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1.
J Microbiol Biotechnol ; 32(9): 1154-1167, 2022 Sep 28.
Artigo em Inglês | MEDLINE | ID: mdl-36039041

RESUMO

In this study, we investigated the anti-amnesic effect of Korean red pine (Pinus densiflora) bark extract (KRPBE) against amyloid beta1-42 (Aß1-42)-induced neurotoxicity. We found that treatment with KRPBE improved the behavioral function in Aß-induced mice, and also boosted the antioxidant system in mice by decreasing malondialdehyde (MDA) content, increasing superoxide dismutase (SOD) activities, and reducing glutathione (GSH) levels. In addition, KRPBE improved the cholinergic system by suppressing reduced acetylcholine (ACh) content while also activating acetylcholinesterase (AChE), regulating the expression of choline acetyltransferase (ChAT), postsynaptic density protein-95 (PSD-95), and synaptophysin. KRPBE also showed an ameliorating effect on cerebral mitochondrial deficit by regulating reactive oxygen species (ROS), mitochondrial membrane potential (MMP) and ATP levels. Moreover, KRPBE modulated the expression levels of neurotoxicity indicators Aß and phosphorylated tau (p-tau) and inflammatory cytokines TNF-α, p-IκB-α, and IL-1ß. Furthermore, we found that KRPBE improved the expression levels of neuronal apoptosis-related markers BAX and BCl-2 and increased the expression levels of BDNF and p-CREB. Therefore, this study suggests that KRPBE treatment has an anti-amnestic effect by modulating cholinergic system dysfunction and neuroinflammation in Aß1-42-induced cognitive impairment in mice.


Assuntos
Disfunção Cognitiva , Fármacos Neuroprotetores , Pinus , Acetilcolina/metabolismo , Acetilcolina/farmacologia , Acetilcolinesterase/metabolismo , Trifosfato de Adenosina/metabolismo , Peptídeos beta-Amiloides , Animais , Antioxidantes/farmacologia , Fator Neurotrófico Derivado do Encéfalo/metabolismo , Colina O-Acetiltransferase/metabolismo , Colina O-Acetiltransferase/farmacologia , Colinérgicos/farmacologia , Disfunção Cognitiva/induzido quimicamente , Disfunção Cognitiva/tratamento farmacológico , Glutationa/metabolismo , Malondialdeído/metabolismo , Malondialdeído/farmacologia , Camundongos , Inibidor de NF-kappaB alfa/metabolismo , Doenças Neuroinflamatórias , Fármacos Neuroprotetores/farmacologia , Estresse Oxidativo , Casca de Planta , Extratos Vegetais/farmacologia , Espécies Reativas de Oxigênio/metabolismo , República da Coreia , Superóxido Dismutase/metabolismo , Sinaptofisina/metabolismo , Sinaptofisina/farmacologia , Fator de Necrose Tumoral alfa/metabolismo , Proteína X Associada a bcl-2/metabolismo
2.
J Econ Entomol ; 112(4): 1752-1759, 2019 08 03.
Artigo em Inglês | MEDLINE | ID: mdl-31009531

RESUMO

Matsuone is a well-known sex pheromone of the genus Matsucoccus (Hemiptera: Margarodidae), including species Matsucoccus matsumurae (Kuwana), Matsucoccus resinosae Bean & Goldwin, and Matsucoccus thunbergianae Miller & Park. In this study, we investigated the effects of matsuone dose and trap height on the capture of M. thunbergianae and developed an alternative synthesis of racemic matsuone. In field trapping experiments, M. thunbergianae males showed dose-dependent attraction to (6R,10R/S)-matsuone from 100 µg up to an approximate saturation level of 1,600 µg per rubber septum lure. Traps baited with (6R,10R/S)-matsuone and installed 50 cm above ground level attracted more males than traps 100 and 150 cm above ground level. To reduce synthesis procedures, time, and labor, we developed a new synthetic route to racemic matsuone and conducted field experiments with the product. Although traps baited with the racemic matsuone were less attractive than traps baited with (6R,10R/S)-matsuone synthesized by a previously reported method, the new synthetic route could be an economically favorable alternative to the previous method used in production of lures for field application.


