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1.
Molecules ; 25(3)2020 Jan 29.
Artigo em Inglês | MEDLINE | ID: mdl-32013210

RESUMO

This paper reports the isolation and structural characterization of four new ent-kaurane derivatives from the Lamiaceae plant Sideritis hyssopifolia. Planar structures and relative configurations were determined using both mass spectrometry and nuclear magnetic resonance (1D and 2D). Absolute configurations were determined by comparing experimental and theoretical electronic circular dichroism spectra. The cytotoxic and microbial activities of all new compounds were tested. Compounds that were non-cytotoxic were further evaluated for anti-inflammatory activity.


Assuntos
Anti-Inflamatórios/farmacologia , Antineoplásicos/farmacologia , Diterpenos do Tipo Caurano/farmacologia , Extratos Vegetais/farmacologia , Sideritis/química , Anti-Inflamatórios/química , Anti-Inflamatórios/isolamento & purificação , Antineoplásicos/química , Antineoplásicos/isolamento & purificação , Linhagem Celular Tumoral , Diterpenos do Tipo Caurano/química , Diterpenos do Tipo Caurano/isolamento & purificação , Humanos , Modelos Moleculares , Estrutura Molecular , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Análise Espectral
2.
Molecules ; 23(5)2018 May 22.
Artigo em Inglês | MEDLINE | ID: mdl-29789477

RESUMO

Re-investigation of the chemical composition of the annual plant Mitracarpus scaber Zucc. led to the identification of clarinoside, a new pentalogin derivative containing a rare quinovose moiety, and the known compound harounoside. While the planar structure was fully determined using tandem mass spectrometry (MS) and quantum mechanics (QM) calculations, the tridimensional structure was unravelled after isolation and NMR analysis. The absolute configuration was assigned by comparison of experimental and theoretical synchrotron radiation circular dichroism spectra. Both compounds were tested for anti-inflammatory activity, and compound 1 showed the ability to inhibit the production of interleukin-8 (Il-8) with an IC 50 value of 9.17 µ M.


Assuntos
Anti-Inflamatórios/isolamento & purificação , Anti-Inflamatórios/farmacologia , Interleucina-8/metabolismo , Rubiaceae/química , Anti-Inflamatórios/química , Linhagem Celular , Dicroísmo Circular , Regulação para Baixo , Regulação da Expressão Gênica/efeitos dos fármacos , Humanos , Queratinócitos/citologia , Queratinócitos/efeitos dos fármacos , Queratinócitos/metabolismo , Extratos Vegetais/análise , Extratos Vegetais/farmacologia , Teoria Quântica , Síncrotrons , Espectrometria de Massas em Tandem , Fator de Necrose Tumoral alfa/farmacologia
3.
J Mass Spectrom ; 47(11): 1500-9, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23147829

RESUMO

Annonaceous acetogenins (AAGs) are a homogenous class of polyketides proposed as environmental neurotoxins. Previous dereplication studies of AAGs were limited by the use of low-resolution mass spectrometers. Only poor information in terms of structures was provided due to the limited fragmentation of protonated or sodium cationized species. An innovative approach, using reversed-phase high-performance liquid chromatography coupled to a hybrid linear ion trap/orbitrap mass spectrometer (LTQ-Orbitrap®), was therefore performed. Sensitivity was enhanced by post-column infusion of lithium, since AAGs have a high affinity for this cation. High level of structural information was obtained from low-energy-collision-induced dissociation fragmentation experiments of lithium-cationized AAGs ([M + Li](+) ions) as demonstrated with purified standards. The method was then applied to a total ethyl-acetate extract prepared from commercial soursop nectar (Annona muricata L.). The sensitivity, mass accuracy and specific fragmentation patterns proved to be particularly useful for characterization of the AAGs. Typical structural identification procedure and unexpected observations for specific structural types are illustrated, with major and minor compounds.


