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1.
J Ethnopharmacol ; 289: 115060, 2022 May 10.
Artigo em Inglês | MEDLINE | ID: mdl-35121049

RESUMO

ETHNOPHARMACOLOGICAL RELEVANCE: Urtica fissa E. Pritz. are important herbs and have been traditionally used as ethnic medicine to treat rheumatism, inflammation, diabetes, and benign prostatic hyperplasia by the Han, Uighur, and other minorities in China, and also as an aphrodisiac in Uighur medicine. AIMS OF THE STUDY: To determine the effect and potential mechanism of 3, 4-divanillyltetrahydrofuran (DVTF), one of the main active components isolated from U. fissa on hypogonadism in diabetic mice. MATERIALS AND METHODS: The active compound DVTF was extracted and separated from the roots of U. fissa and identified using mass spectrometry and nuclear magnetic resonance spectroscopy. A mouse model of diabetes was established using high fat and sugar diet combined with streptozotocin. In the treatment groups, mice were received different doses of DVTF for 4 weeks. Fasting blood glucose levels, physiological and biochemical indices, and the mating behavior of DM mice were analyzed. Changes in testicular morphology were assessed using light microscopy and transmission electron microscopy. The expression of testosterone synthesis-related signaling proteins was detected using western blotting. Molecular docking was used to determine the binding ability of DVTF to Nur77. RESULTS: In diabetic mice, body weight and fasting blood glucose levels decreased. Mating behavior, including mount latency, mount number, and intromission number, was improved following DVTF treatment. Plasma total testosterone, free testosterone, and insulin resistance were positively associated with the recovery of testicular pathological structures in diabetic mice. DVTF treatment increased the expression of Nur77, StAR, and P450scc in the testes of diabetic mice. DVTF and Nur77 formed chemical bonds at five sites. CONCLUSION: As one of the main active components of U. fissa, DVTF exert potential therapeutic effects on testicular injury and hypogonadism caused by diabetes through activating the expression of Nur77 and testosterone synthesis related proteins. Our result will provide new insight for the clinical application of Urtica fissa E. Pritz., especially DVTF, as a potential drug candidate in the treatment of hypogonadism in diabetes.


Assuntos
Diabetes Mellitus Experimental/tratamento farmacológico , Furanos/farmacologia , Hipogonadismo/tratamento farmacológico , Lignina/farmacologia , Urticaceae/química , Animais , Diabetes Mellitus Experimental/complicações , Feminino , Furanos/isolamento & purificação , Regulação da Expressão Gênica/efeitos dos fármacos , Hipogonadismo/etiologia , Resistência à Insulina , Lignina/isolamento & purificação , Masculino , Camundongos , Camundongos Endogâmicos ICR , Simulação de Acoplamento Molecular , Membro 1 do Grupo A da Subfamília 4 de Receptores Nucleares/genética , Comportamento Sexual Animal/efeitos dos fármacos , Disfunções Sexuais Fisiológicas/tratamento farmacológico , Disfunções Sexuais Fisiológicas/etiologia , Estreptozocina , Testículo/efeitos dos fármacos , Testosterona/sangue
2.
Nat Prod Res ; 32(3): 302-307, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28764554

RESUMO

In the present study, a new analogue of pyrrolezanthine (1) was isolated from the roots of Reynoutria ciliinervis (Nakai) Moldenke. Its structure was elucidated mainly by NMR, HR-ESI-MS and the single-crystal X-ray diffraction spectroscopic data. Meanwhile, the antimicrobial activity of compound 1 was measured, it exhibited potent antifungal activity against Sclerotinia sclerotiorum with MIC value of 31.2 µg/mL.


