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1.
EMBO Mol Med ; 8(4): 375-87, 2016 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-26941261

RESUMEN

Bone anabolic agents promoting bone formation and rebuilding damaged bones would ideally overcome the limitations of anti-resorptive therapy, the current standard prescription for osteoporosis. However, the currently prescribed parathyroid hormone (PTH)-based anabolic drugs present limitations and adverse effects including osteosarcoma during long-term use. Also, the antibody-based anabolic drugs that are currently being developed present the potential limits in clinical application typical of macromolecule drugs. We previously identified that CXXC5 is a negative feedback regulator of the Wnt/ß-catenin pathway via its interaction with Dishevelled (Dvl) and suggested the Dvl-CXXC5 interaction as a potential target for anabolic therapy of osteoporosis. Here, we screened small-molecule inhibitors of the Dvl-CXXC5 interaction via a newly established in vitro assay system. The screened compounds were found to activate the Wnt/ß-catenin pathway and enhance osteoblast differentiation in primary osteoblasts. The bone anabolic effects of the compounds were shown using ex vivo-cultured calvaria. Nuclear magnetic resonance (NMR) titration analysis confirmed interaction between Dvl PDZ domain and KY-02061, a representative of the screened compounds. Oral administration of KY-02327, one of 55 newly synthesized KY-02061 analogs, successfully rescued bone loss in the ovariectomized (OVX) mouse model. In conclusion, small-molecule inhibitors of the Dvl-CXXC5 interaction that block negative feedback regulation of Wnt/ß-catenin signaling are potential candidates for the development of bone anabolic anti-osteoporosis drugs.


Asunto(s)
Proteínas Dishevelled/antagonistas & inhibidores , Proteínas Dishevelled/metabolismo , Péptidos y Proteínas de Señalización Intracelular/antagonistas & inhibidores , Péptidos y Proteínas de Señalización Intracelular/metabolismo , Osteoporosis/tratamiento farmacológico , Administración Oral , Animales , Proteínas de Unión al ADN , Evaluación Preclínica de Medicamentos/métodos , Ratones , Técnicas de Cultivo de Órganos , Osteoblastos/efectos de los fármacos , Unión Proteica/efectos de los fármacos , Cráneo/efectos de los fármacos , Cráneo/crecimiento & desarrollo , Factores de Transcripción , Resultado del Tratamiento , Vía de Señalización Wnt/efectos de los fármacos
2.
Inflammation ; 33(2): 110-8, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19888641

RESUMEN

Radix Isatidis is the dried root of the plant Isatidis indigotica Fort (family Cruciferae) and traditionally used as an anti-viral, anti-bacterial, anti-endotoxic, and immune regulatory agent in the folk medicine of Korea and China. The aim of the present study was to determine the anti-inflammatory effects of methanolic extracts of Radix Isatidis (RIME) in lipopolysaccharide (LPS)-stimulated murine macrophages and in a TPA-induced ear edema animal model. Anti-inflammatory effects of RIME were examined in LPS-stimulated RAW 264.7 macrophages. In order to investigate the effects of RIME in vivo, activation of myeloperoxidase, and histological assessment were examined in the 12-O-tetradecanoyl-phorbol-13-acetate (TPA)-induced mouse ear edema model. RIME significantly inhibited the release from macrophages of inflammatory mediators such as nitric oxide, prostaglandin E(2), and pro-inflammatory cytokines. Topical administration of RIME at 1-5 mg/ear resulted in reduction of ear inflammation in mice. Thus, our results indicate that the anti-inflammatory effects of RIME involve decreased production of inflammatory mediators, which suggests that RIME may have therapeutic potential in a variety of inflammation-related diseases.


Asunto(s)
Antiinflamatorios/farmacología , Brassicaceae , Edema/prevención & control , Inflamación/prevención & control , Macrófagos/efectos de los fármacos , Extractos Vegetales/farmacología , Animales , Antiinflamatorios/aislamiento & purificación , Brassicaceae/química , Línea Celular , Supervivencia Celular/efectos de los fármacos , Dinoprostona/metabolismo , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Oído , Edema/inducido químicamente , Edema/inmunología , Femenino , Quinasa I-kappa B/metabolismo , Inflamación/inducido químicamente , Inflamación/inmunología , Mediadores de Inflamación/metabolismo , Interleucina-6/metabolismo , Lipopolisacáridos/farmacología , Macrófagos/inmunología , Metanol/química , Ratones , Ratones Endogámicos ICR , FN-kappa B/metabolismo , Óxido Nítrico/metabolismo , Peroxidasa/metabolismo , Extractos Vegetales/aislamiento & purificación , Raíces de Plantas , Solventes/química , Acetato de Tetradecanoilforbol , Factores de Tiempo , Factor de Necrosis Tumoral alfa/metabolismo
3.
Arch Pharm Res ; 26(2): 114-9, 2003 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-12643585

RESUMEN

A high performance liquid chromatographic (HPLC) method was developed for the qualitative and quantitative determination of benzophenanthridine alkaloids from the methanol extracts of Hylomecon hylomeconoides and H. vernale (Papaveraceae). Achiral and chiral methods were adapted for the separation of 6-methoxydihydrosanguinarine (1), 6-acetonyldihydrosanguinarine (2) and dihydrosanguinarine (3). The achiral reversed phase HPLC method made it possible the simultaneous separation and determination of 1, 2 and 3 within 20 min on ODS column using acetonitrile-phosphate buffer (50 mM, pH 7.0) (50:50, v/v). The separation and determination of 1 and 2 enantiomers was available using chiral columns. The same amount of (+) and (-)-enantiomers of 1 was found from the methanol extract of specimen, indicated that 1 could be the artifact produced by the reaction of sanguinarine with methanol. H. hylomeconoides showed higher level of 1 and 3 in compared with H. vernale, especially in root samples permitting the possibility of chemical discrimination between two species.


Asunto(s)
Alcaloides/aislamiento & purificación , Papaveraceae/química , Fenantridinas/aislamiento & purificación , Alcaloides/química , Cromatografía Líquida de Alta Presión , Metanol/química , Estructura Molecular , Fenantridinas/química , Extractos Vegetales/química , Raíces de Plantas/química , Estereoisomerismo
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