The effects of environmental Na+/K+ ratio on the gill ion-transport enzyme activity,plasma osmolality and growth of Cynoglossus semilaevis juveniles were investigated. The results showed that,plasma osmolality was sim...The effects of environmental Na+/K+ ratio on the gill ion-transport enzyme activity,plasma osmolality and growth of Cynoglossus semilaevis juveniles were investigated. The results showed that,plasma osmolality was similar among flounder adapted to different Na+/K+ ratios of saline groundwaters (P>0.05),while the growth,gill Na+,K+-ATPase and HCO3--ATPase activities were affected by Na+/K+ ratio significantly (P<0.05). The gill Na+,K+-ATPase activity reached its maximum on day 3,then decreased gradually from day 3 to day 9 and remained constant from day 9 to day 15. The peak values of gill Na+,K+-ATPase activity were detected on day 3 for all Na+/K+ ratios of saline groundwaters,then the enzyme activities descended,and on day 9 the enzyme activi-ties achieved steady state,and the gill HCO3--ATPase activity increased rapidly and achieved steady state after one day. During steady state,the gill Na+,K+-ATPase and HCO3--ATPase activity of Na+/K+ ratios 20 and 40 treatments were significantly higher than those in the control group (Na+/K+ ratio 27.5),while there were no significant differences between the Na+/K+ ratio 30 treatment and the control group; the gill Na+,K+-ATPase activity of Na+/K+ ratio 20 and 40 treatments were significantly higher than that for ratio 30 treatment,but there were no significant differences of gill HCO3--ATPase activity among these treatments. At the end of the 15-day experiment,the weight gain (%) and specific growth rate (SGR) of flounders maintained in seawater were significantly higher than those in groundwaters; significant differences also occurred among the treatments; Na+/K+ ratio 30 treatment had the highest values (33.7% and 1.94 respectively),which were significantly higher than those under Na+/K+ ratios 20 and 40 treatments. There-fore,for the saline groundwater used in this experiment,it is suggested that the Na+/K+ ratio be adjusted to approximately 30,i.e.,as close to that of natural seawater as possible in the culture of flounder.展开更多
For preparing fluorinated quinolone antibiotic medicine locally used in stomatology, simultaneous determination of norfloxacin, ciprofloxacin, and enoxacin was carried out by multiphase ion chromatography with fluores...For preparing fluorinated quinolone antibiotic medicine locally used in stomatology, simultaneous determination of norfloxacin, ciprofloxacin, and enoxacin was carried out by multiphase ion chromatography with fluorescence detection. Quinolone antibiotics were separated by Dionex OmniPac PAX-500 column with an eluent of 15 mmol/L H2SO4 and 35% methanol （v/v） at a flow-rate of 1.0 ml/min and detected with fluorescence with excitation and emission wave lengths of 347 ran and 420 ran respectively. The detection limits （S/N=3） of norfloxacin, ciprofloxacin and enoxacin were 50, 105 and 80 ng/ml respectively. The relative standard deviations of retention time, peak area and peak height were less than 1.1% and good linear relationship resulted. The developed method was applied to pharmaceutical formulations and biological fluids.展开更多
AIM:To investigate the effect of chloride intracellular channel 1(CLIC1) on the cell proliferation,apoptosis,migration and invasion of gastric cancer cells.METHODS:CLIC1 expression was evaluated in human gastric cance...AIM:To investigate the effect of chloride intracellular channel 1(CLIC1) on the cell proliferation,apoptosis,migration and invasion of gastric cancer cells.METHODS:CLIC1 expression was evaluated in human gastric cancer cell lines SGC-7901 and MGC-803 by real time polymerase chain reaction(RT-PCR).Four segments of small interference RNA(siRNA) targeting CLIC1 mRNA and a no-sense control segment were designed by bioinformatics technology.CLIC1 siRNA was selected using Lipofectamine 2000 and transfected transiently into human gastric cancer SGC-7901 and MGC-803 cells.The transfected efficiency was observed under fluorescence microscope.After transfection,mRNA expression of CLIC1 was detected with RT-PCR and Western blotting was used to detect the protein expression.Proliferation was examined by methyl thiazolyl tetrazolium and apoptosis was detected with flow cytometry.Polycarbonate membrane transwell chamber and Matrigel were used for the detection of the changes of invasion and migration of the two cell lines.RESULTS:In gastric cancer cell lines SGC-7901 and MGC-803,CLIC1 was obviously expressed and CLIC1 siRNA could effectively suppress the expression of CLIC1 protein and mRNA.Proliferation of cells transfected with CLIC1 siRNA3 was enhanced notably,and the highest proliferation rate was 23.3%(P = 0.002) in SGC-7901 and 35.55%(P = 0.001) in MGC-803 cells at 48 h.The G2/M phase proportion increased,while G0/G1 and S phase proportions decreased.The apoptotic rate of the CLIC1 siRNA3 group obviously decreased in both SGC-7901 cells(62.24%,P = 0.000) and MGC-803 cells(52.67%,P = 0.004).Down-regulation of CLIC1 led to the inhibition of invasion and migration by 54.31%(P = 0.000) and 33.62%(P = 0.001) in SGC-7901 and 40.74%(P = 0.000) and 29.26%(P = 0.002) in MGC-803.However,there was no significant difference between the mock group cells and the negative control group cells.展开更多
