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1.
Nat Prod Res ; 36(16): 4153-4158, 2022 Aug.
Article in English | MEDLINE | ID: mdl-34498969

ABSTRACT

Cholinesterase (ChE) inhibitors are currently the main drugs used to treat the cognitive symptoms of Alzheimer's disease (AD). Dual cholinesterase inhibitors, that is, compounds capable of inhibiting both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), are considered a new potential approach for the long-term treatment of patients with AD. We evaluated the ethyl acetate extract of Phomopsis sp., grown in liquid medium malt extract and potato dextrose (PDB), an endophyte isolated from the Brazilian medicinal plant Hancornia speciosa. The anticholinesterase (AChE) and butyrylcholinesterase (BuChE) activities were evaluated. The extracts exhibited dual action against AChE and BuChE. The compounds isolated from these extracts, nectriapyrone (1) and tryptophol (2), showed inhibitory action on BuChE (IC50 = 29.05 and 34.15 µM respectively), being selective towards BuChE. The discovery of selective BuChE inhibitors is extremely important for the development of drugs that can be used in the treatment of patients diagnosed with AD.


Subject(s)
Acetylcholinesterase , Alzheimer Disease , Alcohols , Alzheimer Disease/drug therapy , Butyrylcholinesterase , Cholinesterase Inhibitors/pharmacology , Humans , Indoles , Phomopsis
2.
J Nat Med ; 66(3): 428-34, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22146971

ABSTRACT

Lippia gracilis Schauer is an aromatic plant widely found in Northeastern Brazil. The leaf infusions or decoctions and alcoholic macerate are used for some inflammatory diseases and headache. This paper reports the isolation of naringenin by semi-preparative liquid chromatography from the methanolic extract of L. gracilis (ELg) and the evaluation of the analgesic and anti-inflammatory activities of this extract by measuring nociception through acetic acid, formalin, and hot-plate tests in carrageenan-induced inflammation in mice. Following oral administration, ELg (100, 200, and 400 mg/kg) significantly reduced the number of writhes in the writhing test and the time of paw licks in both phases of the formalin test when compared to the control group animals. Mice treated with ELg did not exhibit any behavioral alteration during the hot plate and rota-rod tests, suggesting non-participation of the supraspinal components in the modulation of pain by ELg and no motor abnormality. The oral administration of 400 mg/kg of ELg produced an anti-inflammatory effect on peritonitis induced by carrageenan. These effects can be associated with a decrease of inflammatory mediator synthesis by compounds of ELg, such as naringenin, which has anti-inflammatory action as already described.


Subject(s)
Analgesics/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Lippia/chemistry , Pain/drug therapy , Plant Extracts/therapeutic use , Analgesics/chemistry , Animals , Anti-Inflammatory Agents/chemistry , Brazil , Male , Mice , Plant Extracts/chemistry
3.
Rev. bras. farmacogn ; 21(3): 402-406, maio-jun. 2011. ilus, graf, tab
Article in English | LILACS | ID: lil-593300

ABSTRACT

Myrcia uniflora Barb. Rodr., Myrtaceae, popularly known as "pedra-hume-caá" in Brazil, is sold as dry extracts in capsules or as tinctures for the treatment of diabetes mellitus. Previous phytochemical studies on this species described the occurrence of the flavonoids mearnsitrin and myricitrin. In the present study, the chromatographic profiles of M. uniflora leaves and commercial extracts were determined using HPLC-PAD. Myricitrin was used as an external standard in the development and validation of the HPLC method. The proposed method is simple, rapid and reliable and can be successfully applied in industry for standardization of herbs and phytomedicines commercialised in Brazil as "pedra-hume-caá".

4.
Biomed Chromatogr ; 23(6): 573-80, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19277954

ABSTRACT

Phyllanthus niruri L., commonly known in Brazil as 'quebra-pedra', has long been used in the treatment of diverse diseases and especially urolithiasis. The therapeutic effects of P. niruri are attributed to various compounds present in the plant, including the hydrolysable tannin corilagin. In the present study, high-performance liquid chromatography (HPLC-/PAD) profiles of leaves and commercial extracts of P. niruri were examined and three compounds, found to be present in all of the samples studied, were isolated by open column chromatography over C18)silica gel followed by preparative HPLC. These compounds were identified by nuclear magnetic resonance as corilagin, rutin and ethyl 3,4,5-trihydroxybenzoate. Corilagin, which has been proposed as a phytochemical marker for P. niruri, was employed as an external standard in the development and validation of a rapid and efficient qualitative and quantitative HPLC assay for the analyte. The method may be applied in the standardization of herbs and phytomedicines commercialized in Brazil as quebra-pedra.


Subject(s)
Chromatography, High Pressure Liquid/methods , Gallic Acid/analogs & derivatives , Glucosides/analysis , Phyllanthus/chemistry , Plant Extracts/analysis , Rutin/analysis , Chromatography, High Pressure Liquid/economics , Chromatography, High Pressure Liquid/instrumentation , Gallic Acid/analysis , Gallic Acid/isolation & purification , Hydrolyzable Tannins , Magnetic Resonance Spectroscopy , Plant Leaves/chemistry , Reproducibility of Results , Rutin/isolation & purification , Sensitivity and Specificity , Time Factors
5.
Z Naturforsch C J Biosci ; 64(11-12): 824-30, 2009.
Article in English | MEDLINE | ID: mdl-20158153

