RESUMEN
Aphids are agricultural pest insects that transmit viruses and cause feeding damage on a global scale. Current pest control practices involving the excessive use of synthetic insecticides over many years have resulted in aphid resistance to a number of pesticides. In nature, plants produce secondary metabolites during their interaction with insects and these metabolites can act as toxicants, antifeedants, anti-oviposition agents and deterrents towards the insects. In a previous study, we demonstrated that the butanol fraction from a crude methanolic extract of an important plant species, Isodon rugosus showed strong insecticidal activity against the pea aphid, Acyrthosiphon pisum. To further explore this finding, the current study aimed to exploit a bioactivity-guided strategy to isolate and identify the active compound in the butanol fraction of I. rugosus. As such, reversed-phase flash chromatography, acidic extraction and different spectroscopic techniques were used to isolate and identify the new compound, rosmarinic acid, as the bioactive compound in I. rugosus. Insecticidal potential of rosmarinic acid against A. pisum was evaluated using standard protocols and the data obtained was analyzed using qualitative and quantitative statistical approaches. Considering that a very low concentration of this compound (LC90 = 5.4 ppm) causes significant mortality in A. pisum within 24 h, rosmarinic acid could be exploited as a potent insecticide against this important pest insect. Furthermore, I. rugosus is already used for medicinal purposes and rosmarinic acid is known to reduce genotoxic effects induced by chemicals, hence it is expected to be safer compared to the current conventional pesticides. While this study highlights the potential of I. rugosus as a possible biopesticide source against A. pisum, it also provides the basis for further exploration and development of formulations for effective field application.
Asunto(s)
Cinamatos/farmacología , Depsidos/farmacología , Insecticidas/farmacología , Isodon/química , Animales , Áfidos/efectos de los fármacos , Butanoles/aislamiento & purificación , Cinamatos/química , Depsidos/química , Insecticidas/química , Estructura Molecular , Pisum sativum/parasitología , Extractos Vegetales/aislamiento & purificación , Ácido RosmarínicoRESUMEN
The present study reveals that supplementing sodium acetate (NaAc) strongly stimulates riboflavin production in acetone-butanol-ethanol (ABE) fermentation by Clostridium acetobutylicum ATCC 824 with xylose as carbon source. Riboflavin production increased from undetectable concentrations to â¼0.2 g L-1 (0.53 mM) when supplementing 60 mM NaAc. Of interest, solvents production and biomass yield were also promoted with fivefold acetone, 2.6-fold butanol, and 2.4-fold biomass adding NaAc. A kinetic metabolic model, developed to simulate ABE biosystem, with riboflavin production, revealed from a dynamic metabolic flux analysis (dMFA) simultaneous increase of riboflavin (ribA) and GTP (precursor of riboflavin) (PurM) synthesis flux rates under NaAc supplementation. The model includes 23 fluxes, 24 metabolites, and 72 kinetic parameters. It also suggested that NaAc condition has first stimulated the accumulation of intracellular metabolite intermediates during the acidogenic phase, which have then fed the solventogenic phase leading to increased ABE production. In addition, NaAc resulted in higher intracellular levels of NADH during the whole culture. Moreover, lower GTP-to-adenosine phosphates (ATP, ADP, AMP) ratio under NaAc supplemented condition suggests that GTP may have a minor role in the cell energetic metabolism compared to its contribution to riboflavin synthesis.
