Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
Más filtros

Métodos Terapéuticos y Terapias MTCI
Bases de datos
País/Región como asunto
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
J Sci Food Agric ; 101(6): 2491-2499, 2021 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-33063324

RESUMEN

BACKGROUND: Codonopsis pilosula and C. tangshen are both plants widely used in traditional Chinese medicine. Polysaccharides, which are their primary active components, are thought to be important in their extensive use. In this study, two neutral polysaccharide fractions of C. pilosula (CPPN) and C. tangshen (CTPN) were obtained by fractionation on a DEAE-Sepharose column and characterized. RESULTS: It was confirmed that the neutral polymers CPPN and CTPN were ß-(2,1)-linked inulin-type fructans with non-reducing terminal glucose, and degree of polymerization (DP) of 19.6 and 25.2, respectively. The antioxidant and prebiotic activities in vitro were assayed based on IPEC-J2 cell lines and five strains of Lactobacillus. Results indicated that the effects of CPPN and CTPN were increased antioxidant defense in intestinal epithelial cells through enhanced cell viability, improved expression of total antioxidant capacity, glutathione peroxidase, superoxide dismutase and catalase, and reduced levels of malondialdehyde and lactic dehydrogenase. The prebiotic activity of CPPN and CTPN was demonstrated by the promoting effect on Lactobacillus proliferation in vitro. The different biological activities obtained between the two fractions are probably due to the different DP and thus molecular weights of CPPN and CTPN. CONCLUSION: The inulin fractions from C. pilosula and C. tangshen were natural sources of potential intestinal antioxidants as well as prebiotics, which will be valuable in further studies and new applications of inulin-containing health products. © 2020 Society of Chemical Industry.


Asunto(s)
Antioxidantes/química , Codonopsis/química , Medicamentos Herbarios Chinos/química , Fructanos/química , Inulina/química , Prebióticos/análisis , Antioxidantes/aislamiento & purificación , Antioxidantes/farmacología , Línea Celular , Supervivencia Celular/efectos de los fármacos , Codonopsis/clasificación , Medicamentos Herbarios Chinos/aislamiento & purificación , Medicamentos Herbarios Chinos/farmacología , Células Epiteliales/citología , Células Epiteliales/efectos de los fármacos , Células Epiteliales/metabolismo , Fructanos/aislamiento & purificación , Fructanos/farmacología , Humanos , Inulina/aislamiento & purificación , Inulina/farmacología , Lactobacillus/efectos de los fármacos , Lactobacillus/crecimiento & desarrollo , Estrés Oxidativo/efectos de los fármacos , Polimerizacion
2.
Molecules ; 24(20)2019 Oct 09.
Artículo en Inglés | MEDLINE | ID: mdl-31600890

RESUMEN

In this study, an acidic polysaccharide from Codonopsis pilosula Nannf. var. modesta (Nannf.) L. T. Shen (WCP-I) and its main fragment, WCP-Ia, obtained after pectinase digestion, were structurally elucidated and found to consist of a rhamnogalacturonan I (RG-I) region containing both arabinogalactan type I (AG-I) and type II (AG-II) as sidechains. They both expressed immunomodulating activity against Peyer's patch cells. Endo-1,4-ß-galactanase degradation gave a decrease of interleukine 6 (IL-6) production compared with native WCP-I and WCP-Ia, but exo-α-l-arabinofuranosidase digestion showed no changes in activity. This demonstrated that the stimulation activity partly disappeared with removal of ß-d-(1→4)-galactan chains, proving that the AG-I side chain plays an important role in immunoregulation activity. WCP-Ia had a better promotion effect than WCP-I in vivo, shown through an increased spleen index, higher concentrations of IL-6, transforming growth factor-ß (TGF-ß), and tumor necrosis factor-α (TNF-α) in serum, and a slight increment in the secretory immunoglobulin A (sIgA) and CD4+/CD8+ T lymphocyte ratio. These results suggest that ß-d-(1→4)-galactan-containing chains in WCP-I play an essential role in the expression of immunomodulating activity. Combining all the results in this and previous studies, the intestinal immune system might be the target site of WCP-Ia.