Assuntos
Antifúngicos/química , Antifúngicos/farmacologia , Polygonaceae/química , Pirróis/química , Anti-Infecciosos/química , Anti-Infecciosos/farmacologia , Ascomicetos/efeitos dos fármacos , Cristalografia por Raios X , Avaliação Pré-Clínica de Medicamentos/métodos , Espectroscopia de Ressonância Magnética , Testes de Sensibilidade Microbiana , Estrutura Molecular , Raízes de Plantas/química , Espectrometria de Massas por Ionização por Electrospray
3.
J Asian Nat Prod Res ; 19(12): 1245-1251, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28395521

RESUMO

A new p-hydroxybenzoic acid derivative named 4-(2'R, 4'-dihydroxybutoxy) benzoic acid (1) was isolated from the fermentation of Penicillium sp. R22 in Nerium indicum. The structure was elucidated by means of spectroscopic (HR-ESI-MS, NMR, IR, UV) and X-ray crystallographic methods. The antibacterial and antifungal activity of compound 1 was tested, and the results showed that compound 1 revealed potent antifungal activity against Colletotrichum gloeosporioides, Alternaria alternata, and Alteranria brassicae with MIC value of 31.2 µg/ml.


Assuntos
Antibacterianos/isolamento & purificação , Antifúngicos/isolamento & purificação , Benzoatos/isolamento & purificação , Nerium/microbiologia , Penicillium/química , Alternaria , Antibacterianos/química , Antibacterianos/farmacologia , Antifúngicos/química , Antifúngicos/farmacologia , Benzoatos/química , Benzoatos/farmacologia , Colletotrichum , Fermentação , Hidroxibenzoatos/química , Testes de Sensibilidade Microbiana , Estrutura Molecular
4.
Nat Prod Res ; 31(8): 951-958, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27910702

RESUMO

A new isoquinolone alkaloid named 5-hydroxy-8-methoxy-4-phenylisoquinolin-1(2H)-one (3), together with two known quinolinone alkaloids 3-O-methylviridicatin (1) and viridicatol (2) were isolated from the fermentation of an endophytic fungus Penicillium sp. R22 in Nerium indicum. Their structures were elucidated by NMR, IR and MS data, and were also confirmed by comparing with the reported data in the literature. Meanwhile, the antibacterial and antifungal activities of all compounds were tested, and the results showed that three compounds had strong antifungal activity. Among them, compound 2 revealed potent antibacterial activity against Staphylococcus aureus with MIC value of 15.6 µg/mL.


Assuntos
Alcaloides/química , Antibacterianos/farmacologia , Antifúngicos/farmacologia , Isoquinolinas/isolamento & purificação , Nerium/microbiologia , Penicillium/química , Alcaloides/isolamento & purificação , Alcaloides/farmacologia , Antibacterianos/química , Antifúngicos/química , Avaliação Pré-Clínica de Medicamentos/métodos , Endófitos/química , Hidroxiquinolinas/química , Hidroxiquinolinas/isolamento & purificação , Isoquinolinas/química , Isoquinolinas/farmacologia , Testes de Sensibilidade Microbiana , Estrutura Molecular , Penicillium/fisiologia , Quinolonas/química , Quinolonas/isolamento & purificação , Staphylococcus aureus/efeitos dos fármacos
5.
Zhong Yao Cai ; 38(10): 2098-101, 2015 Oct.
Artigo em Chinês | MEDLINE | ID: mdl-27254923

RESUMO

OBJECTIVE: To investigate the chemical constituents from the stems and branches of Sorbaria arborea. METHODS: The chemical constituents were isolated and purified by silica gel column chromatography, Sephadex LH-20 column chromatography and recrystallization. Their structures were identified by physicochemical properties and spectra analysis. RESULTS: Ten compounds were isolated and identified as ursolic acid (1), cucurbitacin F (2), (-) -epicatechin (3), daucosterol (4), arbutin (5), 3-O-ß-anthemisol (6), 2,6-dimethoxy-p-hydroquinone-4-O-ß-D-glucopyranoside (7), lupeol (8), betulin (9) and lup-20 (29) -en-3ß, 30-diol (10). CONCLUSION: All the compounds are isolated from this plant for the first time, and compounds 1, 6 - 8 and 10 are obtained from Sorbaria genus for the first time.