Asunto(s)
Acetona/metabolismo , Butanoles/metabolismo , Clostridium acetobutylicum/metabolismo , Etanol/metabolismo , Análisis de Flujos Metabólicos/métodos , Riboflavina/biosíntesis , Acetato de Sodio/metabolismo , Acetona/aislamiento & purificación , Reactores Biológicos/microbiología , Butanoles/aislamiento & purificación , Clostridium acetobutylicum/crecimiento & desarrollo , Simulación por Computador , Medios de Cultivo/metabolismo , Etanol/aislamiento & purificación , Fermentación , Modelos Biológicos , Riboflavina/aislamiento & purificaciónRESUMEN
ETHNOPHARMACOLOGICAL RELEVANCE: Preparations of Olax subscorpioidea have been used traditionally for the management of pains, inflammatory diseases, yellow fever, cancer and rheumatism. Previously, the analgesic activity of its leaf extract have been reported. Furthermore, an analgesic assay guided fractionation showed that the butanol soluble fraction is the most active. However, the mechanism of this activity remains to be elucidated. This present study investigated the possible pharmacological mechanisms involved in the analgesic activity of the butanol leaf fraction of Olax subscorpioidea (BFOS) using the acetic acid induced writhing test in mice. MATERIALS AND METHODS: Animals were orally administered distilled water (10ml/kg), BFOS (1,000mg/kg) and morphine (10mg/kg) 60minutes before i.p administration of acetic acid and the resulting writhing were counted for 10minutes. To establish the possible mechanism(s) of action of BFOS, separate group of animals were pretreated with naloxone (2mg/kg, i.p), prazosin (1mg/kg, i.p), yohimbine (1mg/kg, i.p), propranolol (20mg/kg, i.p), metergoline (2mg/kg, i.p), glibenclamide (5mg/kg, i.p) and l-arginine (50mg/kg, i.p) 15minutes before BFOS. RESULTS: BFOS and morphine showed marked analgesic activities (p<0.001); the pretreatment of animals with naloxone, metergoline and l-arginine significantly (p<0.05 and p<0.001) reduced the analgesic activity of BFOS; however, pretreatment with prazosin, yohimbine, propranolol and glinbenclamide showed no effect on its analgesic activity. CONCLUSION: Results obtained in this study suggest the involvement of opioidergic, serotonergic and nitric oxide-l-arginine pathways in the analgesic effect of butanol leaf fraction of Olax subscorpioidea.
Asunto(s)
Analgésicos/farmacología , Butanoles/farmacología , Olacaceae , Dimensión del Dolor/efectos de los fármacos , Extractos Vegetales/farmacología , Hojas de la Planta , Analgésicos/aislamiento & purificación , Animales , Butanoles/aislamiento & purificación , Femenino , Masculino , Ratones , Dimensión del Dolor/métodos , Extractos Vegetales/aislamiento & purificaciónRESUMEN
Rhizomes of Zingiber cassumunar have been used for many years in traditional Thai medicine as an anti-inflammatory agent. The major bioactive component of this plant is Compound D [E-4-(3', 4'-dimethoxyphenyl)but-3-en-1-ol], which is a strong smooth muscle relaxant, and has antihistamine and anti-inflammatory actions. There is, however, incomplete information available for the pharmacokinetics of Compound D in mammals. In this study, we examined the pharmacokinetic profiles of Compound D in male Wistar rats. A standardized extract of Z. cassumunar containing 4â% w/w Compound D was administered intravenously at 25 mg/kg or by oral gavage at 25, 75, or 250 mg/kg to Wistar rats. Blood, tissues, urine, and feces were collected from 0 to 48 h after dosing and the level of Compound D was determined by liquid chromatography-tandem mass spectrometry. The concentration of Compound D ranged from 10-100 µg/L, reached a maximum approximately 0.15 h after oral dosing. Compound D exhibited an excellent tissue to plasma ratio, ranging from 1- to 1000 in several organs at 1-4 h after oral dosing. Less than 1â% of unchanged Compound D was excreted in the urine and feces. Further studies on tissue uptake and metabolite identification are required to obtain complete pharmacokinetic information and to develop appropriate dosing strategies of Compound D and the standardized extract of Z. cassumunar.
Asunto(s)
Butanoles/farmacocinética , Parasimpatolíticos/farmacocinética , Extractos Vegetales/farmacocinética , Zingiberaceae/química , Animales , Butanoles/química , Butanoles/aislamiento & purificación , Masculino , Estructura Molecular , Parasimpatolíticos/aislamiento & purificación , Parasimpatolíticos/orina , Extractos Vegetales/química , Ratas , Ratas Wistar , TailandiaRESUMEN
Sugar beet pulp (SBP) has been investigated as a promising feedstock for ABE fermentation by Clostridium beijerinckii. Although lignin content in SBP is low, a pretreatment is needed to enhance enzymatic hydrolysis and fermentation yields. Autohydrolysis at pH 4 has been selected as the best pretreatment for SBP in terms of sugars release and acetone and butanol production. The best overall sugars release yields from raw SBP ranged from 66.2% to 70.6% for this pretreatment. The highest ABE yield achieved was 0.4g/g (5.1g/L of acetone and 6.6g/L butanol) and 143.2g ABE/kg SBP (62.3g acetone and 80.9g butanol) were obtained when pretreated SBP was enzymatically hydrolyzed at 7.5% (w/w) solid loading. Higher solid loadings (10%) offered higher acetone and butanol titers (5.8g/L of acetone and 7.8g/L butanol). All the experiments were carried out under not-controlling pH conditions reaching about 5.3 in the final samples.