Asunto(s)
Codonopsis/química , Factores Inmunológicos/farmacología , Inmunomodulación/efectos de los fármacos , Extractos Vegetales/farmacología , Polisacáridos/farmacología , Animales , Supervivencia Celular/efectos de los fármacos , Hidrólisis , Inmunidad Mucosa/efectos de los fármacos , Factores Inmunológicos/química , Ratones , Estructura Molecular , Monosacáridos/química , Ganglios Linfáticos Agregados/efectos de los fármacos , Ganglios Linfáticos Agregados/inmunología , Ganglios Linfáticos Agregados/metabolismo , Extractos Vegetales/química , Polisacáridos/química , Análisis Espectral
3.
Molecules ; 22(2)2017 Feb 14.
Artículo en Inglés | MEDLINE | ID: mdl-28216596

RESUMEN

Rhizome of Ligusticum chuanxiong is an effective medical plant, which has been extensively applied for centuries in migraine and cardiovascular diseases treatment in China. Polysaccharides from this plant have been shown to have interesting bioactivities, but previous studies have only been performed on the neutral polysaccharides. In this study, LCP-I-I, a pectic polysaccharide fraction, was obtained from the 100 °C water extracts of L. chuangxiong rhizomes and purified by diethylaminethyl (DEAE) sepharose anion exchange chromatography and gel filtration. Monosaccharide analysis and linkage determination in addition to Fourier transform infrared (FT-IR) spectrometer and Nuclear magnetic resonance (NMR) spectrum, indicated that LCP-I-I is a typical pectic polysaccharide, with homo-galacturonan and rhamnogalacturonan type I regions and arabinogalactan type I and type II (AG-I/AG-II) side chains. LCP-I-I exhibited potent complement fixation activity, ICH50 of 26.3 ± 2.2 µg/mL, and thus has potential as a natural immunomodulator.


Asunto(s)
Activación de Complemento , Medicamentos Herbarios Chinos/química , Ligusticum/química , Pectinas/química , Cromatografía DEAE-Celulosa , Cromatografía de Gases , Pruebas de Fijación del Complemento , Galactanos/química , Cromatografía de Gases y Espectrometría de Masas , Espectroscopía de Resonancia Magnética , Peso Molecular , Monosacáridos/química , Plantas Medicinales/química , Rizoma/química , Espectroscopía Infrarroja por Transformada de Fourier
4.
Environ Toxicol Pharmacol ; 40(2): 388-96, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-26245812

RESUMEN

Chinese patent medicines play an important role in veterinary clinical use. The aim of this study is to research the anti-infection effect of Chinese patent medicine "Wuhuanghu" for the treatment of porcine infectious pleuropneumonia and to evaluate the safety of "Wuhuanghu" in order to provide a comprehensive understanding of its toxicity. The anti-infection results showed that the treatment with "Wuhuanghu" could significantly inhibit pneumonia and decrement of the pneumonia in high, medium and low doses of "Wuhuanghu" groups were 70.97%, 61.29% and 58.06% respectively. The acute toxicity test showed that rats in the highest group (5000mg/kg) had no death and no abnormal response, suggesting the LD50 of "Wuhuanghu" was more than 5000mg/kg. The subchronic toxicity study showed that hematology indexes in all groups had no obvious differences; blood biochemical index, only albumin and total cholesterol in middle and low doses of "Wuhuanghu" groups were significantly decreased when compared with control group. The clinical pathology showed that the target organ of "Wuhuanghu" was liver. The safety pharmacology study indicated that "Wuhuanghu" had no side effects on rats. In conclusion, "Wuhuanghu" has therapeutic and protective effects to porcine infectious pleuropneumonia in a dose-dependent manner and "Wuhuanghu" is a safe veterinary medicine.


Asunto(s)
Medicamentos Herbarios Chinos/administración & dosificación , Medicamentos sin Prescripción/administración & dosificación , Pleuroneumonía/veterinaria , Enfermedades de los Porcinos/tratamiento farmacológico , Animales , Relación Dosis-Respuesta a Droga , Medicamentos Herbarios Chinos/efectos adversos , Femenino , Hígado/efectos de los fármacos , Masculino , Medicamentos sin Prescripción/efectos adversos , Pleuroneumonía/tratamiento farmacológico , Pleuroneumonía/patología , Ratas , Porcinos , Enfermedades de los Porcinos/patología , Pruebas de Toxicidad Aguda , Pruebas de Toxicidad Subcrónica , Drogas Veterinarias/administración & dosificación , Drogas Veterinarias/efectos adversos
5.
Environ Toxicol Pharmacol ; 35(2): 240-6, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23353547

RESUMEN

Neem (Azadirachta indica), popularly known as traditional medicine is a native plant in India. Neem oil is a vegetable oil derived from seeds or fruits of the neem tree through pressing or solvent extraction, and largely used in popular medicine to have antifungal, antibacterial, antimalarial, antiparasitic, anti-inflammatory, as well as immunemodulatory properties in different animal species. In the present study, acute and 28-day subacute toxicity tests were carried out. In the acute toxicity test, the LD50 values of neem oil were found to be 31.95g/kg. The subacute treatment with neem oil failed to change body weight gain, food and water consumption. Serum biochemistry analysis showed no significant differences in any of the parameters examined under the dose of 1600mg/kg/day. Histopathological exams showed that the target organs of neem oil were testicle, liver and kidneys up to the dose of 1600mg/kg/day.


