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1.
Am J Chin Med ; 45(1): 159-172, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28081628

RESUMEN

Schisandra chinensis (SC) and its main constituent, schizandrin (SCH) exhibit anti-inflammatory and anti-allergic activities. Allergic and inflammatory reactions are aggravated via caspase-1 signaling pathway. However, the regulatory effects of SC and SCH on caspase-1 activation have not been clarified yet. In this study, we aimed to clarify the anti-allergic effects of SC and SCH using an ovalbumin (OVA)-sensitized mice and anti-CD3 and anti-CD28 antibodies-stimulated splenocytes. SC or SCH significantly inhibited the levels of immunoglobulin (Ig)E, IgG1, or interleukin (IL)-4 in serum of OVA-sensitized mice. SC or SCH significantly inhibited the levels of IL-6, tumor necrosis factor (TNF)-[Formula: see text], and IL-1[Formula: see text] in spleen of the OVA-sensitized mice. SC or SCH significantly suppressed the expression of caspase-1 and receptor-interacting protein (RIP)-2 in spleen of the OVA-sensitized mice. In activated splenocytes, SC or SCH significantly decreased the expression of caspase-1 and RIP-2 as well as the production of IL-6 and TNF-[Formula: see text]. We suggest that SC and SCH exert an anti-allergic effect by down-regulating caspase-1 signaling.


Asunto(s)
Caspasa 1/efectos de los fármacos , Ciclooctanos/farmacología , Hipersensibilidad/inmunología , Lignanos/farmacología , Extractos Vegetales/farmacología , Compuestos Policíclicos/farmacología , Schisandra , Bazo/efectos de los fármacos , Animales , Caspasa 1/metabolismo , Regulación hacia Abajo , Inmunoglobulina E/efectos de los fármacos , Inmunoglobulina E/inmunología , Inmunoglobulina G/efectos de los fármacos , Inmunoglobulina G/inmunología , Interleucina-1beta/efectos de los fármacos , Interleucina-1beta/inmunología , Interleucina-4/inmunología , Interleucina-6/inmunología , Ratones , Ovalbúmina , Proteína Serina-Treonina Quinasa 2 de Interacción con Receptor , Proteína Serina-Treonina Quinasas de Interacción con Receptores/efectos de los fármacos , Proteína Serina-Treonina Quinasas de Interacción con Receptores/metabolismo , Bazo/citología , Factor de Necrosis Tumoral alfa/efectos de los fármacos , Factor de Necrosis Tumoral alfa/inmunología
2.
BMJ Open ; 6(4): e008583, 2016 Apr 06.
Artículo en Inglés | MEDLINE | ID: mdl-27053265

RESUMEN

OBJECTIVES: Although there has been considerable discussion about the social safety net, few studies related to effect of duration of continuous receipt of Medical Aid on healthcare utilisation have been conducted. Therefore, we investigate whether the duration of receiving Medical Aid affected medical care utilisation. SETTING: Data were collected from the Korean Welfare Panel Study conducted from 2008 to 2012. PARTICIPANTS: We included 11,783 samples. INTERVENTIONS: Estimating changes in their healthcare utilisation during specific time intervals (1, 2 and ≥3 years) after they switched from National Health Insurance to Medical Aid. PRIMARY AND SECONDARY OUTCOME MEASURES: Number of outpatient visits. RESULTS: The number of outpatient visits per year was 0.0.051-fold higher (p value: 0.434) among those who were Medical Aid beneficiaries for a continuous period of 1 year, 0.0.267-fold higher (p value: 0.000) among those who were beneficiaries for a continuous period of 2 years, and 0.0.562-fold higher (p value:<0.0001) among those who were beneficiaries for a continuous period of 3 years than it was among those who were beneficiaries of National Health Insurance. CONCLUSIONS: Our results reflect an association between the number of consecutive years of receiving Medical Aid and number of outpatient visits. Since duration of dependence is correlated with reduced exit rates, limits on length of benefits should be considered to strengthen the incentive to return to work.


