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1.
J Nanobiotechnology ; 22(1): 148, 2024 Apr 03.
Artículo en Inglés | MEDLINE | ID: mdl-38570776

RESUMEN

Kaempferol (KA), an natural antioxidant of traditional Chinese medicine (TCM), is extensively used as the primary treatment for inflammatory digestive diseases with impaired redox homeostasis. Severe acute pancreatitis (SAP) was exacerbated by mitochondrial dysfunction and abundant ROS, which highlights the role of antioxidants in targeting mitochondrial function. However, low bioavailability and high dosage of KA leading to unavoidable side effects limits clinical transformation. The mechanisms of KA with poor bioavailability largely unexplored, hindering development of the efficient strategies to maximizing the medicinal effects of KA. Here, we engineered a novel thioketals (TK)-modified based on DSPE-PEG2000 liposomal codelivery system for improving bioavailability and avoiding side effects (denotes as DSPE-TK-PEG2000-KA, DTM@KA NPs). We demonstrated that the liposome exerts profound impacts on damaging intracellular redox homeostasis by reducing GSH depletion and activating Nrf2, which synergizes with KA to reinforce the inhibition of inadequate fission, excessive mitochondrial fusion and impaired mitophagy resulting in inflammation and apoptosis; and then, the restored mitochondrial homeostasis strengthens ATP supply for PAC renovation and homeostasis. Interestingly, TK bond was proved as the main functional structure to improve the above efficacy of KA compared with the absence of TK bond. Most importantly, DTM@KA NPs obviously suppresses PAC death with negligible side effects in vitro and vivo. Mechanismly, DTM@KA NPs facilitated STAT6-regulated mitochondrial precursor proteins transport via interacting with TOM20 to further promote Drp1-dependent fission and Pink1/Parkin-regulated mitophagy with enhanced lysosomal degradation for removing damaged mitochondria in PAC and then reduce inflammation and apoptosis. Generally, DTM@KA NPs synergistically improved mitochondrial homeostasis, redox homeostasis, energy metabolism and inflammation response via regulating TOM20-STAT6-Drp1 signaling and promoting mitophagy in SAP. Consequently, such a TCM's active ingredients-based nanomedicine strategy is be expected to be an innovative approach for SAP therapy.


Asunto(s)
Quempferoles , Pancreatitis , Humanos , Enfermedad Aguda , Quempferoles/farmacología , Quempferoles/metabolismo , Proteínas Quinasas/metabolismo , Proteínas Quinasas/farmacología , Pancreatitis/tratamiento farmacológico , Pancreatitis/metabolismo , Mitocondrias/metabolismo , Proteínas Mitocondriales/metabolismo , Inflamación/metabolismo
2.
Ital J Pediatr ; 44(1): 65, 2018 Jun 05.
Artículo en Inglés | MEDLINE | ID: mdl-29871689

RESUMEN

BACKGROUND: Most Neonatal Intensive Care Units (NICUs) in China have restricted visiting policies for parents. This also implicates that parents are not involved in the care of their infant. Family Integrated Care (FIC), empowering parents in direct care delivery and decisions, is becoming the standard in NICUs in many countries and can improve quality-of-life and health outcomes of preterm infants. The aim of this study was to evaluate the impact of a FIC intervention on the clinical outcomes of preterm infants with Bronchopulmonary Dysplasia (BPD). METHODS: A pre-post intervention study was conducted at NICUs in two Chinese children's hospitals. Infants with BPD were included: pre-intervention group (n = 134) from December 2015 to September 2016, post-intervention (FIC) group (n = 115) and their parents from October 2016 to June 2017. NICU nurses were trained between July and September 2016 to deliver the FIC intervention, including parent education and support. Parents had to be present and care for their infant minimal three hours a day. The infants' outcome measures were length-of-stay, breastfeeding, weight gain, respiratory and oxygen support, and parent hospital expenses. RESULTS: Compared with control group (n = 134), the FIC group (n = 115) had significantly increased breastfeeding rates (83% versus 71%, p = 0.030), breastfeeding time (31 days versus 19 days, p < 0.001), enteral nutrition time (50 days versus 34 days, p < 0.001), weight gain (29 g/day versus 23 g/day, p = 0.002), and significantly lower respiratory support time (16 days versus 25 days, p < 0.001). Oxygen Exposure Time decreased but not significant (39 days versus 41 days p = 0.393). Parents hospital expenses in local Chinese RMB currency was not significant (84 K versus 88 K, p = 0.391). CONCLUSION: The results of our study suggests that FIC is feasible in two Chinese NICUs and might improve clinical outcomes of preterm infants with BPD. Further research is needed to include all infants admitted to NICUs and should include parent reported outcome measures. Our study may help other NICUs with limited parental access to implement FIC to enhance parental empowerment and involvement in the care of their infant.


Asunto(s)
Displasia Broncopulmonar/terapia , Prestación Integrada de Atención de Salud/organización & administración , Enfermería de la Familia/organización & administración , Recien Nacido Prematuro , Unidades de Cuidado Intensivo Neonatal/organización & administración , Displasia Broncopulmonar/diagnóstico , Displasia Broncopulmonar/mortalidad , Estudios de Casos y Controles , China , Familia , Femenino , Hospitales Pediátricos , Humanos , Recién Nacido , Masculino , Evaluación de Resultado en la Atención de Salud , Desarrollo de Programa , Evaluación de Programas y Proyectos de Salud , Valores de Referencia , Estudios Retrospectivos , Medición de Riesgo , Análisis de Supervivencia
3.
Fitoterapia ; 109: 106-12, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26688377

RESUMEN

Five new caged polyprenylated xanthones (1a, 2a, 3, 10a and 10b), and 12 known related compounds were isolated from the resin of Garcinia hanburyi. Their structures were elucidated by detailed spectroscopic analyses and their α-glucosidase inhibitory activities were investigated in vitro. Most of xanthones showed modest inhibitory activity against α-glucosidase.


Asunto(s)
Garcinia/química , Inhibidores de Glicósido Hidrolasas/química , Resinas de Plantas/química , Xantonas/química , Inhibidores de Glicósido Hidrolasas/aislamiento & purificación , Estructura Molecular , Saccharomyces cerevisiae/enzimología , Xantonas/aislamiento & purificación , alfa-Glucosidasas/metabolismo
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