Asunto(s)
Azadirachta/toxicidad , Glicéridos/toxicidad , Terpenos/toxicidad , Animales , Azadirachta/química , Peso Corporal/efectos de los fármacos , Evaluación Preclínica de Medicamentos , Ingestión de Alimentos/efectos de los fármacos , Femenino , Glicéridos/farmacocinética , India , Riñón/efectos de los fármacos , Dosificación Letal Mediana , Hígado/efectos de los fármacos , Masculino , Ratones , Plantas Medicinales/química , Semillas/química , Terpenos/farmacocinética , Testículo/efectos de los fármacos , Distribución Tisular , Pruebas de Toxicidad Aguda , Pruebas de Toxicidad Subaguda
6.
Immunopharmacol Immunotoxicol ; 35(2): 215-24, 2013 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-23171279

RESUMEN

Xiang-Qi-Tang (XQT) is a Chinese herbal formula containing Cyperus rotundus, Astragalus membranaceus and Andrographis paniculata. Alpha-Cyperone (CYP), astragaloside IV (AS-IV) and andrographolide (AND) are the three major active components in this formula. XQT may modulate the inflammatory or coagulant responses. We therefore assessed the effects of XQT on lipopolysaccharide (LPS)-induced inflammatory model of rat cardiac microvascular endothelial cells (RCMECs). XQT, CYP, AS-IV and AND inhibited the production of tumor necrosis factor alpha (TNF-α), intercellular cell adhesion molecule-1 (ICAM-1) and plasminogen activator inhibitor-1 (PAI-1), and up-regulated the mRNA expression of Kruppel-like factor 2 (KLF2). XQT and CYP inhibited the secretion of tissue factor (TF). To further explore the mechanism, we found that XQT, or its active components CYP, AS-IV and AND significantly inhibited extracellular signal-regulated kinase (ERK), c-jun NH2-terminal kinase (JNK) and p38 phosphorylation protein expression as well as decreased the phosphorylation levels of nuclear factor κB (NF-κB) p65 proteins in LPS-stimulated RCMECs. These results suggested that XQT and its active components inhibited the expression of inflammatory and coagulant mediators via mitogen-activated protein kinase (MAPKs) and NF-κB signaling pathways. These findings may contribute to future research on the action mechanisms of this formula, as well as therapy for inflammation- or coagulation-related diseases.


Asunto(s)
Antiinflamatorios/farmacología , Anticoagulantes/farmacología , Medicamentos Herbarios Chinos/farmacología , Endotelio Vascular/efectos de los fármacos , Inflamación/tratamiento farmacológico , Lipopolisacáridos/farmacología , Proteínas Quinasas Activadas por Mitógenos/antagonistas & inhibidores , FN-kappa B/antagonistas & inhibidores , Animales , Células Endoteliales/efectos de los fármacos , Células Endoteliales/metabolismo , Endotelio Vascular/metabolismo , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Corazón/efectos de los fármacos , Inflamación/metabolismo , Molécula 1 de Adhesión Intercelular/metabolismo , Proteínas Quinasas JNK Activadas por Mitógenos/metabolismo , Factores de Transcripción de Tipo Kruppel/metabolismo , Microvasos/efectos de los fármacos , Microvasos/metabolismo , Proteínas Quinasas Activadas por Mitógenos/metabolismo , FN-kappa B/metabolismo , Fosforilación/efectos de los fármacos , Inhibidor 1 de Activador Plasminogénico/metabolismo , Ratas , Ratas Wistar , Transducción de Señal/efectos de los fármacos , Tromboplastina/metabolismo , Factor de Necrosis Tumoral alfa/metabolismo , Proteínas Quinasas p38 Activadas por Mitógenos/metabolismo
7.
Fitoterapia ; 84: 303-7, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23266729

RESUMEN

Ginsenoside Rh2 is one of the most important ginsenosides in ginseng with antitumor, antidiabetic, antiallergic, and anti-inflammatory effects. However, the extremely poor oral bioavailability induced by its low water solubility greatly limits the potency of Rh2 in clinical use. Therefore, in this study we sulfated 20(S)-ginsenoside Rh2 with chlorosulfonic acid and pyridine method, and got two new sulfated derivatives, Rh2-B1 and Rh2-B2, with higher water solubility. Their chemical structures were characterized by spectroscopic methods (IR, MS and NMR). Additionally, Rh2-B1 and Rh2-B2 had the greater anti-inflammatory effects than Rh2 through inhibiting inflammatory cytokines and mediators in LPS-induced mouse RAW264.7 macrophages cells. These results suggested that the sulfated modification of Rh2 improved its water solubility and the sulfated derivatives could be more potential candidates for developing as anti-inflammatory agents.