Asunto(s)
Acetona/metabolismo , Beta vulgaris/microbiología , Butanoles/metabolismo , Clostridium beijerinckii/metabolismo , Etanol/metabolismo , Extractos Vegetales/metabolismo , Acetona/aislamiento & purificación , Beta vulgaris/química , Biodegradación Ambiental , Reactores Biológicos/microbiología , Butanoles/aislamiento & purificación , Etanol/aislamiento & purificación , Hidrólisis , Extractos Vegetales/químicaRESUMEN
BACKGROUND: House dust mite (HDM) induced matrix metalloproteinase (MMP)-9 plays a role in asthma. Zingiber cassumunar Roxb. (Phlai in Thai) has been used in folk medicine for asthma treatment. OBJECTIVE: We investigated effects of Phlai and its constituent (E)-4-(3',4'-dimethoxyphenyl)but-3-en-1-ol (compound D) on the cleavage of pro- MMP-9 by HDM. The effects of these compounds on phorbol 12-myristate 13-acetate (PMA)- induced MMP-9 gene and protein expression in airway epithelial cells (NCI-H292) were also investigated. METHODS: Pro-MMP-9 was directly activated in vitro with HDM in the presence or absence of the ethanolic extracts of Phlai or compound D for 1 hour. The amount of activated MMP-9 was determined using gelatin zymography. To study the cellular response of Phlai, NCI-H292 cells were pretreated with crude Phlai extracts or compound D for 2 hours, and then the cells were stimulated with PMA for 48 hours. The mRNA RT-PCR and Western blotting, respectively. MMP-9 activity was determined by gelatin zymography. RESULTS: Crude Phlai extracts (0.25 - 2.0 mg/ml) and compound D (0.5 - 4.0 mg/ml) inhibited pro- MMP-9 cleavage by HDM. Furthermore, crude Phlai extracts (100 mg/ml) and compound D, at concentrations of 50 and 100 mg/ml, attenuated the PMA-induced MMP-9 gene and expression in NCI-H292 cells. These compound also suppressed MMP-9 release from PMA-induced NCI-H292 cells. CONCLUSION: The crude ethanolic extract of Z. cassumunar and its active constituent compound D inhibited the cleavage of pro-MMP-9 by HDM. They also inhibited PMA-induced MMP-9 gene and protein synthesis in human airway epithelial cells.
Asunto(s)
Antígenos Dermatofagoides/farmacología , Proteínas de Artrópodos/farmacología , Butanoles/farmacología , Cisteína Endopeptidasas/farmacología , Células Epiteliales/efectos de los fármacos , Metaloproteinasa 9 de la Matriz/metabolismo , Extractos Vegetales/farmacología , Pyroglyphidae/química , Zingiberaceae/química , Animales , Antígenos Dermatofagoides/aislamiento & purificación , Proteínas de Artrópodos/aislamiento & purificación , Butanoles/aislamiento & purificación , Línea Celular Tumoral , Cisteína Endopeptidasas/aislamiento & purificación , Activación Enzimática/efectos de los fármacos , Precursores Enzimáticos/genética , Precursores Enzimáticos/metabolismo , Células Epiteliales/citología , Células Epiteliales/metabolismo , Expresión Génica , Humanos , Metaloproteinasa 9 de la Matriz/genética , Ésteres del Forbol/farmacología , Preparaciones de Plantas/química , Mucosa Respiratoria/citología , Mucosa Respiratoria/efectos de los fármacos , Mucosa Respiratoria/metabolismoRESUMEN
A bioassay-guided purification of an EtOAc extract of the leaves of Croton mauritianus using a chikungunya virus-cell-based assay led to the isolation of 12-O-decanoylphorbol-13-acetate (1) and the new 12-O-decanoyl-7-hydroperoxy-phorbol-5-ene-13-acetate (2), along with loliolide, vomifoliol, dehydrovomifoliol, annuionone D and bluemol C. The planar structure and the relative configuration of compound 2 were elucidated based on spectroscopic analysis, including 1D- and 2D-NMR experiments, mass spectrometry, and comparison with literature data. Compounds 1 and 2 inhibited chikungunya virus-induced cell death in cell culture with EC50s of 2.4±0.3 and 4.0±0.8 µM, respectively.
