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   不动时间 的翻译结果: 查询用时:0.458秒
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不动时间
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  immobility time
     Results:The model rats showed significantly lower body weight(429±45/494±37,P<0.01),sucrose consumption(8.3±3.3/14.4±2.7,P<0.01)and longer immobility time in forced swimming test(96±10/37±9).
     结果:应激5周后,与正常对照组相比模型组大鼠体重降低(429±45/494±37,P<0.01),糖水消耗量降低(8.3±3.3/14.4±2.7,P<0.01),强迫游泳的不动时间延长(96±10/37±9,P<0.01)。
短句来源
     Immobility time in forced swimming of the 3 dosage groups were also shortened(63±8,66±10,26±8,41±11)compared to the model group(96±10).
     强迫游泳不动时间较模型组大鼠也缩短(63±8、66±10、26±8、41±11/96±10,z=-2.02、-3.52、-3.03,P<0.05或P<0.01)。
短句来源
     The results indicated that microinjection of GABA into OFC could significantly shorten rats' swimming immobility time (n=8, P<0.05), which could be blocked by BM (n=6, P<0.05).
     结果表明:在OFC微量注射GABA能显著缩短大鼠游泳的不动时间(n=8,P<0.05),且这一效应能被BM阻断(n=6,P<0.05).
短句来源
     The high dosage can also reduce the immobility time of tail-suspension mice with the rate of 29.58%(P<0.01).
     高剂量能使悬尾抑郁症模型小鼠不动时间显著缩短,缩短率为29.58%(P<0.01);
短句来源
     Results BCPT 160,80,40,20,10 mg/kg shortened the immobility time in forced swimming mice in dose-dependend and time-dependend manner. BCPT 40,20 mg/kg shortened the immobility time in tail suspension mice.
     结果BCPT160、80、40、20、10mg/kg能缩短强迫游泳小鼠的不动时间,并呈现一定的量效、时效关系,BCPT40、20mg/kg能缩短悬尾小鼠的不动时间
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  “不动时间”译为未确定词的双语例句
     HPE also significantly shortened motionless time of the rat forced swimming test from 140.4±14.3 to 117.0±13.5,105.6±10.3,97.2±38.5s(P<0.01) at the doses of 0.128 6,0.514 3 and 1.028 6g·kg -1 in a dosedependent manner.
     HPE能剂量依赖性的使大鼠强迫游泳的不动时间缩短 ,在剂量为 0 .12 86、0 .5 14 3、1.0 2 86g·kg-1的不动时间由 14 0 .4± 14 .3s分别降低为 117.0±13.5、10 5 .6± 10 .3、97.2± 38.5s(P <0 .0 1)。
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     and at the 14th day′s test,SSD reduced IT significantly for both dose of 75 mg/kg and 125 mg/kg(P<0.05);
     第14天测试75 mg/kg组和125 mg/kg组与对照组相比能够显著缩短不动时间(P<0.05);
短句来源
     After 18 days′ injecting drug,in comparion with the control group,SSD reduced IT significantly for dose of 75 mg/kg(P<0.05) and 100 mg/kg(P<0.01),and the positive-control group that injected fluoxetine reduced IT significantly(P<0.05) for dose of 10 mg/kg.
     连续给药18 d后75 mg/kg组和100 mg/kg组与对照组相比分为显著(P<0.05)和极显著缩短不动时间(P<0.01);
短句来源
     5~20mg· kg-1 ig moclobemide prevented dose-dependently blepharoptosis induced by reserpine(2.8mg·kg-1, sc) in rat. 5 ̄25mg·kg-1(ig)moclobemide significantly decreased the duration of immobility in" dispair" test in mouse.
     吗氯贝胺5、10、20mg·kg-1(ig)可显著对抗利血平(2.8mg·kg-1,sc)引起的大鼠眼睑下垂,其抑制率分别为60%,80%与90%。 在小鼠获得性“绝望”实验中,吗氯贝胺5,15,25mg·kg-1(ig)可明显缩短小鼠6min内不动时间
短句来源
     CTN-T(20~60 mg·kg~(-1),po,twice per day for 4 d) had the same effect in rats.
     kg-1缩短游泳不动时间; 在大鼠强迫游泳实验中,CTN-T连续4 d灌胃(每天2次)20~60mg.
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  相似匹配句对
     Time is...
     时间
短句来源
     Time
     时间
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     the motionless time of servomotor Tq=0.14 s;
     接力器不动时间Tq=0.14s;
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     Fixed Point on Partially Ordered Sets
     偏序集上的不动
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  immobility time
When the animals were 1-3 months of age, the open field behavior was changed, immobility time in the Porsolt's swim test was lengthened, and voluntary alcohol consumption was increased in the propranolol-treated rats.
      
