The aim of the current study was to gain a better understanding of the changes in soil microbial biomass and basal respiration dynamics in the vicinity of the bean caper （Zygophyllura duraosura） perennial desert shr...The aim of the current study was to gain a better understanding of the changes in soil microbial biomass and basal respiration dynamics in the vicinity of the bean caper （Zygophyllura duraosura） perennial desert shrub and the inter-shrub sites. Microbial biomasses as well as basal respiration were found to be significantly greater in the soil samples taken beneath the Z. duraosura shrubs than from the inter-shrub sampling sites, with no differences between the two sampling layers （0-10 and 10-20 cm） throughout the study period. However, seasonal changes were observed due to autumn dew formation, which significantly affected microbial biomass and basal respiration in the upper-layer inter-shrub locations. The calculated metabolic coefficient （qCO2） revealed significant differences between the two sampling sites as well as between the two soil layers, elucidating the abiotic effect between the sites throughout the study period. The substrate availability index was found to significantly demonstrate the differences between the two sites, elucidating the significant contribution of Z. duraosura in food source availability and in moderating harsh abiotic components. The importance of basal microbial parameters and the derived indices as tools demonstrated the importance and need for basic knowledge in understanding plant-soil interactions determined by an unpredictable and harsh desert environment.展开更多
OBJECTIVE:To investigate the effect of black catechu(BC) on the pharmacokinetics of theophylline(CYP1A2 substrate,with narrow therapeutic index)in rabbits.METHODS:In the present investigation the effect of BC on the p...OBJECTIVE:To investigate the effect of black catechu(BC) on the pharmacokinetics of theophylline(CYP1A2 substrate,with narrow therapeutic index)in rabbits.METHODS:In the present investigation the effect of BC on the pharmacokinetics of theophylline,a CYP1A2 substrate was determined.In the study,BC(264 mg/kg,p.o.) or saline(control group) was given to rabbits for 7 consecutive days and on the 8^(th)day theophylline(16 mg/kg) was administered orally one hour after BC or saline treatment.Blood samples were withdrawn at different time intervals(0.5,1,1.5,2,3,4,6,8,12,24 and 36 h) from the marginal ear vein.RESULTS:The pretreatment of rabbits with BC resulted in a significant increase in maximum blood concentration,time of peak concentration and area under the concentration time profile curve until last observation which was about 41.32%,35.71%and 15.03%,respectively.While decreases in clearance,volume of distribution,and half-life were observed.It is suggested that BC pretreatment decreases the CYP1 A metabolic activity leading to increase in bioavailability and decrease in oral clearance of theophylline,which may be due to inhibition of CYP1 A.CONCLUSION:BC can significantly alter theophylline pharmacokinetics in vivo possibly due to inhibition of CYP1 A and P-glycoprotein activity.Based on these results,precaution should be exercised when administering BC with CYP1 A substrate.展开更多
文摘The aim of the current study was to gain a better understanding of the changes in soil microbial biomass and basal respiration dynamics in the vicinity of the bean caper （Zygophyllura duraosura） perennial desert shrub and the inter-shrub sites. Microbial biomasses as well as basal respiration were found to be significantly greater in the soil samples taken beneath the Z. duraosura shrubs than from the inter-shrub sampling sites, with no differences between the two sampling layers （0-10 and 10-20 cm） throughout the study period. However, seasonal changes were observed due to autumn dew formation, which significantly affected microbial biomass and basal respiration in the upper-layer inter-shrub locations. The calculated metabolic coefficient （qCO2） revealed significant differences between the two sampling sites as well as between the two soil layers, elucidating the abiotic effect between the sites throughout the study period. The substrate availability index was found to significantly demonstrate the differences between the two sites, elucidating the significant contribution of Z. duraosura in food source availability and in moderating harsh abiotic components. The importance of basal microbial parameters and the derived indices as tools demonstrated the importance and need for basic knowledge in understanding plant-soil interactions determined by an unpredictable and harsh desert environment.
基金the Deanship of Scientific Research at King Saud University for funding this research group,No. RG-1435-041
文摘OBJECTIVE:To investigate the effect of black catechu(BC) on the pharmacokinetics of theophylline(CYP1A2 substrate,with narrow therapeutic index)in rabbits.METHODS:In the present investigation the effect of BC on the pharmacokinetics of theophylline,a CYP1A2 substrate was determined.In the study,BC(264 mg/kg,p.o.) or saline(control group) was given to rabbits for 7 consecutive days and on the 8^(th)day theophylline(16 mg/kg) was administered orally one hour after BC or saline treatment.Blood samples were withdrawn at different time intervals(0.5,1,1.5,2,3,4,6,8,12,24 and 36 h) from the marginal ear vein.RESULTS:The pretreatment of rabbits with BC resulted in a significant increase in maximum blood concentration,time of peak concentration and area under the concentration time profile curve until last observation which was about 41.32%,35.71%and 15.03%,respectively.While decreases in clearance,volume of distribution,and half-life were observed.It is suggested that BC pretreatment decreases the CYP1 A metabolic activity leading to increase in bioavailability and decrease in oral clearance of theophylline,which may be due to inhibition of CYP1 A.CONCLUSION:BC can significantly alter theophylline pharmacokinetics in vivo possibly due to inhibition of CYP1 A and P-glycoprotein activity.Based on these results,precaution should be exercised when administering BC with CYP1 A substrate.
