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尿排出量
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  “尿排出量”译为未确定词的双语例句
     Intestinal permeability was assessed by the 24 h urinary recovery of orally gave 99m Tc DTPA.
     测定口服99mTc-DTPA后尿排出量来反映肠道通透性。
短句来源
     It is still fuzzy to interpret the mechanisms of San Jin Capsule's effects of increasing urine secretion and lowering urinal Na+ and Cl-,but in high dose raising urinal K+. 
     三金胶囊增加尿排出量而减少尿Na+、Cl-含量以及大剂量增加尿K+含量的机理尚不清楚
短句来源
     Conclusions:It is viable and safe to supply vitamin C in 500 mg dose a day to surgical patients,and it is superfluous to supply vitamin C in 1 000 mg/day.
     补给维生素 C 10 0 0 mg/ d是过量的 ,血清维生素 C含量饱和 ,2 4h尿排出量明显增加
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  相似匹配句对
     The excreted amount of urinary calcium increase in the severe patients.
     重症患者尿排出量增加 ;
短句来源
     STUDY OF URINARY THIOETHER EXCRETION IN RUBBER INDUSTRY WORKERS
     橡胶生产工人尿硫醚排出量的研究
短句来源
     The blood and urine osmolalities were determined at the same time.
     尿渗透压。
短句来源
     proteinuria(-);
     尿蛋白(-);
短句来源
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  urinary output
Alterations in water intake and urinary output had no effect on biopterin levels related to creatinine.
      
In both groups, the fluid input and urinary output were similar (P>amp;gt; 0.20).
      
In the elderly, magnesium intake tends to be low, intestinal absorption is frequently diminished, and urinary output is often enhanced.
      
In patients with advanced liver disease, decreases in renal blood flow, glomerular filtration rate, and urinary output are frequently observed.
      
The treatment led to significant increases in fluid and Na+ intake and urinary output of fluid and Na+ in sgk1+/+ mice, effects blunted in sgk1-/- mice.
      
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Schizandrol A is one of the active constituents isolated from the ethanol extract of dried fruit of Schizandra chinensis Baill (Fructus Schizandra). It was found to have neuroleptic and anticonvulsive effects in animals. A method of high specificity using TLC for the determination of Schizandrol A in biological, specimens was developed and used in the study of the metabolism of the drug in rats and the distrubution in various areas of rat brain.After oral administration Schizandrol A was found to be readily,...

Schizandrol A is one of the active constituents isolated from the ethanol extract of dried fruit of Schizandra chinensis Baill (Fructus Schizandra). It was found to have neuroleptic and anticonvulsive effects in animals. A method of high specificity using TLC for the determination of Schizandrol A in biological, specimens was developed and used in the study of the metabolism of the drug in rats and the distrubution in various areas of rat brain.After oral administration Schizandrol A was found to be readily, absorbed from the gastro-intestinal tract (t_(1/2)=58 min). The bloodlevel of Schizandrol A following iv injection showed a biphasic decline as a function of time, the distribution phase and the elimination phase. The pharmacokinetic parameters were as follows:t_(1/2α)=1.44 min, t_(1/2β)=42.14 min, K_(10)=0.08/min, K_(12)=0.32/min, K_(21)=0.10/min, V_c=0.75 L/kg, V_d=3.60 L/kg. Schizandrol A was detectable in urine one hour after oral administration About 0.35% of the dose was recovered from urine within 26 hours. Five minutes after iv injection highest levels of Schizandrol A was found in the lung, moderate in liver, heart, brain and kidneys, and low in ileum and spleen. These results indicate that Schizandrol A was distributed widely in the body and eliminated rapidly.The distribution of Schizandrol A in various areas of the brain was as follows:highest levels was found in hypothalamus, striatum and hippocampus, moderate indiencephalon and lower stem, and low in cerebral Cortex and cerebelum. The different levels in various regions of the brain might be relevant to the neuroleptic and cataleptic effects of Schizandrol A.

五味子醇甲为五味子乙醇提取物中有效成分之一,具有明显中枢安定作用,本文用薄层紫外扫描方法测定醇甲在大鼠及小鼠体内的吸收、分布、排泄及脑内分布。 大鼠口服醇甲后,胃肠吸收快,静注后血药浓度呈开放二室模型。组织分布以肺浓度最高,其次为肝、心、脑、肾、肠、脾及肠最低。脑内分布以下丘脑、纹体、海马浓度最高,其次为低位脑干及间脑,大脑皮层和小脑浓度较低。静注后由尿排出量很少。醇甲自整体小鼠的消失快。结果表明醇甲自胃肠道吸收快而完全,代谢及排泄较快,组织分布广。各脑区药物浓度的差别可能与其中枢作用有关。

In this paper is reported the investigation of the distribution and fate of 14C-pec tin from pomelo's shell in mice as well as that of 14C-dextran in comparison by means of the tracer experiment.The plasma concentration-time profile following i. v.injection of a single dose of 14C-pectin was described by a two compartment open pharmacoki-netic model. Distribution of 14C-pectin proceeded rapidly with half-life 9 minutes and elimination half-life was about 3 hours.The radioactive concentration of 14C-pectin was...

In this paper is reported the investigation of the distribution and fate of 14C-pec tin from pomelo's shell in mice as well as that of 14C-dextran in comparison by means of the tracer experiment.The plasma concentration-time profile following i. v.injection of a single dose of 14C-pectin was described by a two compartment open pharmacoki-netic model. Distribution of 14C-pectin proceeded rapidly with half-life 9 minutes and elimination half-life was about 3 hours.The radioactive concentration of 14C-pectin was higher in the kidneys than in the other tissues during 30 minutes after injection, whereas the liver held the highest concentration of radioactivity as compared with other organs at 1 hour after administration of 14C-pectin.In the first 8 hours 78% of the dose of drug was excreted in the urine of mice. The approximate 94.3% was eliminated from the feces and urine within 72 hours following the injection of single dose. The paper chromatography revealed that 82% of parent compound in the liver and urine remained unchanged.

本文应用放射性同位素示踪法,对LCR种小鼠静注~(14)C-柚皮果胶进行了药物动力学、组织分布、排泄和药物代谢的研究,并与~(14)C-右旋糖酐做了对比观察。血浆药物浓度的消除属于一级动力学的动态变化,符合开放形二室模型。其分布相半衰期较短为9分钟,排除相半衰期大约为3小时。静脉注射后30分钟内肾脏的药物浓度较高,而给药1小时后肝脏药物浓度较高。静注后8小时内从尿的排出量为给药量的78%,给药后72小时尿和粪的总排出量为94.3%。应用放射性纸层分析法,显示肝和尿中放射性物质的性质约有82%是原形药物。

七条犬应用左心辅助装置进行辅助循环,犬平均存活时间为17~45.5(24.5)小时,血泵输出量为883mL/分。死亡原因:室颤3例,出血及肺部并发症4例。左心辅助装置进行辅助循环的血液动力学效应是,心率减慢,心输出量和尿排出量增加,主动脉收缩压、左室收缩压和左室舒张末压降低。主动脉舒张压升高和冠伏动脉灌注增强。实验室检查:血浆游离血红蛋白逐渐增加而血浆纤维蛋白含量逐渐减少。尿素氮、CO_2结合率和血浆钾、钠含量均维持在正常范围。尸解显示在心肌、肝、肾、脾、肺及脑组织中可见局部出血、间质水肿及细胞坏死。

 
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