Assuntos
Acetogeninas/análise , Acetogeninas/química , Cromatografia Líquida de Alta Pressão/métodos , Lítio/química , Extratos Vegetais/química , Espectrometria de Massas por Ionização por Electrospray/métodos , Acetatos/química , Annona/química , Cátions/química , Cromatografia de Fase Reversa/métodos , Modelos Moleculares , Sensibilidade e Especificidade
4.
PLoS One ; 6(4): e18359, 2011 Apr 22.
Artigo em Inglês | MEDLINE | ID: mdl-21526169

RESUMO

BACKGROUND: The adult medicinal leech central nervous system (CNS) is capable of regenerating specific synaptic circuitry after a mechanical lesion, displaying evidence of anatomical repair within a few days and functional recovery within a few weeks. In the present work, spatiotemporal changes in molecular distributions during this phenomenon are explored. Moreover, the hypothesis that neural regeneration involves some molecular factors initially employed during embryonic neural development is tested. RESULTS: Imaging mass spectrometry coupled to peptidomic and lipidomic methodologies allowed the selection of molecules whose spatiotemporal pattern of expression was of potential interest. The identification of peptides was aided by comparing MS/MS spectra obtained for the peptidome extracted from embryonic and adult tissues to leech transcriptome and genome databases. Through the parallel use of a classical lipidomic approach and secondary ion mass spectrometry, specific lipids, including cannabinoids, gangliosides and several other types, were detected in adult ganglia following mechanical damage to connected nerves. These observations motivated a search for possible effects of cannabinoids on neurite outgrowth. Exposing nervous tissues to Transient Receptor Potential Vanilloid (TRPV) receptor agonists resulted in enhanced neurite outgrowth from a cut nerve, while exposure to antagonists blocked such outgrowth. CONCLUSION: The experiments on the regenerating adult leech CNS reported here provide direct evidence of increased titers of proteins that are thought to play important roles in early stages of neural development. Our data further suggest that endocannabinoids also play key roles in CNS regeneration, mediated through the activation of leech TRPVs, as a thorough search of leech genome databases failed to reveal any leech orthologs of the mammalian cannabinoid receptors but revealed putative TRPVs. In sum, our observations identify a number of lipids and proteins that may contribute to different aspects of the complex phenomenon of leech nerve regeneration, establishing an important base for future functional assays.


Assuntos
Hirudo medicinalis/metabolismo , Metabolismo dos Lipídeos , Regeneração Nervosa/fisiologia , Sistema Nervoso/metabolismo , Peptídeos/metabolismo , Sequência de Aminoácidos , Animais , Axotomia , Canabinoides/metabolismo , Cromatografia Líquida de Alta Pressão , Análise por Conglomerados , Embrião não Mamífero/metabolismo , Gânglios dos Invertebrados/metabolismo , Gânglios dos Invertebrados/patologia , Hirudo medicinalis/embriologia , Dados de Sequência Molecular , Sistema Nervoso/patologia , Peptídeos/química , Filogenia , Proteoma/metabolismo , Receptores de Canabinoides/genética , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Medula Espinal/metabolismo , Medula Espinal/patologia , Estresse Mecânico , Canais de Cátion TRPV/metabolismo , Fatores de Tempo
5.
Planta Med ; 74(12): 1457-62, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18671198

RESUMO

A significant acetylcholinesterase inhibitory activity was observed for the ethyl acetate and methanol extracts from the leaves and the fruits of MYRISTICA CRASSA. Three new dimeric acylphenols, giganteone C ( 5), maingayones B and C ( 6 and 7) were isolated together with the known malabaricones B and C ( 2 and 3) and giganteone A ( 4). Compounds 2 and 3 possess significant inhibitory activity on acetylcholinesterase. LC/MS study was particularly useful to discriminate structures of compounds 6 and 7.


