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1.
Klin Monbl Augenheilkd ; 239(7): 923-928, 2022 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-34911122

RESUMO

BACKGROUND/AIM: To describe demographic and clinical characteristics, treatment, and visual prognosis of Coats disease in Hispanic patients. METHODS: A retrospective chart review was performed on nine patients (ten eyes) diagnosed with Coats disease in our two clinical centrers from 2004 - 2017. RESULTS: Mean age at diagnosis was 5.5 years (range 1 - 12 years) and mean follow-up time was 48 months (range 9 - 108 months). Eight patients (89%) were male and had unilateral disease and one (11%) female patient had bilateral disease. In 40% of the cases, patients were asymptomatic. Visual acuity at first presentation was worse than hand motion in 60% of the eyes. Half of the eyes (5/10 eyes, 50%) had exudative retinal detachment (≥ stage IIIA). Vascular ablation with cryotherapy combined with retinal photocoagulation was the most frequent therapeutic approach (40%). Despite anatomical success at 6 months in 100% of the treated eyes, visual outcome at 1 year of treatment was poor (worse than 20/200) in 70% of the cases. CONCLUSIONS: In our case series, patients were mostly asymptomatic on presentation, with severe stages of Coats disease. Even with anatomical success after surgical treatment in all treated cases, long-term visual prognosis remained very limited.


Assuntos
Descolamento Retiniano , Telangiectasia Retiniana , Feminino , Seguimentos , Hispânico ou Latino , Humanos , Lactente , Fotocoagulação a Laser , Masculino , Descolamento Retiniano/diagnóstico , Descolamento Retiniano/cirurgia , Telangiectasia Retiniana/diagnóstico , Telangiectasia Retiniana/terapia , Estudos Retrospectivos
2.
Bol. latinoam. Caribe plantas med. aromát ; 15(1): 53-60, ene. 2016. tab
Artigo em Inglês | LILACS | ID: biblio-907517

RESUMO

Essential oils obtained from new plant species with metabolomes unexplored or poorly known are a natural resource to find molecules with deterrent (irritant) effect. The aim of this study was to evaluate the chemical composition and the termite repellent activity of the essential oils from Ageratina jocotepecana. The repellent effect was determined by the pine drywood termite Incisitermes marginipennis behavior of to sense the contact of the tunnel wall in the wooden colony in the presence of an irritant obstacle caused by essential oils. Gas chromatographic analysis of the essential oils from flower, leaf, and stem showed quantitative and qualitative differences in components. Twenty-eight volatile components were identified by their mass spectra (MS). beta-caryophyllene, carvacrol, spathulenol, and terpinen-4-ol were the four major components, of them in relation 0.1 M citronellol, the 0.1 M carvacrol was the best repellent of the termite. Essential oils from A. jocotepecana exhibited a termite repellent effect due to their major components. Additionally, more research about the termite repellent action of carvacrol is still needed.


Los aceites esenciales obtenidos de nuevas especies de plantas con metabolomas inexplorados o poco conocidos son un recurso natural para encontrar moléculas con efecto disuasivo (irritante). El propósito del estudio fue evaluar la composición química de los aceites esenciales de Ageratina jocotepecana y su actividad repelente de termitas. El efecto repelente fue determinado por el comportamiento de las termitas de la madera seca de pino Incisitermes marginipennis de sentir el contacto de la pared del túnel en la colonia de madera en la presencia de un obstáculo irritante causado por los aceites esenciales. El análisis de cromatografía de gases de los aceites esenciales de flores, hojas y tallo mostró diferencias cuantitativas y cualitativas en componentes. Veintiocho componentes volátiles fueron identificados por sus espectros de masas (MS). beta-cariofileno, carvacrol, spathulenol y terpinen-4-ol fueron los cuatro componentes mayoritarios, de ellos en relación con 0,1 M citronelol el control positivo, el carvacrol 0,1 M fue el mejor repelente de la termita. Además, más investigación sobre la acción repelente de termitas de carvacrol se necesita realizar.


Assuntos
Ageratina/química , Isópteros , Repelentes de Insetos/farmacologia , Óleos Voláteis/química , Óleos Voláteis/farmacologia , Extratos Vegetais/farmacologia , Cromatografia Gasosa , Repelentes de Insetos/química , Extratos Vegetais/química , Terpenos/isolamento & purificação
3.
J Nat Prod ; 77(4): 1005-12, 2014 Apr 25.
Artigo em Inglês | MEDLINE | ID: mdl-24702233

RESUMO

Chemical investigation of the hexanes extracts of Ageratina jocotepecana afforded (-)-(5S,9S,10S,13S)-labd-7-en-15-oic acid (1), methyl (-)-(5S,9S,10S,13S)-labd-7-en-15-oate (2), (+)-(5S,8R,9R,10S,13R)-8-hydroxylabdan-15-oic acid (3), and (-)-(5S,9S,10S,13Z)-labda-7,13-dien-15-oic acid (5). The coexistence of (13R)- and (13S)-labdanes in this member of the Asteraceae family was demonstrated by vibration circular dichroism measurements of ester 2 and methyl (+)-(5S,8R,9R,10S,13R)-8-hydroxylabdan-15-oate (4) in comparison to the DFT B3LYP/DGDZVP-calculated spectra. In addition, transformation of 1 and 3 with HClO4 in MeOH yielded epimeric methyl (+)-(5S,10S,13S)-labd-8-en-15-oate (6) and methyl (+)-(5S,10S,13R)-labd-8-en-15-oate (7), respectively, confirming the presence of C-13 epimers in this plant. Diterpene 1 showed remarkable antibacterial activity against Bacillus subtilis (MIC 0.15 mg/mL) and Staphylococcus aureus (MIC 0.78 mg/mL), while diterpene 3 exhibited moderate activities against the same organisms.


Assuntos
Ageratina/química , Antibacterianos/química , Antibacterianos/isolamento & purificação , Diterpenos/química , Diterpenos/isolamento & purificação , Antibacterianos/farmacologia , Bacillus subtilis/efeitos dos fármacos , Dicroísmo Circular , Diterpenos/farmacologia , México , Testes de Sensibilidade Microbiana , Modelos Moleculares , Estrutura Molecular , Staphylococcus aureus/efeitos dos fármacos , Estereoisomerismo
4.
Z Naturforsch C J Biosci ; 63(11-12): 922-4, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-19227847

RESUMO

D-(+)-Pinitol, a natural product of the group of cyclitols, was purified for the first time from an aqueous extract of the heartwood of Enterolobium cyclocarpum, and its chemical structure was determined.


Assuntos
Fabaceae/química , Inositol/análogos & derivados , Brasil , Óxido de Deutério , Ecossistema , Inositol/química , Inositol/isolamento & purificação , Espectroscopia de Ressonância Magnética , México , Árvores
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