ABSTRACT

In the course of our continuous search for bioactive metabolites from endophytic fungi living in plants from the Brazilian flora, leaves of Alibertia macrophylla (Rubiaceae) were submitted to isolation of endophytes, and two species of Penicillium were isolated. The acetonitrile fraction obtained in corn from a culture of Penicillium sp. 1 afforded orcinol (1). On the other hand, Penicillium sp. 1 cultivated in potato-dextrose-broth furnished two different compounds, cyclo-(L-Pro-L-Val) (2) and uracil (3). The chromatographic fractionation of the acetonitrile fraction obtained from Penicillium sp. 2 led to three dihydroisocoumarins, 4-hydroxymellein (4), 8-methoxymellein (5) and 5-hydroxymellein (6). Compounds 5 and 6 were obtained from the Penicillium genus for the first time. Additionally, metabolites 1-6 were evaluated for their antifungal and acetylcholinesterase (AChE) inhibitory activities. The most active compounds 1 and 4 exhibited detection limits of 5.00 and 10.0 microg against Cladosporium cladosporioides and C. sphaerospermum, respectively. Compound 2 showed a detection limit of 10.0 microg, displaying potent AChE inhibitory activity.


Subject(s)
Penicillium/chemistry , Penicillium/metabolism , Rubiaceae/chemistry , Antifungal Agents/isolation & purification , Antifungal Agents/pharmacology , Brazil , Cholinesterase Inhibitors/isolation & purification , Cholinesterase Inhibitors/pharmacology , Magnetic Resonance Spectroscopy/methods , Models, Molecular , Ochratoxins/chemistry , Ochratoxins/isolation & purification , Penicillium/drug effects , Penicillium/isolation & purification , Rubiaceae/microbiology , Solanum tuberosum/microbiology , Spectrophotometry , Zea mays/microbiology
6.
An Acad Bras Cienc ; 80(3): 427-32, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18797795

ABSTRACT

To find out natural antimicrobial agents as alternative in therapeutics and to preserve food, the methanol extract of Solanum palinacanthum aerial parts was submitted to purification steps guided by antibacterial and antifungal assays. As a consequence, the flavonoid rutin and 3,5-dicaffeoylquinic acid were isolated by column chromatography and high performance liquid chromatography, and identified by mass and nuclear magnetic resonance spectrometry. Minimal inhibitory concentrations (MIC) of the quinic acid derivative against Aeromonas hydrophila, Bacillus subtilis, Staphylococcus aureus and the fungus Aspergillus ochraceus were 250, 1000, 1000 and > 568 microg/mL, respectively. Against the same microorganisms, MIC for rutin were 1000, > 1000, > 1000 and 35 microg/mL, respectively. Rutin was very promising for A. ochraceus control, since its MIC against such fungus was close to the one observed for benzalkonium chloride, which is used as a fungicide in Brazil.


Subject(s)
Anti-Bacterial Agents/isolation & purification , Antifungal Agents/isolation & purification , Solanum/chemistry , Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Aspergillus ochraceus/drug effects , Chromatography , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Magnetic Resonance Spectroscopy , Mass Spectrometry , Microbial Sensitivity Tests , Plant Extracts/pharmacology
7.
An. acad. bras. ciênc ; 80(3): 427-432, Sept. 2008. ilus, tab
Article in English | LILACS | ID: lil-491823

ABSTRACT

To find out natural antimicrobial agents as alternative in therapeutics and to preserve food, the methanol extract of Solanum palinacanthum aerial parts was submitted to purification steps guided by antibacterial and antifungal assays. As a consequence, the flavonoid rutin and 3,5-dicaffeoylquinic acid were isolated by column chromatographyand high performance liquid chromatography, and identified by mass and nuclear magnetic resonance spectrometry. Minimal inhibitory concentrations (MIC) of the quinic acid derivative against Aeromonas hydrophila, Bacillus subtilis, Staphylococcus aureus and the fungus Aspergillus ochraceus were 250, 1000, 1000 and > 568µg/mL, respectively. Against the same microorganisms, MIC for rutin were 1000, > 1000, > 1000 and 35µg/mL, respectively. Rutinwas very promising for A. ochraceus control, since its MIC against such fungus was close to the one observed for benzalkonium chloride, which is used as a fungicide in Brazil.


Com vistas a descobrir antimicrobianos de origem natural para uso terapêutico ou para a preservação de alimentos, o extrato metanólico das partes aéreas de Solanum palinacanthum foi submetido a fracionamentos direcionados por testes para avaliar a atividade antibacteriana e antifúngica. Em decorrência, o flavonóide rutina e o ácido 3,5-dicafeoilquínico foram isolados por cromatografia em coluna e por cromatografia líquida de alta eficiência, para serem identificados por espectrometria de massas e de ressonância magnética nuclear. As concentrações inibitórias mínimas (CIM) do derivado do ácido cafeico contra Aeromonas hydrophila, Bacillus subtilis, Staphylococcus aureus e o fungo Aspergillus ochraceus foram 250, 1000, 1000 e > 568µg/mL, respectivamente. Contra os mesmos organismos, os valores de CIM para a rutina foram 1000, > 1000, > 1000 e 35µg/mL, respectivamente. A rutina mostrou-se muito promissora para o controle de A. ochraceus, pois seu valor de CIM contra tal fungo foi bem próximo ao observado para o cloreto de benzalcônio, que é empregado como fungicida no Brasil.


Subject(s)
Anti-Bacterial Agents/isolation & purification , Antifungal Agents/isolation & purification , Solanum/chemistry , Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Aspergillus ochraceus/drug effects , Chromatography , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Magnetic Resonance Spectroscopy , Mass Spectrometry , Microbial Sensitivity Tests , Plant Extracts/pharmacology
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