Assuntos
Hemípteros , Pinus , Atrativos Sexuais , Animais , Controle de Insetos , Masculino , Feromônios
3.
J Econ Entomol ; 111(4): 1768-1774, 2018 08 03.
Artigo em Inglês | MEDLINE | ID: mdl-29788181

RESUMO

We confirmed an aggregation-sex pheromone of the Korean Monochamus alternatus Hope (Coleoptera: Cerambycidae) population, which primarily transmitted the pine wood nematode in Korea. Only the M. alternatus male emitted monochamol which has been previously reported in the Chinese M. alternatus population. In field attraction testing, the monochamol+α-pinene+ethanol combination attracted more M. alternatus adult beetles than traps containing only monochamol, ethanol, or α-pinene. The bark beetle aggregation pheromone compounds of ipsenol, ipsdienol, and ipsenol+ipsdienol, did not show synergistic effects with the monochamol+α-pinene+ethanol combination. No synergistic effects were observed when each host volatile compound of 3-carene, ß-caryophyllene, limonene, myrcene, and ß-pinene was added to traps containing monochamol+α-pinene+ethanol. The ratio of female beetles was much higher in traps containing the monochamol+α-pinene+ethanol combination than that of the natural population. Our results indicated that pheromone and synergists could be useful for managing the M. alternatus population.


Assuntos
Besouros , Pinus , Atrativos Sexuais , Animais , Feminino , Masculino , Feromônios , República da Coreia
4.
J Econ Entomol ; 111(2): 653-661, 2018 04 02.
Artigo em Inglês | MEDLINE | ID: mdl-29474548

RESUMO

The insecticidal activities of 13 Lamiaceae plant oils and their components against adult German cockroaches, Blattella germanica L. (Blattodea: Blattellidae), were evaluated using fumigant and contact bioassay. Among the tested oils, basil, pennyroyal, and spearmint showed the strongest insecticidal activities against adult B. germanica. Insecticidal activity of pennyroyal was 100% against male B. germanica at 1.25 mg concentration in fumigant bioassay. Basil and spearmint revealed 100% and 100% insecticidal activity against male B. germanica at 5 mg concentration, but their activities reduced to 80% and 25% at 2.5 mg concentration, respectively. In contact, toxicity bioassay, basil, pennyroyal, and spearmint oils exhibited 100%, 100%, and 98% mortality against female B. germanica at 1 mg/♀, respectively. Among the constituents identified in basil, pennyroyal, and spearmint oils, insecticidal activity of pulegone was the strongest against male and female B. germanica.


Assuntos
Blattellidae , Inseticidas/isolamento & purificação , Lamiaceae/química , Óleos Voláteis , Animais , Feminino , Masculino , Testes de Toxicidade
5.
Molecules ; 22(9)2017 Sep 18.
Artigo em Inglês | MEDLINE | ID: mdl-28927023

RESUMO

Among 98 3-acyltetramic acid analogues, compounds 1c, 2c, 2f and 2g, showed >90% nematicidal activity against the pine wood nematode Bursaphelenchus xylophilus at a 10 µg/mL concentration. The nematicidal activities of compounds 1d, 1h, and 2k were a little lower at 88.0%, 85.8%, and 57.2% at a 10 µg/mL concentration, respectively. The nematicidal activity of emamection benzoate, widely used in Korea for the prevention of pine wilt disease, was 32.3% at a 10 µg/mL concentration. Other 3-acyltetramic acid analogues showed less than 30% nematicidal activity. A structure-activity relationship study indicated that the chain length of the C-acyl substituent was very important for high nematicidal activity. All active compounds had C13H27 or C11H23 acyl substituents, in two closely related groups with the common physicochemical properties of a polar surface area 57.6A², PSA (polar surface area) 7.8-8.6% and ClogP (calculated partition coefficient) 5.1-5.9 and a polar surface area 75-84A², PSA 11.1-11.6% and ClogP 4.7-5.1, respectively. Our study indicates that active 3-acyltetramic acid analogues could have potential as lead compounds for developing novel pine wood nematode control agents.