Asunto(s)
Antivirales/aislamiento & purificación , Virus Chikungunya/efectos de los fármacos , Croton/química , Norisoprenoides/aislamiento & purificación , Ésteres del Forbol/aislamiento & purificación , Antivirales/química , Antivirales/farmacología , Benzofuranos/aislamiento & purificación , Benzofuranos/farmacología , Butanoles/aislamiento & purificación , Butanoles/farmacología , Ciclohexanonas/aislamiento & purificación , Ciclohexanonas/farmacología , Diterpenos/química , Diterpenos/aislamiento & purificación , Diterpenos/farmacología , Pruebas de Sensibilidad Microbiana , Norisoprenoides/farmacología , Ésteres del Forbol/farmacología , Hojas de la Planta/química , Replicación Viral/efectos de los fármacosRESUMEN
The methanolic extract and its EtOAc-soluble fraction from the rhizomes of Zingiber cassumunar inhibited invasion of human fibrosarcoma HT 1080 cells. From the EtOAc-soluble fraction, eight new phenylbutanoids, cassumunols A-H, were isolated together with 30 known constituents. The structures of new phenylbutanoids were elucidated on the basis of chemical and physicochemical evidence. Principal constituents were examined the inhibitory effects on the invasion of HT 1080 cells. Among them, phlain I and III, (E)-1-(3,4-dimethoxyphenyl)buta-1,3-diene, (E)-1-(2,4,5-trimethoxyphenyl)buta-1,3-diene, and (-)-ß-sesquiphellandrene showed anti-invasion effects. Interestingly, (E)-1-(2,4,5-trimethoxyphenyl)buta-1,3-diene [inhibition (%) 46.8 ± 7.2 (p<0.05) at 30 µM] significantly inhibited the invasion, and only a weak cytotoxic effect was observed.
Asunto(s)
Butanoles/química , Extractos Vegetales/química , Zingiberaceae/química , Butanoles/aislamiento & purificación , Butanoles/toxicidad , Línea Celular Tumoral , Fibrosarcoma/tratamiento farmacológico , Humanos , Espectroscopía de Resonancia Magnética , Conformación Molecular , Invasividad Neoplásica/prevención & control , Neoplasias de Tejido Conjuntivo/tratamiento farmacológico , Extractos Vegetales/uso terapéutico , Extractos Vegetales/toxicidad , Rizoma/químicaRESUMEN
OBJECTIVE: To study the chemical constituents of Pharbitis purpurea. METHODS: The constituents were isolated by silica gel column chromatography, HPLC and recrystallization and their structures were elucidated on the basis of spectral analysis. RESULTS: Fourteen compounds were isolated and identified as daucosterol (1), umbelliferone (2), ursolic acid (3), N-p-hydroxy-cis-coumaroyltyramine (4), N-p-hydroxy-trans-coumaroyltyramine (5), N-cis-feruloyltyramine (6), N-trans-feruloyltyramine (7), (3R, 5R, 6S, 7E, 9S)-megastigman-5,6-epoxy-7-ene-3,9-diol (8), (6S,9R)-vomifoliol (9), (+)-syringaresinol (10), isovitexin (11), syringopicroside( 12), uricil (13), (6S,9R)-roseoside (14). CONCLUSION: Compounds 3, 8-2,14 are isolated from the genus for the first time.
