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Medicinas Complementares
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1.
Medicine (Baltimore) ; 99(45): e23077, 2020 Nov 06.
Artigo em Inglês | MEDLINE | ID: mdl-33157973

RESUMO

BACKGROUND: Warm needling acupuncture (WNA) has been widely utilized for pain management in patients with diabetic peripheral neuropathy (DPN). However, its results are still inconsistent, and no systematic review has specifically addressed this issue. Thus, this systematic review will comprehensively and systematically investigate the effectiveness and safety of WNA for pain relief in DPN. METHODS: A comprehensive literature search of MEDLINE, EMBASE, Cochrane Library, Web of Science, Scopus, Allied and Complementary Medicine Database, CBM database, and China National Knowledge Infrastructure will be performed for randomized controlled trials that report WNA for pain relief in patients with DPN. All electronic databases will be searched from initial to the present without limitations of language and publication status. Two investigators will independently screen papers, collect data, and assess study quality. Cochrane risk of bias tool will be used for study quality assessment, and evidence quality will be evaluated using Grading of Recommendations Assessment, Development and Evaluations approach. RevMan 5.3 software will be applied for running statistical analysis. RESULTS: This study will summarize the evidence for the effectiveness and safety of WNA for the management of pain in patients with DPN. CONCLUSIONS: The findings of this study may provide helpful evidence to judge whether WNA for pain relief in DPN is effective or not.


Assuntos
Terapia por Acupuntura/métodos , Neuropatias Diabéticas/terapia , Neuralgia/terapia , Projetos de Pesquisa , Revisões Sistemáticas como Assunto , Temperatura Alta , Humanos , Agulhas , Ensaios Clínicos Controlados Aleatórios como Assunto , Resultado do Tratamento
2.
J Asian Nat Prod Res ; 15(11): 1210-3, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23822190

RESUMO

A new naphtho[1,2-b]furan, 2,9-dihydroxy-7-methoxy-4-methylnaphtha[1,2-b]furan-3(2H)-one (1), along with 10 known compounds vanillic acid (2), naringenin (3), glyceryl-1-tetracosanoate (4), moracin J (5), 1,3,8-trihydroxyanthraquinone (6), esculetin (7), mauritianin (8), kaempferol 3-neohesperidoside (9), ß-sitosterol (10), and ß-daucosterol (11), was isolated from the leaves of Cassia fistula. The structure of the new compound was determined by NMR and X-ray analysis. Compounds 1, 3, 5-9 were isolated from this plant for the first time. The naphtha[1,2-b]furan was firstly isolated from the natural resources.


Assuntos
Cassia/química , Medicamentos de Ervas Chinesas/isolamento & purificação , Furanos/isolamento & purificação , Naftalenos/isolamento & purificação , Medicamentos de Ervas Chinesas/química , Furanos/química , Quempferóis/química , Quempferóis/isolamento & purificação , Estrutura Molecular , Naftalenos/química , Ressonância Magnética Nuclear Biomolecular , Folhas de Planta/química , Sitosteroides/química , Sitosteroides/isolamento & purificação
3.
Zhongguo Zhong Yao Za Zhi ; 38(7): 1014-7, 2013 Apr.
Artigo em Chinês | MEDLINE | ID: mdl-23847948

RESUMO

Fifteen compounds were obtained from the twigs and leaves of Caesalpinia minax. Their structures were identified as apigenin (1), 5,7,3',4'- tetrahydroxy-3-methoxyflavone (2), luteolin-5, 3 '-dimethyl-ether (3), thevetiaflavon (4), apigenin-7-O-beta-D-glucuronide (5), bonducellin (6), 7-hydroxy-3-( 4-hydroxybenzylidene )-chroman-4-one (7), 3-deoxysappanchalcone (8), 5-acetonyl-7-hydroxy-2-methyl chromone (9), 4-(trans)-acetyl-3,6,8-trihydroxy-3-methyl-dihydronaphthalenone (10), 4-(cis)-acetyl-3,6,8-trihydroxy-3-methyl-dihydronaphthalenone (11), vanillic acid (12), omega-hydroxypropioquaiacone (13), syringaresinol (14) and uracil (15). All compounds were isolated from C. minax for the first time. Compounds 1-14 were phenolic compounds and compounds 1-5, 9-13 and 15 were isolated from the genus Caesalpinia for the first time.


Assuntos
Caesalpinia/química , Medicamentos de Ervas Chinesas/química , Fenóis/química , Estrutura Molecular , Folhas de Planta/química
4.
Planta Med ; 77(16): 1841-4, 2011 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21674439

RESUMO

Five new 1,3-diarylpropan-1-ols, combretol A-E (1- 5), together with one known coumarin (6) and ten known triterpenes (7-16), were isolated from Combretum yunnanense. Their structures were determined by spectroscopic investigation, including ¹H and ¹³C NMR, NOESY, HSQC, HMBC, and HRESIMS analyses. This is the first report on the occurrence of 1,3-diarylpropan-1-ols and coumarin in the Combretum genus including C. yunnanense. Also, to the best of our knowledge, 1,3-diarylpropan-1-ols are rare in nature.