Assuntos
Inibidores da Colinesterase/farmacologia , Myristicaceae/química , Fenóis/farmacologia , Inibidores da Colinesterase/química , Cromatografia Líquida de Alta Pressão , Espectrometria de Massas , Ressonância Magnética Nuclear Biomolecular , Fenóis/química , Fenóis/isolamento & purificação
6.
Anal Bioanal Chem ; 390(7): 1873-9, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18320177

RESUMO

Microsamples of pink cosmetic powders from the Greco-Roman period were analyzed using two complementary analytical approaches for identification of the colouring agents (lake pigments originally manufactured from madder plants with an inert binder, usually a metallic salt) present in the samples. The first technique was a methanolic acidic extraction of the archaeological samples with an additional ethyl acetate extraction of the anthraquinone-type colouring agents which were identified using high performance liquid chromatography coupled to electrospray ionization with high resolution mass spectrometry (LC-ESI-HRMS), and the second was direct analysis of a microsample by laser desorption ionization-mass spectrometry (LDI-MS). The latter technique is well suited when the quantity of samples is very low. This soft ionization technique enables the detection of very small quantities of compounds using the combination of positive and negative-ion modes. It was also successfully applied for the direct analysis of some laboratory-made reference compounds. However, the presence of lead in one of these ancient samples induced a spectral suppression phenomenon. In this case and conditional on a sufficient quantity of available sample, the former method is better adapted for the characterization of these anthraquinone-type molecules. This study also confirmed that purpurin, munjistin, and pseudopurpurin are the principal colouring agents present in these ancient cosmetic powders constituted from madder plants.


Assuntos
Cosméticos/análise , Pós/análise , Espectrometria de Massas por Ionização por Electrospray/métodos , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz/métodos , Arqueologia/métodos , Cromatografia Líquida de Alta Pressão/métodos , Mundo Grego , Estrutura Molecular , Extratos Vegetais/análise , Reprodutibilidade dos Testes , Mundo Romano , Rubia , Sensibilidade e Especificidade
7.
Mov Disord ; 20(12): 1629-33, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16078200

RESUMO

Atypical parkinsonism in Guadeloupe has been associated with the consumption of fruit and infusions or decoctions prepared from leaves of Annona muricata L. (Annonaceae), which contains annonaceous acetogenins, lipophilic inhibitors of complex I of the mitochondrial respiratory chain. We have determined the concentrations of annonacin, the major acetogenin in A. muricata, in extracts of fruit and leaves by matrix-assisted laser desorption-ionization mass spectrometry. An average fruit is estimated to contain about 15 mg of annonacin, a can of commercial nectar 36 mg, and a cup of infusion or decoction 140 microg. As an indication of its potential toxicity, an adult who consumes one fruit or can of nectar a day is estimated to ingest over 1 year the amount of annonacin that induced brain lesions in rats receiving purified annonacin by intravenous infusion.


Assuntos
Annona/química , Álcoois Graxos/efeitos adversos , Álcoois Graxos/análise , Lactonas/efeitos adversos , Lactonas/análise , Transtornos Parkinsonianos/etiologia , Acetogeninas , Annona/toxicidade , Cromatografia Líquida de Alta Pressão/métodos , Álcoois Graxos/química , Guadalupe/epidemiologia , Humanos , Lactonas/química , Peso Molecular , Extratos Vegetais/efeitos adversos , Extratos Vegetais/análise , Extratos Vegetais/química , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz/métodos
8.
Nat Prod Res ; 19(1): 75-9, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15700649

RESUMO

A new bromoindolesulfonic acid derivative, echinosulfonic acid D (1) was isolated from the New-Caledonian sponge Psammoclemma sp. in a minute quantity. The structure of the alkaloid was established by spectroscopic methods and, in particular, by ESI MSn experiments. Echinosulfonic acid D was cytotoxic to KB cells (IC50 2 microg/mL).


