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胃肠吸收
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  gastrointestinal absorbent
     The study on the mechanism of Yunpi method on improving gastrointestinal motility and repairing gastrointestinal absorbent cells' ultrastructure of anorexia animal model
     运脾法改善厌食动物模型胃肠动力及胃肠吸收细胞超微结构的机理研究
短句来源
     According to the theory "For invigorating spleen, it抯 better to activate it than to tonify it" which was put forward by professor Jiang yuren, we have done some experiments and probed the mechenism of Yunpi method on improving gastrointestinal motility and repairing gastrointestinal absorbent cells' ultrastructure of the anorexia animal model.
     我们在江育仁教授提出的“脾健不在补贵在运”理论指导下,以运脾法为主,通过实验研究,探讨运脾法改善厌食症模型胃肠动力及胃肠吸收细胞超微结构的作用机理。
短句来源
     Lastly,it can repair the gastrointestinal absorbent cells' ultrastructure of the animal model.
     ④恢复厌食症模型的胃肠吸收细胞超微结构。
短句来源
  “胃肠吸收”译为未确定词的双语例句
     Gastroenteric Absorptive Kinetic Study on Strychine in Jiufensan
     九分散中士的宁的胃肠吸收动力学研究
短句来源
     3 Shuang gu yi tong acupuncture therapy could increase ALP, Ca in blood and decrease P in blood, Ca/Cr in urine to regulate bone metabolism.
     4.“双固一通”针法能改善Ca、P代谢,其作用机制可能是通过针刺的整体调节,增加胃肠吸收功能,促进Ca、P等物质的代谢,促进骨形成。 关健词PMO血Ca血P临床研究“双固一通”针法骨密度EZ IL一6血ALP尿Ca/Cr
短句来源
     The radioactivity in organs was eliminated slowly. After iv 3H-triptolide (the highest dose) to mice and rats, the area under the curve (AUC) was increased, the clearance (Cl) was decreased and the elimination half-life (tl/2β) was prolonged. The results indicated that the triptolide can be appeared nonlinear pharmacokinetics.
     小鼠的胃肠吸收较大鼠快,T peak分别为0.687、1.037h,体内消除较缓慢,在高剂量下可见AUC增大、C1减少及t1/2β延长,提示临床上在高剂量应用时可能出现的非线性动力学性质。
短句来源
     The lowering of urine D-xylose absorption rate and haemoglobin compared with those of normal group. P<0.001.The rats' microvilli of gastric mucosa were dam- aged under scanning electron microscope.
     其脾虚表现符合全国统一标准,代表胃肠吸收功能的尿 D-木糖吸收率及血红蛋白下降(与正常对照鼠比,P<0.001),扫描电镜下鼠胃粘膜可见微绒毛损伤;
短句来源
     It appeared that the absorption of the bismuth is less in the gastrointestinal tract and its bioavailability is lower.
     Cmax为0.10,0.24和0.33μmol/L.用静脉注射和灌胃的中剂量AUC统计铋的生物利用度为5.22%.结果提示,铋胃肠吸收极少,生物利用度低,大部分从胃肠道排出体外.
短句来源
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  相似匹配句对
     Gastrointestinal lnterstitialoma:A Tumor Originate from Gastrointestinal Pacemaker Cell
     胃肠间质瘤
短句来源
     Gastroenteric Absorptive Kinetic Study on Strychine in Jiufensan
     九分散中士的宁的胃肠吸收动力学研究
短句来源
     K uptake by spring maize is significantly improved by potassium fertilizer and established the dynamic model of N.
     K的吸收。 建立了N.
短句来源
     c)The efficiency of absorbing.
     c)吸收效率;
短句来源
     Lastly,it can repair the gastrointestinal absorbent cells' ultrastructure of the animal model.
     ④恢复厌食症模型的胃肠吸收细胞超微结构。
短句来源
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  gastrointestinal absorption
The three last mentioned are prodrugs which upon gastrointestinal absorption are rapidly split to yield circulating ampicillin.
      
Gastrointestinal absorption of Me203Hg was not influenced by the Se status of the animals.
      
Increased gastrointestinal absorption and urinary excretion of zinc has been confirmed in experimental and clinical studies on primary arterial hypertension as a result from changes of intracellular and extracellular zinc content.
      
The drugs must be given on an empty stomach because food and beverages interfere with gastrointestinal absorption.
      
