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1.
Mar Drugs ; 11(9): 3272-87, 2013 Aug 27.
Artículo en Inglés | MEDLINE | ID: mdl-23985898

RESUMEN

Sargassum muticum (S. muticum) is a brown edible alga and widely distributed in Korea. This report was designed to evaluate the anti-inflammatory properties of apo-9'-fucoxanthinone (APO-9') isolated from S. muticum on pro-inflammatory cytokine production. S. muticum extract (SME) exhibited significant inhibitory effects on pro-inflammatory cytokine production in bone marrow-derived macrophages (BMDMs) and dendritic cells (BMDCs). APO-9' pre-treatment in the CpG DNA-stimulated BMDMs and BMDCs showed a strong dose-dependent inhibitory effect on interleukin (IL)-12 p40, IL-6 and tumor necrosis factor (TNF)-α production with IC50 values ranging from 5.31 to 13.79. It exhibited a strong inhibitory effect on the phosphorylation of ERK1/2 and on activator protein (AP)-1 reporter activity. APO-9' pre-treatment exhibited significant inhibition of CpG DNA-induced production of inducible nitric oxide synthase. Taken together, these data suggest that SME and APO-9' have a significant anti-inflammatory property and warrant further studies concerning the potentials of SME and APO-9' for medicinal use.


Asunto(s)
Antiinflamatorios/química , Antiinflamatorios/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Sargassum/química , Animales , Línea Celular , Islas de CpG/efectos de los fármacos , Células HEK293 , Humanos , Proteínas I-kappa B/metabolismo , Interleucina-2/metabolismo , Interleucina-6/metabolismo , Macrófagos/efectos de los fármacos , Macrófagos/metabolismo , Ratones , Proteínas Quinasas Activadas por Mitógenos , Inhibidor NF-kappaB alfa , FN-kappa B/metabolismo , Óxido Nítrico Sintasa de Tipo II/metabolismo , Phaeophyceae/química , Fosforilación/efectos de los fármacos , Transducción de Señal/efectos de los fármacos , Factor de Transcripción AP-1/metabolismo
2.
Nat Prod Commun ; 8(4): 427-8, 2013 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-23738441

RESUMEN

This study was conducted to identify the anti-melanogenesis constituents from a seaweed Dictyota coriacea (Holmes). Three known compounds, viz. 1,9-dihydroxycrenulide (1), epiloliolide (2) and D-mannitol (3), were isolated from the ethanol extract. The melanin synthesis inhibition activities were evaluated using B16F10 melanoma cells for the isolates. Compared with the positive control, arbutin, compounds 1 and 2 exhibited more potency, showing 27.8 and 22.6% inhibition activities at a substrate concentration of 30 microg/mL. Our studies also indicate that these compounds are not cytotoxic. Hence, they might prove to be useful therapeutic agents for treating hyperpigmentation and effective components of whitening cosmetics.


Asunto(s)
Melaninas/antagonistas & inhibidores , Algas Marinas/química , Animales , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Melaninas/biosíntesis , Ratones
3.
In Vitro Cell Dev Biol Anim ; 48(10): 666-74, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23093465

RESUMEN

The aim of this study was to investigate the protective effects of the ethanol extract of the red algae Chondracanthus tenellus (Harvey) Hommersand (CTE) on cultured human keratinocyte cell line. The cellular protection conferred by CTE was evidenced by the ability of the extract to absorb ultraviolet B (UVB; 280-320 nm) and to scavenge the radical 1,1-diphenyl-2-picrylhydrazyl, as well as intracellular reactive oxygen species (ROS), induced by either hydrogen peroxide (H(2)O(2)) or UVB radiation. In addition, both superoxide anion generated by the xanthine/xanthine oxidase system and hydroxyl radical generated by the Fenton reaction (FeSO(4) + H(2)O(2)) were scavenged by CTE, as confirmed using electron spin resonance spectrometry. In the human keratinocyte cell line, CTE decreased the degree of injury resulting from UVB-induced oxidative stress to lipids, proteins, and DNA. CTE-treated cells also showed a reduction in UVB-induced apoptosis, as exemplified by fewer apoptotic bodies and less DNA fragmentation. Taken together, these results suggest that CTE confers protection on the human keratinocyte cell line against UVB-induced oxidative stress by absorbing UVB ray and scavenging ROS, thereby reducing injury to cellular constituents.