On the other hand, all of the drugs tested reduced immobility time in rats exposed to a pretest session.
      
Furthermore, desipramine reduced immobility time in rats pre-exposed to types of stress different from forced swimming, cold, restraint or foot-shock.
      
The 5-HT1A agonists 8-OH-DPAT (0.125-1.0 mg/kg, SC) and tandospirone (SM-3997) (5-20 mg/kg, SC) both produced dose-related decreases in immobility time following subchronic treatment in rats.
      
The benzodiazepine diazepam (5 mg/kg) also failed to reduce immobility time, suggesting that anxiolytic properties of 5-HT1A agonists did not mediate this behavioral effect.
      
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The antidepressant effects of the N-Isosuccinyl-dichlorocinnamo-ylamide ( 7903 ) , an analogue of piperine, upon 5 animal models were studied. The 7903 was found to have antidepressant effects on the models with doses less than TD50. The 7903 with the single dose, which did not increase the spontaneous motor activity of animals, could significantly decrease the duration of immobility of mice and rats in the forced-swimming test and that of mice in the tail-suspension test. The duration of the longest permanent...

The antidepressant effects of the N-Isosuccinyl-dichlorocinnamo-ylamide ( 7903 ) , an analogue of piperine, upon 5 animal models were studied. The 7903 was found to have antidepressant effects on the models with doses less than TD50. The 7903 with the single dose, which did not increase the spontaneous motor activity of animals, could significantly decrease the duration of immobility of mice and rats in the forced-swimming test and that of mice in the tail-suspension test. The duration of the longest permanent immobility indaced by cornea electro-stimulation in mice was also decreased with the chronic administration ( 2 weeks ) of the 7903. And the hypothermia induced by reserpine could be antagonized by the 7903.

研究一种新的胡椒碱衍化物:3,4—二氯苯丙烯酰另丁胺(7903)对五种抑郁动物模型的影响。7903在小于TD_(50)剂量下,对所用动物模型均显示出抗抑郁效应,即在不增加动物的自主活动情况下,急性ip 7903可明显缩短小鼠及大鼠强迫游泳不动状态时间;急性ip或po明显缩短小鼠悬尾不动时间;慢性(二周)ip可明显缩短电刺激小鼠角膜引起的最长持续不动状态时间;急性ip可明显改善利血平引起的小鼠体温下降。

The effects of domestic moclobemide on animal model of depressant and monoamine oxidase type A(MAO-A) activity were studied. 5~20mg· kg-1 ig moclobemide prevented dose-dependently blepharoptosis induced by reserpine(2.8mg·kg-1, sc) in rat. 5 ̄25mg·kg-1(ig)moclobemide significantly decreased the duration of immobility in" dispair" test in mouse. Domestic moclobemide in dose 6~24 mg·kg-1(ig) demonstrated dose-dependent inhibitory effect on MAO-A activity in mouse brain tissues. When the mice were orally given moclobemide...

