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1.
BMC Complement Altern Med ; 15: 424, 2015 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-26627190

RESUMEN

BACKGROUND: Suo Quan Wan (SQW) is a Chinese traditional prescription that has been used in clinical treatment of lower urinary tract symptoms for centuries. However, scientific basis of SQW efficacy and mechanism is still needed. This study investigated the effect of SQW on bladder function and transient receptor potential vanilloid 1 (TRPV1) expression in the bladder of rats with bladder outlet obstruction (BOO). The induced changes in bladder function in overactive bladder (OAB) rat model were observed following different periods of outlet obstruction to obtain an appropriate rat model. METHODS: This study was carried out in two parts. In the first part, female Sprague-Dawley rats received sham operations or partial BOO operations. Two, four, and six weeks later, the OAB model groups and control were subjected to urodynamic tests to measure differences in bladder functions. Once the appropriate rat model was obtained, the second part of the experiment was performed. The rat model was recreated and treated with SQW. Urodynamic assessment was conducted, and the bladders of the rats were then removed. Immunofluorescence staining, real-time PCR, and Western blot were performed to localize and quantify the expression of TRPV1 in the bladder. RESULTS: Results of the first part indicated that at 2 and 4 weeks, the OAB model group exhibited significant differences in urodynamic parameters, including bladder pressure, maximum voiding pressure, and maximum bladder capacity, compared with the sham group. At 4 and 6 weeks, the OAB model group exhibited significant differences in residual volume (RV) and non-voiding contraction frequency. Six-week OAB model group showed much more RV but less voiding efficiency when compared with 6-week sham group or 2-and 4-week OAB model group. Rats that underwent BOO exhibited similarities with the compensated state before four weeks and may have entered decompensated state at six weeks. Studies conducted with 4-week OAB model were appropriate. In part two of the experiment, unstable bladder in the OAB model group recovered bladder stability after SQW treatment, accompanied by improved bladder hypertrophy, as well as corrected urodynamic parameters. Expression of TRPV1 mRNA and proteins in the bladder was significantly greater in the OAB model group than that in the control group, which subsequently decreased significantly with SQW treatment in BOO-induced rats. CONCLUSIONS: SQW can modulate the expression of TRPV1 in accordance with the recovery of bladder function.


Asunto(s)
Medicamentos Herbarios Chinos/farmacología , Canales Catiónicos TRPV/biosíntesis , Obstrucción del Cuello de la Vejiga Urinaria/tratamiento farmacológico , Vejiga Urinaria/efectos de los fármacos , Animales , Modelos Animales de Enfermedad , Femenino , Medicina Tradicional China , Ratas , Ratas Sprague-Dawley , Vejiga Urinaria/metabolismo , Vejiga Urinaria/cirugía , Obstrucción del Cuello de la Vejiga Urinaria/metabolismo , Obstrucción del Cuello de la Vejiga Urinaria/fisiopatología , Vejiga Urinaria Hiperactiva/tratamiento farmacológico , Vejiga Urinaria Hiperactiva/metabolismo , Urodinámica
2.
ACS Appl Mater Interfaces ; 8(44): 30256-30263, 2016 Nov 09.
Artículo en Inglés | MEDLINE | ID: mdl-27767295

RESUMEN

Carbon coated SnS/SnO2 heterostructures wrapping on carbon nanofibers (C@SnS/SnO2@CNFs) was demonstrated to have excellent performance as an anode material for Li-ion batteries. C@SnS/SnO2@CNFs electrode delivers high reversible capacity of 826.8 mA h g-1 (500th cycle) at the current density of 1.0 A g-1. However, an interesting phenomenon of increasing capacity on cycling can be observed. According to the analysis of the evolution of structure and electrochemical property, C@SnS/SnO2@CNFs is demonstrated to experience the progress of conversion from nanowalls containing polycrystals into amorphous nanosheets with high porosity and larger surface upon cycling. The above lithiation-induced structural optimization provides larger effective surface areas and encourages the conversion reactions, which can promote charge transfer and also enhance the reversibility of the conversion reactions of SnS and SnO2 inducing the increasing reversible capacity. The study explains the progress of increasing capacity of C@SnS/SnO2@CNFs and likewise provides a perspective on optimization of the electrochemical performance of electrodes.

3.
Exp Ther Med ; 12(3): 1681-1692, 2016 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-27588088

RESUMEN

Grape seed proanthocyanidin (GSPA) consists of catechin, epicatechin and epicatechin gallate, which are strong antioxidants that are beneficial to health and may attenuate or prevent Alzheimer's disease (AD). In the present study, the effects of GSPA on pheochromocytoma (PC12) cell viability were determined using cell counting kit-8 and lactate dehydrogenase (LDH) assays, whereas apoptosis and mitochondrial membrane potential (Ψm) were measured via flow cytometry analysis. The effect of GSPA administration on the behavior and memory of amyloid precursor protein (APP)/presenilin-1 (PS-1) double transgenic mice was assessed using a Morris water maze. APP Aß peptides and tau hyperphosphorylation were examined by western blotting; whereas the expression levels of PS-1 were evaluated by reverse transcription-quantitative polymerase chain reaction and compared with pathological sections stained with hematoxylin-eosin and Congo red. Data from the in vitro experiments demonstrated that GSPA significantly alleviated Aß25-35 cytotoxicity and LDH leakage ratio, inhibited apoptosis and increased Ψm. The findings from the in vivo experiments showed a significant enhancement in cognition and spatial memory ability, an improvement in the pathology of APP and tau protein and a decrease in PS-1 mRNA expression levels. Therefore, the results of the present study indicated that GSPA may be a novel therapeutic strategy for the treatment of AD or may, at the very least, improve the quality of life of patients with AD.

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