Asunto(s)
Apigenina/aislamiento & purificación , Butanoles/aislamiento & purificación , Convolvulaceae/química , Ciclohexanonas/aislamiento & purificación , Triterpenos/aislamiento & purificación , Apigenina/química , Butanoles/química , Ciclohexanonas/química , Glicósidos/química , Glicósidos/aislamiento & purificación , Estructura Molecular , Plantas Medicinales/química , Sitoesteroles/química , Sitoesteroles/aislamiento & purificación , Triterpenos/química , Ácido UrsólicoRESUMEN
Two novel butanol rhamnopyranosides (1 and 2), along with nine known compounds (3-11), have been isolated from various non-polar and polar extracts of an Indian traditional herb, Euphorbia hirta. The structures of the new compounds were elucidated as n-butyl-1-O-beta-L-rhamnopyranoside (1) and n-butyl-1-O-alpha-L-rhamnopyranoside (2) by spectroscopic methods including IR, HR-FABMS, 1D and 2D NMR techniques.
Asunto(s)
Butanoles/aislamiento & purificación , Euphorbia/química , Glicósidos/aislamiento & purificación , Extractos Vegetales/aislamiento & purificación , Fraccionamiento Químico , India , Espectroscopía de Resonancia Magnética , Estructura Molecular , Ramnosa/químicaRESUMEN
Five compounds, huyouyisu (1), vomifoliol (2), isoferulic acid (3), 1,2,3-trihydroxyphenol (4) and p-hydroxy-phenol (5), were isolated from the peels of Citrus changshan-huyou Y. B. Chang for the first time by utilizing repeated column chromatography on silica gel. Among them, huyouyisu (1) is a new compound. The structure was elucidated by using 1D and 2D spectra.
Asunto(s)
Citrus/química , Fenoles/aislamiento & purificación , Butanoles/química , Butanoles/aislamiento & purificación , Cinamatos/química , Cinamatos/aislamiento & purificación , Ciclohexanonas/química , Ciclohexanonas/aislamiento & purificación , Estructura Molecular , Fenoles/química , Plantas Medicinales/químicaRESUMEN
OBJECTIVE: To investigate the chemical constituents of the red alga Gymnogongrus flabelliformis Harv. METHOD: Compounds were isolated by normal phase silica gel and Sephadex LH - 20 gel column chromatography and reverse phase HPLC. Their structures were elucidated by spectroscopic methods including MS, 1H-NMR, 13C-NMR. Cytotoxicity of the compounds was screened by using standard MIT method. RESULT: Five compounds were isolated from G. flabelliforrmis, their structures were identified as(3S, 6R, 7E)-( + )-3-hydroxyl-4, 7-mega-stigmadien-9-one (1), (3S, 5R, 6S, 7E)-(-)-3-hydroxy-5, 6-epoxy-7-megastigmene-9-one (2), (3S, 5S, 6R, 7E)-(+)3-hydroxy-5, 6-epoxy-7-megastigmene-9-one (3), dehydrovomifoliol (4), (3R)-(-)4-[(2R, 4S)-4-acetoxy-2-hydroxy-2, 6, 6-trimethylcyclohexylidene] -3-buten-2-one (5). CONCLUSION: All of the compounds were obtained from this species for the first time and compound 1 was a new natural product. These compounds were inactive (IC50 > 10 microg x mL(-1)) in the MTT assay against several human cancer cell lines.
Asunto(s)
Butanoles/aislamiento & purificación , Ciclohexanonas/aislamiento & purificación , Norisoprenoides/aislamiento & purificación , Rhodophyta/química , Antineoplásicos/química , Antineoplásicos/aislamiento & purificación , Antineoplásicos/farmacología , Butanoles/química , Butanoles/farmacología , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Cromatografía Líquida de Alta Presión , Ciclohexanonas/química , Ciclohexanonas/farmacología , Humanos , Concentración 50 Inhibidora , Espectroscopía de Resonancia Magnética , Norisoprenoides/química , Norisoprenoides/farmacologíaRESUMEN
OBJECTIVE: To study the chemical constituents from n-butanol extracts of Periploca calophylla. METHOD: The constituents were isolated and purified by chromatographic technology and their structures were elucidated on the basis of physicochemical property and spectroscopic methods. RESULT: Eight glycosides were isolated and identified as periplocin (I), kaempferol 3-alpha-D-arabinoside (II), kaempferol 3-O-beta-D-glucoside (III), 3',4',5,7-tetrahydroxyflavanone-2(S)-3'-O-beta-D-glucopyranoside (IV), (+)-syringaresinol-4'-O-beta-D-monoglucoside (V), 1-sinapoylglucoside (VI), erigeside C (VII), 2,6-dimethoxy-4-hydroxyphenol 1-O-beta-D-glucoside (VIII). CONCLUSION: All the compounds were isolated for the first time from this plant.