Assuntos
Antineoplásicos Fitogênicos/farmacologia , Alcaloides Indólicos/farmacologia , Fitoterapia , Poríferos , Ácidos Sulfônicos/farmacologia , Alcaloides/química , Alcaloides/farmacologia , Animais , Antineoplásicos Fitogênicos/química , Humanos , Alcaloides Indólicos/química , Concentração Inibidora 50 , Células KB/efeitos dos fármacos , Ácidos Sulfônicos/química
9.
J Neurochem ; 88(1): 63-9, 2004 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-14675150

RESUMO

In Guadeloupe, epidemiological data have linked atypical parkinsonism with fruit and herbal teas from plants of the Annonaceae family, particularly Annona muricata. These plants contain a class of powerful, lipophilic complex I inhibitors, the annonaceous acetogenins. To determine the neurotoxic potential of these substances, we administered annonacin, the major acetogenin of A. muricata, to rats intravenously with Azlet osmotic minipumps (3.8 and 7.6 mg per kg per day for 28 days). Annonacin inhibited complex I in brain homogenates in a concentration-dependent manner, and, when administered systemically, entered the brain parenchyma, where it was detected by matrix-associated laser desorption ionization-time of flight mass spectrometry, and decreased brain ATP levels by 44%. In the absence of evident systemic toxicity, we observed neuropathological abnormalities in the basal ganglia and brainstem nuclei. Stereological cell counts showed significant loss of dopaminergic neurones in the substantia nigra (-31.7%), and cholinergic (-37.9%) and dopamine and cyclic AMP-regulated phosphoprotein (DARPP-32)-immunoreactive GABAergic neurones (-39.3%) in the striatum, accompanied by a significant increase in the number of astrocytes (35.4%) and microglial cells (73.4%). The distribution of the lesions was similar to that in patients with atypical parkinsonism. These data are compatible with the theory that annonaceous acetogenins, such as annonacin, might be implicated in the aetiology of Guadeloupean parkinsonism and support the hypothesis that some forms of parkinsonism might be induced by environmental toxins.


Assuntos
Corpo Estriado/efeitos dos fármacos , Complexo I de Transporte de Elétrons/antagonistas & inibidores , Furanos/toxicidade , Lactonas/toxicidade , Doenças Neurodegenerativas/induzido quimicamente , Extratos Vegetais/toxicidade , Substância Negra/efeitos dos fármacos , Trifosfato de Adenosina/metabolismo , Animais , Comportamento Animal/efeitos dos fármacos , Contagem de Células , Corpo Estriado/metabolismo , Corpo Estriado/patologia , Furanos/administração & dosagem , Gliose/induzido quimicamente , Gliose/patologia , Guadalupe , Infusões Intravenosas , Lactonas/administração & dosagem , Masculino , Mitocôndrias/enzimologia , Doenças Neurodegenerativas/enzimologia , Doenças Neurodegenerativas/patologia , Neurônios/efeitos dos fármacos , Neurônios/patologia , Transtornos Parkinsonianos/etiologia , Extratos Vegetais/administração & dosagem , Ratos , Ratos Endogâmicos Lew , Substância Negra/metabolismo , Substância Negra/patologia
10.
J Nat Prod ; 66(6): 755-8, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12828457

RESUMO

Two new acetogenins, parisin (1) and salzmanolin (2), were isolated from a MeOH extract of the roots of Annona salzmanii. The structures of 1 and 2 were elucidated by spectroscopic methods including LSI-MS/MS, on both the natural compounds and their acetonide derivatives (1a and 2a). Compounds 1 and 2 showed significant activity against the KB and Vero cell lines.


Assuntos
Annona/química , Antineoplásicos Fitogênicos/isolamento & purificação , Furanos/isolamento & purificação , Plantas Medicinais/química , Animais , Antineoplásicos Fitogênicos/química , Antineoplásicos Fitogênicos/farmacologia , Brasil , Chlorocebus aethiops , Ensaios de Seleção de Medicamentos Antitumorais , Furanos/química , Furanos/farmacologia , Humanos , Células KB/efeitos dos fármacos , Estrutura Molecular , Raízes de Plantas/química , Células Tumorais Cultivadas/efeitos dos fármacos , Células Vero
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