Asunto(s)
Citocinas/metabolismo , Regulación de la Expresión Génica/efectos de los fármacos , Ginsenósidos/química , Ginsenósidos/farmacología , Lipopolisacáridos/toxicidad , Macrófagos/efectos de los fármacos , Animales , Línea Celular , Citocinas/genética , Macrófagos/metabolismo , Ratones
8.
Immunopharmacol Immunotoxicol ; 34(5): 786-93, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22303901

RESUMEN

The present study was performed to investigate the effects of Jin-Ying-Tang (JYT), a Chinese herbal formula containing Lonicera japonica, Herba taraxaci, Fructus trichosanthis, Fructus forsythia, Radix et rhizoma rhei, Astragalus membranaceus, Angelica sinensis, on rabbit mastitis induced by Staphylococcus aureus. Suckling rabbits were challenged with 1.5 × 10(7) colony forming unit (CFU) of S. aureus at the base of the third pair teats, and they were treated and pretreated with JYT to detect the formula effects. The results showed that JYT could reduce the occurrence of Staphylococcal mastitis in rabbit model. To further investigate the action mechanism of JYT, we examined the leukocyte counts and inflammatory mediator levels such as TNF-α and IL-6 in blood and infected tissue. From histological study and blood analysis, we found that JYT could suppress leukocyte infiltration in infected mammary gland tissue and significantly inhibit the total leukocyte counts and lymphocytes (LYM), monocytes (MON) and granulocytes (GRA) fractions of leukocyte counts in blood. Enzyme-linked immunosorbent assay (ELISA) results showed JYT significantly decreased the TNF-α and IL-6 concentrations in serum and mammary gland. The analysis of these data suggested that JYT effectively inhibited inflammatory responses to reduce the occurrence of mastitis in rabbit model.


Asunto(s)
Medicamentos Herbarios Chinos/farmacología , Mastitis/tratamiento farmacológico , Infecciones Estafilocócicas/tratamiento farmacológico , Staphylococcus aureus , Animales , Femenino , Interleucina-6/sangre , Recuento de Leucocitos , Mastitis/sangre , Conejos , Infecciones Estafilocócicas/sangre , Factor de Necrosis Tumoral alfa/sangre
9.
Biol Pharm Bull ; 34(3): 379-82, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21372388

RESUMEN

Xiang-qi-tang (XQT) is a Chinese herbal formula containing rhizoma Cyperi, Andrographis paniculata and Astragalus membranaceus. The present study investigated the effects of XQT on the mortality and inflammatory mediators in a chicken model challenged with avian pathogenic Escherichia coli (APEC). To detect the effect of XQT, the chickens were pretreated with the formula 12 h before being challenged with 10(8) colony forming unit (CFU) of APEC. The results showed that 0.6 g/kg XQT significantly elevated the survival rate of infected chickens. To further investigate the mechanism of decreasing mortality of XQT, we examined plasma inflammatory mediator levels. The levels of tumor necrosis factor alpha (TNF-α), interleukin-1 (IL-1) and soluble endothelial protein C receptor (sEPCR) were significantly increased in chickens challenged with APEC alone, whereas chickens pretreated with 0.6 g/kg XQT showed marked decrease of these inflammatory mediator levels during the death peak. Taken together, this study demonstrates that XQT has protective effects in APEC-treated chickens. The action mechanisms of XQT involve anti-inflammation and antithrombotic activity. These findings may contribute to future research on the action mechanisms of this formula, as well as prevention of or therapy for avian colibacillosis.


Asunto(s)
Antiinflamatorios/uso terapéutico , Pollos , Medicamentos Herbarios Chinos/uso terapéutico , Infecciones por Escherichia coli/veterinaria , Fibrinolíticos/uso terapéutico , Mediadores de Inflamación/sangre , Enfermedades de las Aves de Corral/tratamiento farmacológico , Animales , Antiinflamatorios/farmacología , Factores de Coagulación Sanguínea , Medicamentos Herbarios Chinos/farmacología , Infecciones por Escherichia coli/sangre , Infecciones por Escherichia coli/tratamiento farmacológico , Infecciones por Escherichia coli/mortalidad , Fibrinolíticos/farmacología , Interleucina-1/sangre , Fitoterapia , Plantas Medicinales , Enfermedades de las Aves de Corral/sangre , Enfermedades de las Aves de Corral/microbiología , Enfermedades de las Aves de Corral/mortalidad , Receptores de Superficie Celular/sangre , Factor de Necrosis Tumoral alfa/sangre
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA