AD. The use of medicinal plants as an alternative form of prevention, or even as a possible treatment of AD, is therefore interesting areas of research. Sesquiterpene lactones and a sesquiterpene alcohol are compounds found in H. brasiliense that have several anti-oxidative and anti-inflammatory effects. In the present study, we investigated whether these compounds have neuroprotective effects in an amyloid-ß peptide-induced Alzheimer's disease mouse model. Mice were injected with Aß1-42 peptide intracerebroventricularly and were subsequently injected (i.c.v.) with 1µg/site of IGM-A (15-acetoxy-isogermafurenolide), IGM-H (15-hydroxy-isogermafurenolide), PDA (Podoandin), EHP (1,2-epoxy-10α-hydroxy-podoandin), HDS (13-hydroxy-8,9-dehydroshizukanolide), and ARD (aromadendrane-4ß,10α-diol). Seven days after treatments the animals had their memory tested in the inhibitory avoidance. After the behavioral testing of animals the brains were removed and subjected to biochemical tests for oxidative stress. The results showed that ARD, HDS and PDA significantly ameliorated the Aß1-42 peptide-induced memory impairment in the passive avoidance task (P<0.05). In addition, GSH activity was increased while the TBARS levels were decreased by treatment with these compounds. These results suggest that these compounds inhibit the cognitive deficit of animals induced peptide amyloid and may be potential candidates for Alzheimer's disease therapy.