Gastrointestinal absorption studies in cardiac cachexia
      
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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。

The pharmacokinetics of [~3H]-benzothia-zole-Rifamycin was studied in mice and rats. Absorption of [~3H]-benzothiazole-Rifa-mycin from the gastrointestinal tract of

本文研究了我国创制的苯噻唑力复霉素在小白鼠和大白鼠体内的药代动力学。[~3H]-苯噻唑力复霉素自大白鼠和小白鼠的胃肠吸收较快,但吸收程度差。小白鼠和大白鼠口服[~3H]-苯噻唑力复霉素后,分别于1.8小时和3.5小时血中放射性达高峰。血浆药-时曲线分快、慢两个时相,按开放二室模型计算动力学参数。小白鼠:t_(1/2)α=0.86/小时,t_(1/2)β=24.45小时,t_(1/2) K_a=0.40小时,K_(21)=0.16小时~(-1),K_(12)=0.55小时~(-1),t_(max)=1.77小时,C_(max)=8148cpm/0.1ml;大白鼠:t_(1/2)α=2.48小时,t_(1/2)β=30.32/小时,t_(1/2)K_a=0.76小时,K_(21)=0.16小时~(-1),K_(12)=0.11小时~(-1),t_(max)=3.55小时,C_(max)=10962cpm/0.1ml。可见,小白鼠对[~3H]-苯噻唑力复霉素的胃肠吸收和体内分布均较大白鼠为快。 [~3H]-苯噻唑力复霉素广泛分布于大白鼠和小白鼠的各组织器官。肝中放射性最高,其它依次为肾、肺、...

本文研究了我国创制的苯噻唑力复霉素在小白鼠和大白鼠体内的药代动力学。[~3H]-苯噻唑力复霉素自大白鼠和小白鼠的胃肠吸收较快,但吸收程度差。小白鼠和大白鼠口服[~3H]-苯噻唑力复霉素后,分别于1.8小时和3.5小时血中放射性达高峰。血浆药-时曲线分快、慢两个时相,按开放二室模型计算动力学参数。小白鼠:t_(1/2)α=0.86/小时,t_(1/2)β=24.45小时,t_(1/2) K_a=0.40小时,K_(21)=0.16小时~(-1),K_(12)=0.55小时~(-1),t_(max)=1.77小时,C_(max)=8148cpm/0.1ml;大白鼠:t_(1/2)α=2.48小时,t_(1/2)β=30.32/小时,t_(1/2)K_a=0.76小时,K_(21)=0.16小时~(-1),K_(12)=0.11小时~(-1),t_(max)=3.55小时,C_(max)=10962cpm/0.1ml。可见,小白鼠对[~3H]-苯噻唑力复霉素的胃肠吸收和体内分布均较大白鼠为快。 [~3H]-苯噻唑力复霉素广泛分布于大白鼠和小白鼠的各组织器官。肝中放射性最高,其它依次为肾、肺、脾、心、肌、脑。整体放射自显影结果与液闪法一致。 放射性主要自粪和胆汁排泄,原也排泄部分放射性。给药后7天,自粪和尿分别排出剂量的65.49%和30.85%;给药后24小时,自胆汁排出剂量的19.34%。苯噻唑力复霉素的血浆蛋白结合率为81.36%。

Triptolide extracted from Tripterygium wilfordii Hook.f. possesses antituinor, anti-inflammatory and immuncsupression activity. After singe dose intragastric (ig) and Three doses intravenous (iv) administration of H-triptaiide to rats and mice, the declie of radioactivity in the plasma was shown to be two-crmpartment mcdel and three-compartment model, respectively. The peak radioactivity level in plasn:a for mice and rats was 0.69 h and 1.04 h, respectively. The radioactivity in organs was eliminated slowly....

Triptolide extracted from Tripterygium wilfordii Hook.f. possesses antituinor, anti-inflammatory and immuncsupression activity. After singe dose intragastric (ig) and Three doses intravenous (iv) administration of H-triptaiide to rats and mice, the declie of radioactivity in the plasma was shown to be two-crmpartment mcdel and three-compartment model, respectively. The peak radioactivity level in plasn:a for mice and rats was 0.69 h and 1.04 h, respectively. The radioactivity in organs was eliminated slowly. After iv 3H-triptolide (the highest dose) to mice and rats, the area under the curve (AUC) was increased, the clearance (Cl) was decreased and the elimination half-life (tl/2β) was prolonged. The results indicated that the triptolide can be appeared nonlinear pharmacokinetics.

经小鼠、大鼠ig和iv高、中、低三种剂量的动力学研究结果表明:ig后的药一时曲线为开放二室模型;iv为开放三室模型。小鼠的胃肠吸收较大鼠快,T peak分别为0.687、1.037h,体内消除较缓慢,在高剂量下可见AUC增大、C1减少及t1/2β延长,提示临床上在高剂量应用时可能出现的非线性动力学性质。

 
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