RESUMEN
The response to treatment of severe methicillin-resistant Staphylococcus aureus (MRSA) infections with the traditional antibiotics is sometimes unsatisfactory and multiple antibiotic resistance is common. Adjuvant therapy such as intravenous immunoglobulin G (IVIG) could possibly be helpful in the treatment of such infections. The effect of IVIG on the capacity of human neutrophils to phagocytose and kill MRSA was investigated in vitro using the MTT assay and measuring the production of reactive oxygen species (ROS) and nitric oxide (NO). The efficiency of IVIG in neutralizing α-hemolysin and coagulase of MRSA was also assessed. The capability of IVIG in the treatment and prevention of MRSA infections was also evaluated in a murine peritonitis model. IVIG significantly enhanced (p < 0.01) the killing of MRSA by neutrophils at all concentrations tested (0.1-5 mg/ml) by 30-80 % of control values. It significantly (p < 0.01) increased the level of NO production in a dose-dependent manner, giving up to 60 µM at 5 mg/ml. The ROS level significantly increased (p < 0.01) in the presence of IVIG. In addition, IVIG significantly reduced the hemolytic activity of MRSA 10-fold and its coagulation capabilities by 50 %. When tested in vivo, groups receiving IVIG via tail vein infusion showed no significant improvement in their survival. Only when delivered to the same site of infection did IVIG show an improvement in the survival of mice (n = 80). These results could pave the way for a better understanding of the mechanism of action of IVIG and suggest its clinical potential as an adjuvant preventive and therapeutic agent against life-threatening infections caused by MRSA and other bacteria.
Asunto(s)
Inmunoglobulinas Intravenosas/uso terapéutico , Staphylococcus aureus Resistente a Meticilina/patogenicidad , Peritonitis/terapia , Infecciones Estafilocócicas/terapia , Animales , Antibacterianos/farmacología , Toxinas Bacterianas/inmunología , Coagulasa/inmunología , Proteínas Hemolisinas/inmunología , Humanos , Masculino , Staphylococcus aureus Resistente a Meticilina/inmunología , Staphylococcus aureus Resistente a Meticilina/aislamiento & purificación , Ratones , Pruebas de Sensibilidad Microbiana , Neutrófilos/inmunología , Óxido Nítrico/metabolismo , Oxacilina/farmacología , Peritonitis/inmunología , Peritonitis/microbiología , Especies Reactivas de Oxígeno/metabolismo , Infecciones Estafilocócicas/inmunologíaRESUMEN
The novel iridoid glycosides, isounedoside and grandifloric acid, were isolated from Thunbergia grandiflora. Grandifloric acid contains C-10 as a carboxylic acid group, the presence of which was predicted by recent iridoid biosynthesis studies carried out within T. alata. Isounedoside contains a rare 6,7-epoxide functional group. A revision in some of the NMR spectral assignments for the known iridoid glycoside alatoside was also made.
Asunto(s)
Diterpenos/química , Glucósidos/química , Plantas Medicinales , Piranos/química , Diterpenos/aislamiento & purificación , Glucósidos/aislamiento & purificación , Estructura Molecular , Extractos Vegetales , Piranos/aislamiento & purificaciónRESUMEN
The new phenylethanoid glycosides 2-O-acetyl-3'''-O-methylverbascoside and 2,4"-di-O-acetyl-3'''-O-methylverbascoside were isolated and identified from Penstemon crandallii. The major iridoid glycoside was plantarenaloside and no aucubin type iridoids were found. This contrasted with a previous analysis of P. teucrioides, from the same Penstemon subsection, which was dominated by aucubin derivatives.
Asunto(s)
Glucósidos/química , Glicósidos/química , Fenoles , Plantas/química , Conformación de Carbohidratos , Secuencia de Carbohidratos , Glucósidos/aislamiento & purificación , Glicósidos/aislamiento & purificación , Modelos Moleculares , Conformación Molecular , Datos de Secuencia Molecular , Estructura Molecular , Extractos Vegetales , Relación Estructura-ActividadRESUMEN
A phytochemical investigation of an ethanolic extract of the leaves of Curatella americana Linn. (Dilleniaceae) resulted in the isolation and identification of the flavonol glycoside avicularin and gallic acid.