Asunto(s)
Radicales Libres , Queratinocitos/efectos de los fármacos , Extractos Vegetales/farmacología , Rhodophyta/química , Rayos Ultravioleta , Línea Celular , Espectroscopía de Resonancia por Spin del Electrón , Humanos
4.
Acta Microbiol Immunol Hung ; 57(1): 15-27, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20350876

RESUMEN

A number of essential oils from citrus peels are claimed to have biological activities. Citrus peel, called 'Jin-Pi', is used in traditional medicine for digestion, severe cold, and fever. However, the antibacterial activities against skin pathogens and anti-inflammatory effects of the essential oils of Citrus sunki (JinGyul) and Fortunella japonica var. margarita (GumGyul) have not yet been described. Therefore, in this study, the essential oils of the citrus species C. sunki (CSE) and F. japonica var. margarita (FJE), both native to the island of Jeju, Korea, were examined for their anti-inflammatory and antimicrobial activities against skin pathogens. Four human skin pathogenic microorganisms, Staphylococcus epidermidis CCARM 3709, Propionibacterium acnes CCARM 0081, Malassezia furfur KCCM 12679, and Candida albicans KCCM 11282, were studied. CSE and FJE exhibited strong antimicrobial activity against most of the pathogenic bacteria and yeast strains that were tested. Interestingly, CSE and FJE even showed antimicrobial activity against antibiotic-resistant S. epidermidis CCARM 3710, S. epidermidis CCARM 3711, P. acnes CCARM9009, and P. acnes CCARM9010 strains. In addition, CSE and FJE reduced the lipopolysaccharide (LPS)-induced secretion of nitric oxide (NO) in RAW 264.7 cells, indicating that they have anti-inflammatory effects. We also analysed the chemical composition of the oils by gas chromatography-mass spectrometry (GC-MS) and identified several major components, including dl-limonene (68.18%) and beta-myrcene (4.36%) for CSE, and dl-limonene (61.58%) and carvone (6.36%) for FJE. Taken together, these findings indicate that CSE and FJE have great potential to be used in human skin health applications.


Asunto(s)
Antiinfecciosos/farmacología , Candida albicans/efectos de los fármacos , Citrus/química , Malassezia/efectos de los fármacos , Óxido Nítrico/antagonistas & inhibidores , Aceites Volátiles/farmacología , Propionibacterium acnes/efectos de los fármacos , Rutaceae/química , Staphylococcus epidermidis/efectos de los fármacos , Animales , Antiinflamatorios/farmacología , Línea Celular , Dermatitis/microbiología , Relación Dosis-Respuesta a Droga , Farmacorresistencia Microbiana , Humanos , Macrófagos/efectos de los fármacos , Macrófagos/metabolismo , Ratones , Pruebas de Sensibilidad Microbiana , Óxido Nítrico/biosíntesis , Aceites Volátiles/química , República de Corea , Enfermedades Cutáneas Infecciosas/microbiología
5.
Phytother Res ; 24(6): 840-5, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19960418

RESUMEN

On Jeju Island, South Korea, the leaves of Eurya emarginata have been traditionally used to treat ulcers or as a diuretic. Eutigoside C isolated from the leaves has been reported to have in vitro anti-inflammatory effects. We evaluated the radioprotective effects of eutigoside C on jejunal cell apoptosis and crypt survival in mice subjected to gamma irradiation. In addition, the ability of eutigoside C to protect against radiation-induced oxidative stress was examined by evaluating the activities of superoxide dismutase (SOD) and catalase (CAT) in radiation-induced hepatic injury. Eutigoside C was administered intraperitoneally at 48, 12, and 1 h before irradiation. The administration of eutigoside C (10, 50, or 100 mg/kg body weight) before irradiation protected the intestinal crypts from radiation-induced apoptosis (p < 0.05), and attenuated radiation-induced decrease of villous height (p < 0.05). Pretreating mice prior to irradiation with eutigoside C (100 mg/kg) significantly improved the survival of the jejunal crypt (p < 0.01). The dose reduction factor was 1.09 at 3.5 days after irradiation. Treatment of eutigoside C prior to irradiation significantly protected SOD and CAT activities in radiation-induced hepatic injury (p < 0.05). These results suggest that eutigoside C is a useful radioprotector capable of defending intestinal progenitor cells against indirect depletion, such as oxidative stress and inflammatory response caused by gamma irradiation.