Asunto(s)
Arabinosa/análogos & derivados , Arabinosa/aislamiento & purificación , Glicósidos/química , Quempferoles/aislamiento & purificación , Periploca/química , Plantas Medicinales/química , Saponinas/aislamiento & purificación , Arabinosa/química , Butanoles/química , Butanoles/aislamiento & purificación , Quempferoles/química , Rizoma/química , Saponinas/químicaRESUMEN
This study aimed to elucidate the anti-inflammatory and related activities of mushroom Phellinus linteus. The results show that the EtOH extract of Phellinus linteus (PLE) dose-dependently inhibited the mouse ear edema induced by croton oil. Among PLE subfractions, the n-BuOH subfraction showed highest anti-inflammatory activity in croton oil-induced ear edema test. The n-BuOH subfraction also showed highest inhibitory activity on the chick embryo chorioallantoic membrane (CAM) angiogenesis in a dose-dependent manner. PLE could significantly reduce the number of writhing induced by acetic acid in mice, indicating that PLE possesses potent antinociceptive effect mediated by its anti-inflammatory activity. Mycelial extract of six different Phellinus strains were found to contain anti-angiogenic activity in the CAM assay. These results suggest that Phellinus linteus has anti-inflammatory and antinociceptive activities, in addition to its anti-angiogenic activity.
Asunto(s)
Agaricales , Antiinflamatorios no Esteroideos/uso terapéutico , Butanoles/uso terapéutico , Edema/tratamiento farmacológico , Animales , Antiinflamatorios no Esteroideos/aislamiento & purificación , Butanoles/aislamiento & purificación , Embrión de Pollo , Relación Dosis-Respuesta a Droga , Masculino , Ratones , Ratones Endogámicos ICR , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/uso terapéuticoRESUMEN
Three antiinflammatory saponin components were isolated from the alkaline hydrolysate of a butanol-soluble portion of Kalopanax pictus bark extract through an in vivo activity-guided fractionation procedure. The hydrolysate showed inhibition of adjuvant induced arthritis in rats. After further fractionation, the ethyl acetate fraction exhibited antiarthritic activity, which resulted in the isolation of alpha-hederin, alpha-hederin methyl ester, and kalopanaxsaponin I. All compounds showed inhibition of vascular permeability in mice, but only alpha-hederin methyl ester showed anticarrageenan activity in rats and antiarthritic activity in rats and mice.
Asunto(s)
Antiinflamatorios no Esteroideos/aislamiento & purificación , Butanoles/aislamiento & purificación , Kalopanax , Ácido Oleanólico/análogos & derivados , Ácido Oleanólico/aislamiento & purificación , Saponinas/aislamiento & purificación , Animales , Antiinflamatorios no Esteroideos/química , Antiinflamatorios no Esteroideos/uso terapéutico , Artritis Experimental/inducido químicamente , Artritis Experimental/tratamiento farmacológico , Butanoles/química , Butanoles/uso terapéutico , Edema/inducido químicamente , Edema/tratamiento farmacológico , Ésteres , Hidrólisis , Masculino , Ácido Oleanólico/química , Ácido Oleanólico/uso terapéutico , Corteza de la Planta , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/uso terapéutico , Ratas , Ratas Sprague-Dawley , Saponinas/química , Saponinas/uso terapéuticoRESUMEN
The methanol extract of the dried roots of Rheum maximowiczii afforded four phenylbutanoid and two stilbene derivatives. Their structures were established on the basis of chemical and spectroscopic studies.