Assuntos
Antinematódeos/química , Pirrolidinonas/química , Tylenchida/efeitos dos fármacos , Animais , Antinematódeos/farmacologia , Estrutura Molecular , Pinus , Pirrolidinonas/farmacologia , Relação Estrutura-Atividade , Propriedades de Superfície
6.
J Chem Ecol ; 43(7): 670-678, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28689277

RESUMO

In this study, we isolated and identified an aggregation-sex pheromone from Monochamus saltuarius, the major insect vector of the pine wood nematode in Korea. Adult males of M. saltuarius produce 2-undecyloxy-1-ethanol, which is known as an aggregation-sex pheromone in other Monochamus species. We performed field experiments to determine the attractiveness of the pheromone and other synergists. More M. saltuarius adult beetles were attracted to traps baited with the pheromone than to unbaited traps. Ethanol and (-)-α-pinene interacted synergistically with the pheromone. Traps baited with the pheromone + (-)-α-pinene +ethanol were more attractive to M. saltuarius adults than traps baited with the pheromone, (-)-α-pinene, or ethanol alone. Ipsenol, ipsdienol, and limonene were also identified as synergists of the aggregation-sex pheromone for M. saltuarius adults. In field experiments, the proportion of females was much higher in the beetles caught in traps than among the beetles emerging from naturally-infested logs in the laboratory. Our results suggest that a combination of aggregation-sex pheromone and synergists could be very effective for monitoring and managing M. saltuarius.


Assuntos
Besouros/fisiologia , Etanol/análogos & derivados , Éteres/metabolismo , Controle de Insetos/métodos , Pinus/parasitologia , Doenças das Plantas/parasitologia , Atrativos Sexuais/metabolismo , Tylenchida/fisiologia , Animais , Comportamento Animal , Monoterpenos Bicíclicos , Besouros/química , Etanol/análise , Etanol/metabolismo , Éteres/análise , Feminino , Insetos Vetores/química , Insetos Vetores/fisiologia , Masculino , Monoterpenos/metabolismo , Atrativos Sexuais/análise
7.
Molecules ; 22(7)2017 Jul 17.
Artigo em Inglês | MEDLINE | ID: mdl-28714917

RESUMO

Widespread concern for the occurrence of resistant strains, along with the avoidance of the use of highly toxic insecticides and their wide environmental dispersal, highlights the need for the development of new and safer pest control agents. Natural products provide inspiration for new chemical entities with biological activities, and their analogues are good lead compounds for the development of new pest control agents. For this purpose, we evaluated the larvicidal and nematicidal activities of 48 3-acylbarbituric acid analogues against the Asian tiger mosquito, Aedes albopictus and the pine wood nematode, Bursaphelenchus xylophilus, organisms of increasing global concern. Among the 48 3-acylbarbituric acid analogues, four compounds-10, 14d, 14g and 19b-showed >90% larvicidal activity against Ae. albopictus at 10 µg/mL concentration, and one (compound 10) showed the strongest larvicidal activity against Ae. albopictus, with a LC50 value of 0.22 µg/mL. Only compound 18 showed strong nematicidal activity against pine wood nematode. Most active compounds possessed similar physicochemical properties; thus, actives typically had ClogP values of around 1.40-1.50 and rel-PSA values of 16-17% and these similar cheminformatic characteristics reflect their similar structure. This study indicates that active 3-acylbarbituric acids analogues have potential as lead compounds for developing novel mosquito control agents.


Assuntos
Aedes/efeitos dos fármacos , Antinematódeos/farmacologia , Toxinas Bacterianas/farmacologia , Barbitúricos/farmacologia , Cromadoria/efeitos dos fármacos , Inseticidas/farmacologia , Controle de Mosquitos , Animais , Antinematódeos/química , Toxinas Bacterianas/química , Barbitúricos/química , Inseticidas/química
8.
J Econ Entomol ; 110(2): 552-557, 2017 04 01.
Artigo em Inglês | MEDLINE | ID: mdl-28165121

RESUMO

We evaluated the repellent activity of 12 Apiaceae plant essential oils and their components against male and female adult German cockroaches, Blattella germanica L., to find new natural repellents. Of all the plant essential oils tested, ajowan (Trachyspermum ammi Sprague) and dill (Anethum graveolens L.) essential oils showed the most potent repellent activity against male and female adult German cockroaches. Repellent activities of chemicals already identified in active oils were also investigated. Of the compounds identified, carvacrol, thymol, and R-(-)-carvone showed >80% repellent activity against male and female adult German cockroaches at 2.5 µg/cm2. S-(+)-Carvone, (+)-dihydrocarvone, and terpinen-4-ol showed >70% repellent activity against male and female adult German cockroaches at 10 µg/cm2. Our results indicated that Apiaceae plant essential oils and their constituents have good potential as natural repellents against adult German cockroaches.