Assuntos
Combretum/química , Cumarínicos/isolamento & purificação , Medicamentos de Ervas Chinesas/isolamento & purificação , Triterpenos/isolamento & purificação , China , Cumarínicos/química , Medicamentos de Ervas Chinesas/química , Espectroscopia de Ressonância Magnética , Medicina Tradicional Chinesa , Estrutura Molecular , Componentes Aéreos da Planta/química , Triterpenos/química
5.
Planta Med ; 77(5): 481-4, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21053158

RESUMO

New chalcone and dimeric chalcones with 1,4- P-benzoquinone residue, combrequinone A (1), combrequinone B (2), and combrequinone C (3), along with three known compounds (4-6), were isolated from the ethanolic extract of the stems and leaves of Combretum yunnanense, and their structures were determined by spectroscopic analysis. Compounds 1-3 were evaluated for in vitro cytotoxicity against five human cancer cell lines: HL-60, SMMC-7721, A-549, MCF-7, and SW480. Compounds 1, 2 and 3 were found to be most potent against HL-60 acute leukemia cells, with IC50 values of 4.63, 4.07, and 1.26 µM, respectively.


Assuntos
Sobrevivência Celular/efeitos dos fármacos , Chalconas/farmacologia , Gleiquênias/química , Extratos Vegetais/farmacologia , Benzoquinonas/química , Linhagem Celular Tumoral , Chalconas/química , Humanos , Concentração Inibidora 50 , Espectroscopia de Ressonância Magnética , Extratos Vegetais/química , Folhas de Planta/química , Caules de Planta/química
6.
Phytochemistry ; 71(5-6): 641-7, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20100622

RESUMO

Kaempferol glycosides, named palmatosides A (1), B (2) and C (3), together with three known kaempferol glycosides, multiflorins A (4) and B (5), and afzelin (6), were isolated from the roots of the fern Neocheiropteris palmatopedata. Palmatosides A (1) and B (2) each possessed an unusual sugar moiety containing a 4,4-dimethyl-3-oxo-butoxy substituent group. The isolated compounds were evaluated for their cancer chemopreventive potential based on their ability to inhibit tumor necrosis factor alpha (TNF-alpha)-induced NF-kappaB activity, nitric oxide (NO) production, aromatase, quinone reductase 2 (QR2) and COX-1/-2 activities. Palmatosides B (2) and C (3) inhibited TNF-alpha-induced NF-kappaB activity with IC(50) values of 15.7 and 24.1 microM, respectively; multiflorin A (4) inhibited aromatase enzyme with an IC(50) value of 15.5 microM; afzelin (6) showed 68.3% inhibition against QR2 at a concentration of 11.5 microg/ml; palmatoside A (1) showed 52% inhibition against COX-1 enzyme at a concentration of 10 microg/ml; and multiflorin B (5) showed 52% inhibition against nitric oxide production at a concentration of 20 microg/ml. In addition, compounds 3-6 were shown to bind QR2 enzyme using LC-MS ultrafiltration binding assay.


Assuntos
Antineoplásicos Fitogênicos/farmacologia , Inibidores da Aromatase/farmacologia , Inibidores de Ciclo-Oxigenase/farmacologia , Glicosídeos/farmacologia , Extratos Vegetais/farmacologia , Polypodiaceae/química , Antineoplásicos Fitogênicos/isolamento & purificação , Inibidores da Aromatase/isolamento & purificação , Linhagem Celular , Linhagem Celular Tumoral , Inibidores de Ciclo-Oxigenase/isolamento & purificação , Glicosídeos/isolamento & purificação , Humanos , Concentração Inibidora 50 , Quempferóis/química , Quempferóis/isolamento & purificação , Quempferóis/farmacologia , NAD(P)H Desidrogenase (Quinona)/antagonistas & inibidores , NF-kappa B/antagonistas & inibidores , Óxido Nítrico/antagonistas & inibidores , Extratos Vegetais/química , Raízes de Plantas , Fator de Necrose Tumoral alfa/antagonistas & inibidores
7.
Shi Yan Sheng Wu Xue Bao ; 35(4): 324-8, 2002 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-15346992

RESUMO

In this study, two hundred and forty bacterial strains were isolated from inner tissue of potato tubers collected from DaTong, TaiYuan and Inner Mongolia Autonomous regions. On the basis of antagonistic examination in vitro, fifty and five bacteria strains were characterized for antagonistic bacteria to ring rot of potato. It was 22.9 percentage of all bacteria strains. The biggest radius of suppression circle was 13 mm. Nine strains were chosen for their suppression of bacterial ring rot, blackleg and dry rot of potato. These strains were bacteriologically ideatified. Strain 118 was Pseudomonas fluorescens biovar V. Strain 110 was Bacillus pumilus. Strain 085 was Bacillus stearothermophilus. Strain 069 was Erwinia herbicola. Strain 043 was Xanthomomas fragariae. Strain 116 was Curtobacterium. Strains A-10' and T3 were Bacillus. Strain H1-6 was Pseudomonas fluorescens.


Assuntos
Bactérias/isolamento & purificação , Erwinia/fisiologia , Doenças das Plantas/microbiologia , Solanum tuberosum/microbiologia , Bacillus/isolamento & purificação , Bacillus/fisiologia , Erwinia/isolamento & purificação , Controle Biológico de Vetores/métodos , Doenças das Plantas/prevenção & controle , Pseudomonas fluorescens/isolamento & purificação , Pseudomonas fluorescens/fisiologia , Xanthomonas/isolamento & purificação , Xanthomonas/fisiologia
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