Yttrium oxide nanoflowers were prepared by a hydrothermal technique, and X-ray diffraction and scanning electron microscopy were used to determine their structures. The cytotoxic and genotoxic potentials of aqueous dispersions of the nanoflowers to cultured primary rat hepatocytes were examined at concentrations up to 500 mg L?1 for 72 h. Cell viability was determined by monitoring the reduction of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, release of lactate dehydrogenase, and uptake of neutral red. Genotoxicity was assessed by the liver micronucleus assay. Exposure to Y2O3 nanoflowers at concentrations lower than 100 mg L?1 did not lead to any cytotoxicity or genotoxicity. At higher concentrations (200, 400, and 500 mg L?1), cell viability decreased and induction of micronuclei increased (400 and 500 mg L?1). 相似文献
Hyperbaric oxygen increases the partial pressure of O2 in arterial blood and tissues and thereby relieves cellular hypoxia. We investigated whether this treatment changes biochemical parameters and intestinal mucosal barrier function in rats exposed to toxic levels of CO. Groups of ten Sprague–Dawley rats were treated with CO, with hyperbaric oxygen, or with CO followed by hyperbaric oxygen. A fourth group maintained under normal atmospheric conditions served as a control. CO poisoning increased red blood cell distribution width and the amount of alanine aminotransferase, urea nitrogen, and tight junction creatine kinase but decreased the mean corpuscular hemoglobin (Hb). These changes were reversed after hyperbaric oxygen therapy, which increased the number of red blood cells, hematocrit level, total protein, and Hb level. Hyperbaric oxygen therapy also increased tight junction protein 1 expression and reduced toll-like receptor 4 expression in the rat colon. In conclusion, hyperbaric oxygen resulted in an improved oxic condition in CO-poisoned rats and restored energy metabolism by repairing, to some extent, the organs injured by CO. The therapy may also improve the function of the intestinal mucosal barrier. 相似文献
Since the concept of the osmotic microbial fuel cell (OsMFC) was introduced in 2011, it has attracted growing interests for its potential applications in wastewater treatment and energy recovery. However, forward osmosis (FO) membrane fouling resulting in a severe water flux decline remains a main obstacle. Until now, the fouling mechanisms of FO membrane especially the development of biofouling layer in the OsMFC are not yet clear. Here, the fouling behavior of FO membrane in OsMFCs was systematically investigated. The results indicated that a thick fouling layer including biofouling and inorganic fouling was existed on the FO membrane surface. Compared to the inorganic fouling, the biofouling played a more important role in the development of the fouling layer. Further analyses by the confocal laser scanning microscopy (CLSM) implied that the growth of biofouling layer on the FO membrane surface in the OsMFC could be divided into three stages. Initially, microorganisms associated with ß-D-glucopyranose polysaccharides were deposited on the FO membrane surface. After that, the microorganisms grew into a biofilm caused a quick decrease of water flux. Subsequently, some of microorganisms were dead due to lack of nutrient source, in the meantime, polysaccharide and proteins in the biofouling layer were decomposed as nutrient source, thus leading to a slow development of the biofouling layer. Moreover, the microorganisms played a significant role in the formation and development of the biofouling layer, and further studies are needed to mitigate the deposition of microorganisms on FO membrane surfaces in OsMFCs.