Asunto(s)
Butanoles/aislamiento & purificación , Plantas Medicinales/química , Polygonaceae/química , Estilbenos/aislamiento & purificación , Butanoles/química , Espectroscopía de Resonancia Magnética , Extractos Vegetales/química , Raíces de Plantas/química , Espectrometría de Masa Bombardeada por Átomos Veloces , Estilbenos/química , UzbekistánRESUMEN
AIM: To study the chemical constituents of the seeds from Artabotrys hexapetalus (L.f.) Bhandari (Annonaceae). METHODS: Various chromatographic techniques were used to separate and purify the constituents. Their structures were elucidated on the physico-chemical properties and spectral data. RESULTS: Eight compounds were isolated from the seeds of A. hexapetalus. They were identified as four neolignans: isoamericanin A (1), isoamericanol A (2), americanin B (3) and artabotrycinol (4), a semiterpenoid: (R)-artabotriol (5) and others: palmitic acid (6), beta-sitosterol (7) and daucosterol (8). CONCLUSION: Artabotrycinol (4) and (R)-artabotriol (5) are new compounds. Three other neolignans were isolated from this plant for the first time.
Asunto(s)
Annonaceae/química , Butanoles/aislamiento & purificación , Dioxanos/aislamiento & purificación , Plantas Medicinales/química , Butanoles/química , Dioxanos/química , Dioxinas/química , Dioxinas/aislamiento & purificación , Estructura Molecular , Semillas/químicaRESUMEN
The aim of this study was to investigate the effect of butanol fraction of the aqueous extract of Forsythia koreana fruits on the nitric oxide (NO) production and inducible nitric oxide synthesis (iNOS) gene expression in murine macrophage-like RAW 264.7 cells. Butanol fraction alone affected neither NO production nor iNOS gene expression in macrophage-like RAW 264.7 cells. However, the butanol fraction inhibited NO production and iNOS gene expression in RAW 264. 7 cells stimulated with interferon-gamma (IFN-gamma) and lipopolysaccharide (LPS). These findings suggest that inhibition of NO production by this butanol fraction in RAW 264.7 cells stimulated with IFN-gamma plus LPS was due to the suppression of iNOS gene expression.
Asunto(s)
Butanoles/farmacología , Macrófagos/efectos de los fármacos , Óxido Nítrico/biosíntesis , Extractos Vegetales/farmacología , Análisis de Varianza , Animales , Butanoles/aislamiento & purificación , Células Cultivadas , Interferón gamma/farmacología , Macrófagos/metabolismo , Ratones , Plantas MedicinalesRESUMEN
In this study, we investigated the effect of (+)-rhododendrol (1) and epi-rhododendrin (2) isolated from Acer nikoense Maxim. (Aceraceae) on nitric oxide (NO) production in mouse peritoneal macrophages elicited by bacillus Calmette-Guérin and in vitro stimulated by lipopolysaccharide. The NO production was not affected by an oral administration of methanol extract at a dose of 100 mg/kg/day. However, the AcOEt soluble fraction significantly reduced the NO production. (+)-Rhododendrol (1) isolated as an active substance from the AcOEt fraction suppressed the NO production. epi-Rhododendrin (2), the glucoside of (+)-rhododendrol (1) isolated from the n-BuOH fraction, also suppressed the NO production. As NO is one of the critical mediators in inflammation, these results suggest that (+)-rhododendrol (1) and epi-rhododendrin (2) contribute in part to the anti-inflammatory effect of A. nikoense.
Asunto(s)
Butanoles/farmacología , Macrófagos Peritoneales/efectos de los fármacos , Óxido Nítrico/antagonistas & inhibidores , Animales , Butanoles/química , Butanoles/aislamiento & purificación , Activación de Macrófagos , Macrófagos Peritoneales/metabolismo , Masculino , Ratones , Ratones Endogámicos ICR , Óxido Nítrico/biosíntesis , Plantas Medicinales/química , EstereoisomerismoRESUMEN
From the ethanol extract of Viscum coloratum (Kom.) Nakai, a glucoside of aliphatic diol and three other glucosides were isolated. Based on chemical and spectroscopic analysis, the structures have been elucidated as 2-beta-D-glucosyl-3-methylpropanol (VIII), syringin (IX), eleatheroside E (X) and syringenin-4'-O-D-apiosylglucoside (XI). VIII is a new glucoside of aliphatic diol and named 3-beta-D-glucopyranosyloxy-butanol-2. Three other compounds (IX-XI) were found for the first time in this plant.