基金the Agricultural Science and Technology Achievement Transfer Project of Tianjin City of China (Transfer of the Large-scale health culture technology of fish and shrimp)the Science and Technology Program of Shengli Oil Field Administration Bureau (The exploring study on the culture technology of fish and shrimp using saline groundwaters)
文摘The effects of environmental Na+/K+ ratio on the gill ion-transport enzyme activity,plasma osmolality and growth of Cynoglossus semilaevis juveniles were investigated. The results showed that,plasma osmolality was similar among flounder adapted to different Na+/K+ ratios of saline groundwaters (P>0.05),while the growth,gill Na+,K+-ATPase and HCO3--ATPase activities were affected by Na+/K+ ratio significantly (P<0.05). The gill Na+,K+-ATPase activity reached its maximum on day 3,then decreased gradually from day 3 to day 9 and remained constant from day 9 to day 15. The peak values of gill Na+,K+-ATPase activity were detected on day 3 for all Na+/K+ ratios of saline groundwaters,then the enzyme activities descended,and on day 9 the enzyme activi-ties achieved steady state,and the gill HCO3--ATPase activity increased rapidly and achieved steady state after one day. During steady state,the gill Na+,K+-ATPase and HCO3--ATPase activity of Na+/K+ ratios 20 and 40 treatments were significantly higher than those in the control group (Na+/K+ ratio 27.5),while there were no significant differences between the Na+/K+ ratio 30 treatment and the control group; the gill Na+,K+-ATPase activity of Na+/K+ ratio 20 and 40 treatments were significantly higher than that for ratio 30 treatment,but there were no significant differences of gill HCO3--ATPase activity among these treatments. At the end of the 15-day experiment,the weight gain (%) and specific growth rate (SGR) of flounders maintained in seawater were significantly higher than those in groundwaters; significant differences also occurred among the treatments; Na+/K+ ratio 30 treatment had the highest values (33.7% and 1.94 respectively),which were significantly higher than those under Na+/K+ ratios 20 and 40 treatments. There-fore,for the saline groundwater used in this experiment,it is suggested that the Na+/K+ ratio be adjusted to approximately 30,i.e.,as close to that of natural seawater as possible in the culture of flounder.
基金Project supported by the National Natural Science Foundation of China (Nos.20375035 and 20527005)the Natural Science Foundation of Zhejiang Province (No.Z404105), China
文摘For preparing fluorinated quinolone antibiotic medicine locally used in stomatology, simultaneous determination of norfloxacin, ciprofloxacin, and enoxacin was carried out by multiphase ion chromatography with fluorescence detection. Quinolone antibiotics were separated by Dionex OmniPac PAX-500 column with an eluent of 15 mmol/L H2SO4 and 35% methanol （v/v） at a flow-rate of 1.0 ml/min and detected with fluorescence with excitation and emission wave lengths of 347 ran and 420 ran respectively. The detection limits （S/N=3） of norfloxacin, ciprofloxacin and enoxacin were 50, 105 and 80 ng/ml respectively. The relative standard deviations of retention time, peak area and peak height were less than 1.1% and good linear relationship resulted. The developed method was applied to pharmaceutical formulations and biological fluids.
基金Supported by The National Natural Science Foundation of China,No.30560151the Key Research Project of Guangxi Municipal Health Bureau,No.200824+1 种基金the Research Project of Guangxi Educational Department,No.201012MS062 and No. 2011105981002M204the Natural Science Foundation of Guangxi,No.0832113
文摘AIM:To investigate the effect of chloride intracellular channel 1(CLIC1) on the cell proliferation,apoptosis,migration and invasion of gastric cancer cells.METHODS:CLIC1 expression was evaluated in human gastric cancer cell lines SGC-7901 and MGC-803 by real time polymerase chain reaction(RT-PCR).Four segments of small interference RNA(siRNA) targeting CLIC1 mRNA and a no-sense control segment were designed by bioinformatics technology.CLIC1 siRNA was selected using Lipofectamine 2000 and transfected transiently into human gastric cancer SGC-7901 and MGC-803 cells.The transfected efficiency was observed under fluorescence microscope.After transfection,mRNA expression of CLIC1 was detected with RT-PCR and Western blotting was used to detect the protein expression.Proliferation was examined by methyl thiazolyl tetrazolium and apoptosis was detected with flow cytometry.Polycarbonate membrane transwell chamber and Matrigel were used for the detection of the changes of invasion and migration of the two cell lines.RESULTS:In gastric cancer cell lines SGC-7901 and MGC-803,CLIC1 was obviously expressed and CLIC1 siRNA could effectively suppress the expression of CLIC1 protein and mRNA.Proliferation of cells transfected with CLIC1 siRNA3 was enhanced notably,and the highest proliferation rate was 23.3%(P = 0.002) in SGC-7901 and 35.55%(P = 0.001) in MGC-803 cells at 48 h.The G2/M phase proportion increased,while G0/G1 and S phase proportions decreased.The apoptotic rate of the CLIC1 siRNA3 group obviously decreased in both SGC-7901 cells(62.24%,P = 0.000) and MGC-803 cells(52.67%,P = 0.004).Down-regulation of CLIC1 led to the inhibition of invasion and migration by 54.31%(P = 0.000) and 33.62%(P = 0.001) in SGC-7901 and 40.74%(P = 0.000) and 29.26%(P = 0.002) in MGC-803.However,there was no significant difference between the mock group cells and the negative control group cells.