Asunto(s)
Atención Ambulatoria/estadística & datos numéricos , Atención Ambulatoria/tendencias , Aceptación de la Atención de Salud/estadística & datos numéricos , Adulto , Estudios Transversales , Femenino , Humanos , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Programas Nacionales de Salud/estadística & datos numéricos , Análisis de Regresión , República de Corea , Reinserción al Trabajo , Adulto Joven
3.
Life Sci ; 147: 39-45, 2016 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-26820672

RESUMEN

AIMS: Sweetme Sweet Pumpkin™ (SSP, baked Cucurbita moschata Duch.) has been used to treat patients with depression in Korea. However, the role of SSP in improving depression has not been elucidated yet. Thus, we assessed the antidepressant-like effect of SSP and its active compound, ß-carotene, with the forced swimming test (FST). MAIN METHODS: SSP and ß-carotene were orally administered once a day for 28days. The levels of brain-derived neurotrophic factor (BDNF), phosphorylated extracellular signal-regulated kinase (pERK), and estrogen receptor-beta (ER-ß) were analyzed by Western blotting and quantitative real-time-polymerase chain reaction. KEY FINDINGS: After 28days, treatment with SSP and ß-carotene significantly decreased the immobility time during the FST. SSP significantly increased the levels of serotonin and norepinephrine in the brain. The levels of BDNF, pERK, and ER-ß were significantly increased in the SSP- and ß-carotene-administered groups compared with the control group. In addition, the groups treated with SSP and ß-carotene showed significantly reduced levels of tumor necrosis factor-alpha and interleukin-6 compared with the control group. SIGNIFICANCE: In conclusion, these findings suggest the potential of SSP and ß-carotene as a novel therapeutic agent for the treatment of depression.


Asunto(s)
Antidepresivos/farmacología , Cucurbita/química , Depresión/tratamiento farmacológico , beta Caroteno/farmacología , Animales , Antidepresivos/administración & dosificación , Factor Neurotrófico Derivado del Encéfalo/metabolismo , Modelos Animales de Enfermedad , Receptor beta de Estrógeno/metabolismo , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Interleucina-6/metabolismo , Masculino , Medicina Tradicional Coreana , Ratones , Ratones Endogámicos ICR , Norepinefrina/metabolismo , Fosforilación , Reacción en Cadena en Tiempo Real de la Polimerasa , Serotonina/metabolismo , Natación , Factor de Necrosis Tumoral alfa/metabolismo , beta Caroteno/administración & dosificación
4.
Mitochondrial DNA A DNA Mapp Seq Anal ; 27(6): 4342-4343, 2016 11.
Artículo en Inglés | MEDLINE | ID: mdl-26462716

RESUMEN

Epimedium koreanum is a perennial medicinal plant distributed in Eastern Asia. The complete chloroplast genome sequences of E. koreanum was obtained by de novo assembly using whole genome next-generation sequences. The chloroplast genome of E. koreanum was 157 218 bp in length and separated into four distinct regions such as large single copy region (89 600 bp), small single copy region (17 222 bp) and a pair of inverted repeat regions (25 198 bp). The genome contained a total of 112 genes including 78 protein-coding genes, 30 tRNA genes, and 4 rRNA genes. Phylogenetic analysis with the reported chloroplast genomes revealed that E. koreanum is most closely related to Berberis bealei, a traditional medicinal plant in the Berberidaceae family.


Asunto(s)
Epimedium/genética , Genoma del Cloroplasto/genética , Composición de Base/genética , Secuencia de Bases/genética , Berberidaceae/genética , Evolución Biológica , Cloroplastos/genética , Genes Mitocondriales/genética , Genes de Plantas/genética , Genoma/genética , Genoma Mitocondrial/genética , Genoma de Planta/genética , Mitocondrias/genética , Filogenia , Plantas Medicinales/genética , Análisis de Secuencia de ADN/métodos
5.
Arch Pharm Res ; 38(6): 1223-31, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-25163682

