ABSTRACT
Objective@#To observe the preventive effect of alkaline drinking water on hyperuricemia in mice. @*Methods@#Sixty male SPF Kunming mice were randomly divided into six groups: pH 7.3, pH 8.0, pH 9.3 intervention groups, in which the mice were given water with pH values of 7.3±0.5, 8.0±0.5 and 9.3±0.6, respectively; the control group, model group and positive drug group ( with 2 g/L allopurinol ) were given double distilled water. Except for the control group, the mice in each group were given yeast by gavage (1.5 g/mL) for 13 days. On the 14th day, the mice were injected with 300 mg/kg potassium oxyzinate by intraperitoneal injection, and then fasted for 1 day. On the 16th day, serum uric acid, creatinine and urea nitrogen were detected, and renal tissues were stained to observe the morphology.The expression levels of neutrophil gelatinase-associated lipocalin ( NGAL ), tissue inhibitor of metalloproteinase 1( TIMP1 ), organic anion transporter 1 ( OAT1 ) and urate transporter 1 ( URAL-1 ) in renal tissues were determined bywestern blotting. The mRNA expression levels of URAL-1 and OAT1 were detected by real-time fluorescent quantita⁃tive polymerase chain reaction.@*Results@#The level of serum uric acid was higher in the model group than in the control group and in the pH 9.3 intervention group (both P<0.05). The number and area of renal tubular lesions were less in the pH 9.3 intervention group than in the model group (all P<0.05). The relative expression levels of NGAL and URAT-1 proteins were lower in the pH 9.3 intervention group than in the model group, and the relative expression level of OAT1 protein was higher in the pH 9.3 intervention group than in the model group ( all P<0.05). The relativeexpression level of URAT-1 mRNA was lower in the pH 9.3 intervention group than in the model group, and the rela⁃tive expression level of OAT1 mRNA was higher in the pH 9.3 intervention group than in the model group ( all P<0.05 ).@*Conclusion@#Alkaline drinking water with pH value of 9.3±0.6 can effectively prevent hyperuricemia and acute kidney injury in mice.
ABSTRACT
Background: Zamzam water is naturally alkaline and rich in a variety of minerals which may represent a powerful tool for cancer therapy. In this research, the cytotoxic effects of Zamzam water were investigated in human lung cancer (A549) cell line and compared with human skin fibroblasts (HSF). Methods: Two different preparations of Zamzam water were used: Z1, with pH adjusted to 7.2 and Z2, with no pH adjustment. The effects of both treatments on the morphology of the A549 and HSF cell lines were investigated. The cell viability of HSF and A549 cells was identified by the MTT assay and trypan blue exclusion. Detection of apoptotic cells and cell cycle analyses were determined using flow cytometry. Moreover, reactive oxygen species (ROS) were measured for both cell lines. Results: Both Zamzam water treatments, Z1 and Z2 showed reductions in the cell viability of A549 cells. Cell death occurred via necrosis among cells treated with Z2. Cell cycle arrest occurred in the G0/G1 phases for cells treated with Z2. Cellular and mitochondrial ROS productions were not affected by either treatment. Conclusion: Our findings indicate that Zamzam water might have potential therapeutic efficacy for lung cancer.
ABSTRACT
OBJECTIVE:To optimize extraction technology of polysaccharides from Stemona tuberosa so as to increase the ex-traction rate and efficiency. METHODS:Anthrone-sulfuric acid method was used for detection. With water and alkaline water (NaOH solution)as the solvent respectively,the effects of decocting method,ultrasound method and microwave method on the ex-traction rate of crude polysaccharide were observed respectively. By carrying out single factor and orthogonal tests,with the extrac-tion rate of crude polysaccharide as the index,the effects of the amount of water,NaOH solution concentration,extraction tempera-ture and extraction time on the extraction of crude polysaccharide by alkaline water ultrasound method were observed to optimize the technology parameters,and verification test was conducted. RESULTS:The alkaline water ultrasound method is superior to oth-er extraction methods,where the optimal technology parameters were as follows as 0.3 mol/L NaOH aqueous solution 30 times as much as the amount of crud drug,ultrasonic processing for 70 min at 50 ℃. The verification tests showed that the average extrac-tion rate of crude polysaccharide was 25.76%(RSD=3.51%,n=6). CONCLUSIONS:The optimal alkaline water ultrasound method can better extract crude polysaccharide from S. tuberosa.
ABSTRACT
The objective of this study was to investigate the effects of exposure to low water hardness (0, 25 and 50mg CaCO3L-1) into the 6.0-8.0 pH range to silver catfish juveniles (Rhamdia quelen) survival and growth after 32 days. Juveniles kept at zero water hardness presented higher mortality at pH 7.0 and 8.0 than those submitted to other treatments. Weight of juveniles exposed to pH 6.0 and zero water hardness was significantly higher than those kept at the same water hardness and other pH. Survival and growth of juveniles exposed to 25 and 50mg CaCO3 L-1 was not affected in the 6.0-8.0 pH range. Therefore, the best water hardness for silver catfish juveniles growth is 25-50mg CaCO3 L-1 and at low water hardness (next zero) pH must be reduced.
O objetivo deste estudo foi investigar os efeitos da exposição em baixas durezas da água (0; 25 e 50mg CaCO3 L-1) na faixa de pH 6,0-8,0 no crescimento e na sobrevivência de juvenis de jundiás (Rhamdia quelen). Os juvenis foram expostos aos tratamentos durante 32 dias. Os indivíduos mantidos em dureza zero da água apresentaram maior mortalidade em pH 7,0 e 8,0 do que aqueles submetidos aos outros tratamentos. O peso dos juvenis expostos ao pH 6,0 com zero dureza da água foram significativamente maiores do que aqueles mantidos na mesma dureza e em outras faixas de pH. A sobrevivência e o crescimento dos indivíduos expostos em 25 e 50mg CaCO3L-1 não foi afetado na faixa de pH 6,0-8,0. Portanto, a melhor dureza da água para o crescimento e de juvenis de jundiá é 25-50mg CaCO3 L-1 e em baixa dureza da água (próxima a zero) o pH deve ser reduzido.