Asunto(s)
Glucósidos/farmacología , Intestinos/efectos de la radiación , Fenoles/farmacología , Traumatismos Experimentales por Radiación/tratamiento farmacológico , Protectores contra Radiación/farmacología , Animales , Apoptosis/efectos de los fármacos , Catalasa/metabolismo , Rayos gamma , Yeyuno/efectos de la radiación , Magnoliopsida/química , Masculino , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos ICR , Estrés Oxidativo/efectos de los fármacos , Fitoterapia , Superóxido Dismutasa/metabolismo
6.
Pol J Microbiol ; 58(1): 61-8, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19469288

RESUMEN

In this study, the chemical composition of Cryptomeria japonica essential oil (CJE) was analyzed and its biological activities were tested. CJE was obtained by steam distillation from leaves collected from Jeju Island and analyzed by gas chromatography (GC)-flame ionization detection (FID) and GC-MS. Kaurene (17.20%), elemol (10.88%), gamma-eudesmol (9.41%), and sabinene (8.86%) were the major components in CJE. The antibacterial and anti-inflammatory activities of CJE against drug-susceptible and -resistant skin pathogens have been not reported previously. Thus, we determined the anti-bacterial activities of CJE using the disk diffusion method and minimum inhibitory concentration (MIC) values. CJE showed excellent antibacterial activities against Propionibacterium acnes and Staphylococcus epidermidis, which are acne-causing bacteria. The MIC of CJE against drug-susceptible and -resistant P. acens and S. epidermidis ranged from 0.16 to 10.0 microl/ml. In addition, the effects of CJE on nitric oxide (NO), prostaglandin E2 (PGE2), tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, and IL-6 production in lipopolysaccharide (LPS)-activated RAW 264.7 macrophages were also examined. Pro-inflammatory cytokine and mediator tests indicated that CJE has excellent dose-dependent inhibitory activities. Therefore, based on these results, we propose that CJE is an attractive acne-mitigating candidate for skin health.


Asunto(s)
Acné Vulgar/tratamiento farmacológico , Cryptomeria , Citocinas/biosíntesis , Óxido Nítrico/biosíntesis , Fitoterapia , Aceites de Plantas/uso terapéutico , Propionibacterium acnes/efectos de los fármacos , Staphylococcus epidermidis/efectos de los fármacos , Acné Vulgar/patología , Animales , Línea Celular , Farmacorresistencia Bacteriana , Cromatografía de Gases y Espectrometría de Masas , Humanos , Inflamación/tratamiento farmacológico , Inflamación/metabolismo , Lipopolisacáridos/metabolismo , Ratones , Aceites de Plantas/química , Propionibacterium acnes/crecimiento & desarrollo , Staphylococcus epidermidis/crecimiento & desarrollo
7.
J Oleo Sci ; 57(11): 623-8, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18838835

RESUMEN

In this study, the chemical composition and anti-inflammatory activities of hydrodistilled essential oil from Farfugium japonicum were investigated for the first time. The chemical constituents of the essential oil were further analyzed by GC-MS and included 1-undecene (22.43%), 1-nonene (19.83%), beta-caryophyllene (12.26%), alpha-copaene (3.70%), gamma-curcumene (2.86%), germacrene D (2.69%), and 1-decene (2.08%). The effects of the essential oil on nitric oxide (NO) and prostaglandin E2 (PGE(2)) production in lipopolysaccharide (LPS)-activated RAW 264.7 macrophages were also examined. The results indicate that the F. japonicum essential oil is an effective inhibitor of LPS-induced NO and PGE(2) production in RAW 264.7 cells. These inhibitory effects of the F. japonicum essential oil were accompanied by dose-dependent decreases in the iNOS and COX-2 mRNA expression. In order to determine whether F. japonicum essential oil can safely be applied to human skin, the cytotoxic effects of F. japonicum essential oil were determined by colorimetric MTT assays in human dermal fibroblast and keratinocyte HaCaT cells. F. japonicum essential oil exhibited low cytotoxicity at 100 mug/mL. Based on these results, we suggest that F. japonicum essential oil may be considered a potential anti-inflammatory candidate for topical application.


Asunto(s)
Antiinflamatorios/farmacología , Asteraceae/química , Flores/química , Aceites de Plantas/análisis , Aceites de Plantas/farmacología , Animales , Línea Celular , Ciclooxigenasa 2/biosíntesis , Dinoprostona/biosíntesis , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Fibroblastos/enzimología , Regulación Enzimológica de la Expresión Génica/efectos de los fármacos , Humanos , Lipopolisacáridos/farmacología , Macrófagos/enzimología , Ratones , Óxido Nítrico/biosíntesis , Óxido Nítrico Sintasa de Tipo II/biosíntesis , ARN Mensajero/biosíntesis
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