RESUMEN

Stillen has been used to treat patients with gastric mucosal ulcers and has an anti-inflammatory effect. It is well-known that neuro-inflammatory reactions are related to depression. Here we evaluated the antidepressant-like effect of Stillen on mice subjected to the forced swimming test (FST). Stillen and eupatilin (a major component of Stillen) significantly decreased immobility times compared with the FST control group. In the Stillen-administered group, increased levels of 5-hydroxytryptamine (serotonin) and brain-derived neurotrophic factor protein were observed in the hippocampus. Nissl bodies also increased in the hippocampus neuronal cytoplasm of the Stillen-administered group. Stillen decreased levels of interleukin (IL)-1ß, IL-6, and tumor necrosis factor-α (at the mRNA and protein levels) in the hippocampus and serum, compared with the control group. In addition, the mRNA expression of estrogen receptor-ß increased after Stillen administration in the hippocampus. These findings suggest that Stillen should be viewed as a candidate antidepressant.


Asunto(s)
Antidepresivos/farmacología , Extractos Vegetales/farmacología , Animales , Artemisia/química , Factor Neurotrófico Derivado del Encéfalo/metabolismo , Citocinas/metabolismo , Receptor beta de Estrógeno/biosíntesis , Flavonoides/farmacología , Hipocampo/citología , Hipocampo/efectos de los fármacos , Hipocampo/metabolismo , Interleucina-1beta/metabolismo , Interleucina-6/metabolismo , Masculino , Ratones , Ratones Endogámicos ICR , Actividad Motora/efectos de los fármacos , Neuronas/efectos de los fármacos , Neuronas/metabolismo , Serotonina/metabolismo , Natación/psicología , Factor de Necrosis Tumoral alfa/metabolismo
6.
J Antimicrob Chemother ; 49(1): 95-101, 2002 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11751772

RESUMEN

In the course of the search for inhibitors of ScCHS2 from natural sources, we have isolated a new type of chitin synthase 2 inhibitor, obovatol, which has a biphenol skeleton, from Magnolia obovata. Obovatol inhibited chitin synthase 2 activity of Saccharomyces cerevisiae with an IC(50) of 38 microM. Its derivative, tetrahydroobovatol, inhibited chitin synthase 2 activity under the same conditions with an IC(50) of 59 microM. These compounds exhibited no inhibitory activity for ScCHS3, and showed less inhibitory activity for chitin synthase 1 than for chitin synthase 2 (IC(50) > 1 mM). These results indicated that obovatol and tetrahydroobovatol are specific inhibitors of ScCHS2. They also inhibited CaCHS1, which is structurally and functionally analogous to ScCHS2, with similar IC(50)s to ScCHS2 (IC(50) 28 and 51 microM, respectively). The compounds exhibited mixed competitive inhibition with respect to UDP-N-acetyl-D-glucosamine as substrate [inhibition constant (K(i)) 21.8 microM for obovatol and 23.1 microM for tetrahydroobovatol]. Furthermore, they showed antifungal activities against various pathogenic fungi, with a particularly strong inhibitory activity against Cryptococcus neoformans (MIC 7.8 mg/L). The results indicate that obovatol and tetrahydroobovatol can potentially serve as antifungal agents.


Asunto(s)
Antifúngicos/farmacología , Compuestos de Bifenilo/farmacología , Quitina Sintasa/antagonistas & inhibidores , Inhibidores Enzimáticos/farmacología , Magnoliaceae/química , Éteres Fenílicos/farmacología , Saccharomyces cerevisiae/efectos de los fármacos , Antiinfecciosos/química , Antiinfecciosos/aislamiento & purificación , Antiinfecciosos/farmacología , Antifúngicos/química , Antifúngicos/aislamiento & purificación , Compuestos de Bifenilo/química , Compuestos de Bifenilo/aislamiento & purificación , Candida albicans/efectos de los fármacos , Candida albicans/enzimología , Quitina Sintasa/biosíntesis , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/aislamiento & purificación , Isoenzimas/antagonistas & inhibidores , Éteres Fenílicos/química , Éteres Fenílicos/aislamiento & purificación , Fitoterapia/métodos , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Hojas de la Planta/química , Saccharomyces cerevisiae/enzimología
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