Assuntos
Apiaceae/química , Blattellidae/efeitos dos fármacos , Repelentes de Insetos/farmacologia , Óleos Voláteis/farmacologia , Óleos de Plantas/farmacologia , Animais , Repelentes de Insetos/análise , Repelentes de Insetos/química , Óleos Voláteis/análise , Óleos Voláteis/química , Óleos de Plantas/análise , Óleos de Plantas/química
9.
Molecules ; 21(3): 361, 2016 Mar 16.
Artigo em Inglês | MEDLINE | ID: mdl-26999084

RESUMO

To find a new and safe alternative to conventional insecticides, we evaluated the fumigant toxicity of eight Lamiaceae essential oils and their constituents against the adult rice weevil Sitophilus oryzae. Of the eight species tested, hyssop (Hyssopus offcinalis), majoram (Origanum majorana), and Thymus zygis essential oils showed strong fumigant toxicity against S. oryzae adults at 25 mg/L air concentration. Constituents of active essential oils were analyzed by gas chromatography coupled to flame ionization detector (FID) and gas chromatography-mass spectrometry. A total of 13, 15, and 17 compounds were identified from hyssop, majoram, and Thymus zygis essential oils, respectively. Pinocamphone and isopinocamphone were isolated by open column chromatography. Among the test compounds, pinocamphone and isopinocamphone showed the strongest fumigant toxicity against S. oryzae. Sabinene hydrate, linalool, α-terpineol, and terpinen-4-ol exhibited 100% fumigant toxicity against S. oryzae at 3.9 mg/L air concentration. The measured toxicity of the artificial blends of the constituents identified in hyssop, majoram, and Thymus zygis oils indicated that isopinocamphone, terpine-4-ol, and linalool were major contributors to the fumigant toxicity of the artificial blend, respectively.


Assuntos
Inseticidas/química , Inseticidas/toxicidade , Lamiaceae/química , Óleos Voláteis/química , Óleos Voláteis/toxicidade , Gorgulhos/efeitos dos fármacos , Animais , Fumigação , Cromatografia Gasosa-Espectrometria de Massas , Oryza/parasitologia
10.
J Agric Food Chem ; 63(45): 9977-86, 2015 Nov 18.
Artigo em Inglês | MEDLINE | ID: mdl-26500081

RESUMO

This study evaluated the larvicidal activity of 12 Apiaceae plant essential oils and their components against the Asian tiger mosquito, Aedes albopictus, and the inhibition of acetylcholine esterase with their components. Of the 12 plant essential oils tested, ajowan (Trachyspermum ammi), caraway seed (Carum carvi), carrot seed (Daucus carota), celery (Apium graveolens), cumin (Cuminum cyminum), dill (Anethum graveolens), and parsley (Petroselinum sativum) resulted in >90% larval mortality when used at 0.1 mg/mL. Of the compounds identified, α-phellandrene, α-terpinene, p-cymene, (-)-limonene, (+)-limonene, γ-terpinene, cuminaldehyde, neral, (S)-+-carvone, trans-anethole, thymol, carvacrol, myristicin, apiol, and carotol resulted in >80% larval mortality when used at 0.1 mg/mL. Two days after treatment, 24.69, 3.64, and 12.43% of the original amounts of the celery, cumin, and parsley oils, respectively, remained in the water. Less than 50% of the original amounts of α-phellandrene, 1,8-cineole, terpinen-4-ol, cuminaldehyde, and trans-antheole were detected in the water at 2 days after treatment. Carvacrol, α-pinene, and ß-pinene inhibited the activity of Ae. albopictus acetylcholinesterase with IC50 values of 0.057, 0.062, and 0.190 mg/mL, respectively. A spherical microemulsion of parsley essential oil-loaded poly(vinyl alcohol) (PVA) was prepared, and the larvicidal activity of this formulation was shown to be similar to that of parsley oil.


Assuntos
Aedes/enzimologia , Apiaceae/química , Inibidores da Colinesterase/farmacologia , Proteínas de Insetos/antagonistas & inibidores , Inseticidas/farmacologia , Larva/efeitos dos fármacos , Óleos Voláteis/farmacologia , Acetilcolinesterase/metabolismo , Aedes/efeitos dos fármacos , Aedes/crescimento & desenvolvimento , Animais , Química Farmacêutica , Inibidores da Colinesterase/química , Feminino , Proteínas de Insetos/metabolismo , Inseticidas/química , Larva/enzimologia , Larva/crescimento & desenvolvimento , Masculino , Óleos Voláteis/química
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