Assuntos
Cromatografia , Medicamentos de Ervas Chinesas/química , Compostos Fitoquímicos/análise , Caules de Planta/química , Rosaceae/química , Arbutina/isolamento & purificação , Catequina/isolamento & purificação , Triterpenos Pentacíclicos/isolamento & purificação , Compostos Fitoquímicos/isolamento & purificação , Plantas Medicinais/química , Sitosteroides/isolamento & purificação , Triterpenos/isolamento & purificação , Ácido Ursólico
6.
Environ Toxicol Pharmacol ; 37(3): 1015-27, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24751684

RESUMO

The oxidative status and morphological changes of mouse liver exposed to cadmium chloride (Cd(II)) and therapeutic potential of blueberry (Vaccinium corymbosum L.) extract against Cd(II)-induced hepatic injury were investigated. A variety of parameters were evaluated, including lipid peroxidation (LPO), protein carbonyl (PCO) level, DNA fragment, as well as antioxidative defense system (i.e., superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH)). Elemental analysis and evaluation of morphological changes and NO levels were also performed. Exposure to Cd(II) led to increased LPO and PCO as well as DNA fragment and a reduction of SOD and CAT activities, however, the content of GSH elevated probably due to biological adaptive-response. In contrast, co-treatment of anthocyanin (Ay) inhibited the increased oxidative parameters as well as restored the activities of antioxidative defense system in a dose-dependent manner. Ay administration regained these morphological changes caused by intoxication of Cd(II) to nearly normal levels. Moreover, the accumulation of Cd(II) in liver may be one of the reasons for Cd(II) toxicity and Ay can chelate with Cd(II) to reduce Cd(II) burden. The influence of Cd(II) on the Zn and Ca levels can also be adjusted by the co-administration of Ay. Exposure to Cd(II) led to an increase of NO and Ay reduced NO contents probably by directly scavenging. Potential mechanisms for the protective effect of Ay have been proposed, including its anti-oxidative and anti-inflammatory effect along with the metal-chelating capacity. These results suggest that blueberry extract may be valuable as a therapeutic agent in combating Cd(II)-induced tissue injury.


Assuntos
Antocianinas/uso terapêutico , Anti-Inflamatórios/uso terapêutico , Antioxidantes/uso terapêutico , Quelantes/uso terapêutico , Doença Hepática Induzida por Substâncias e Drogas/tratamento farmacológico , Vaccinium , Alanina Transaminase/sangue , Animais , Antocianinas/farmacologia , Anti-Inflamatórios/farmacologia , Antioxidantes/farmacologia , Aspartato Aminotransferases/sangue , Cádmio/toxicidade , Catalase/metabolismo , Quelantes/farmacologia , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Doença Hepática Induzida por Substâncias e Drogas/metabolismo , Doença Hepática Induzida por Substâncias e Drogas/patologia , Fragmentação do DNA/efeitos dos fármacos , Glutationa/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/efeitos dos fármacos , Fígado/metabolismo , Fígado/patologia , Masculino , Camundongos , Fitoterapia , Extratos Vegetais/farmacologia , Extratos Vegetais/uso terapêutico , Carbonilação Proteica/efeitos dos fármacos , Superóxido Dismutase/metabolismo
7.
Zhongguo Zhong Yao Za Zhi ; 31(14): 1166-8, 2006 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-17048586

RESUMO

OBJECTIVE: To investigate the constituents of Ervatamia hainanensis systematically. METHOD: Various chromatographic techniques were applied to isolate and purify the constituents of this plant. The structures were elucidated by spectroscopic analysis. RESULT: Eight compounds were obtained, which were identified as alpha-amyrin acetate (1), 11-oxo-alpha-amyrin acetate (2), beta-sitosterol (3), cycloart-23-ene-3beta, 25-diol(4), cycloart-25-ene-3beta, 24-diol (5), 5alpha, 8alpha-epidioxyergosta-6, 22-dien-3beta-ol (6), ibogamin-3-one (7), beta-daucosterol (8). CONCLUSION: Compounds 1, 2, 4- 7 were isolated from this plant for the first time.


Assuntos
Apocynaceae/química , Ergosterol/análogos & derivados , Ácido Oleanólico/análogos & derivados , Plantas Medicinais/química , Triterpenos/isolamento & purificação , Ergosterol/química , Ergosterol/isolamento & purificação , Ácido Oleanólico/química , Ácido Oleanólico/isolamento & purificação , Raízes de Plantas/química , Caules de Planta/química , Triterpenos/química
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