The effects of domestic moclobemide on animal model of depressant and monoamine oxidase type A(MAO-A) activity were studied. 5~20mg· kg-1 ig moclobemide prevented dose-dependently blepharoptosis induced by reserpine(2.8mg·kg-1, sc) in rat. 5 ̄25mg·kg-1(ig)moclobemide significantly decreased the duration of immobility in" dispair" test in mouse. Domestic moclobemide in dose 6~24 mg·kg-1(ig) demonstrated dose-dependent inhibitory effect on MAO-A activity in mouse brain tissues. When the mice were orally given moclobemide 24 mg· kg-1(ig),the moclobemide induced maximum MAOA inhibition by 74.4% 2 h after drug treatment, and the enzyme activity had almost recovered completely by 16 h.

研究国产吗氯贝胺对抑郁动物模型和单胺氧化酶-A(MAO-A)活性的影响。吗氯贝胺5、10、20mg·kg-1(ig)可显著对抗利血平(2.8mg·kg-1,sc)引起的大鼠眼睑下垂,其抑制率分别为60%,80%与90%。在小鼠获得性“绝望”实验中,吗氯贝胺5,15,25mg·kg-1(ig)可明显缩短小鼠6min内不动时间。本研究尚证实,吗氯贝胺6,12,24mg·kg-1(ig)可抑制小鼠脑组织中MAO-A活性,并与剂量呈明显依赖关系。一次给予小鼠24mg·kg-1(ig),2h后吗氯贝胺对MAO-A活性的抑制作用达高峰(74.7%),4h后MAO-A活性开始有所恢复,于用药后16h活性已基本趋于正常。

Effects of moelobemide (Moc)on thebehdvior of mice and rats in the forced swimming test,an animal model predictive for antidepressant activity,were examincd.In micc.acute administration of Moc(30,100 and 300 mg·kg ̄(-1) ig once,or 10,30 and 100mg·kg ̄(-1)ig, 3 times in 24 h) did not show anv effectson theduration of immobility,while daily treatment(10,30 and 100 mg·kg ̄(-1)ig, once a day for 20 d)dose-dependently reduced the immobility time to88%, 71 % and 59%of the controls respectively with-out stlmulation of...

Effects of moelobemide (Moc)on thebehdvior of mice and rats in the forced swimming test,an animal model predictive for antidepressant activity,were examincd.In micc.acute administration of Moc(30,100 and 300 mg·kg ̄(-1) ig once,or 10,30 and 100mg·kg ̄(-1)ig, 3 times in 24 h) did not show anv effectson theduration of immobility,while daily treatment(10,30 and 100 mg·kg ̄(-1)ig, once a day for 20 d)dose-dependently reduced the immobility time to88%, 71 % and 59%of the controls respectively with-out stlmulation of motor activity. In rats, a single injec-tion of Moc(10,30 and 100 mg·kg ̄(-1) ip) showed noeffects.It was observed that the immobility time wassignificantly decreased to 37% and 64%of the con-trols with 30 and 100 mg·kg ̄(-1)of Moc administrated3 times in 24 h respectively. In the chronic experiments(ig,twice a day for 15 d), Moc(10, 30 and 100 mg·kg  ̄(-1))dose-dependently reduced the duration ofimmobility to 75 %。 65 % and 44% of the controlsrespectively with milder decrease of locomotion in,theopen field.Imipramine(10 mg·kg ̄(-1)), as a comparda-tive drug, showed the same resuIts except the resultthat the anti-immobility effect in mice was not poten-tiated by chronic treatment as compared to acute ad-ministration perhaps owing to the strain difference Inconclusion,th ereversible monoamine oxidase Ainhibitor Moc.active in the forced swimming test,but the effects are significant and dose-dependent inthe chronic treatments.

用大鼠和小鼠强迫游泳行为模型观察了吗氯贝胺的抗抑郁效应。大鼠一次给予吗氯贝胺10-100mg·kg ̄(-1)无影响。24h内3次强化给药使游泳不动时间减少。若每日给药2次。连续15次则不但效应进一步加强且呈较好的量效关系,同时活动性不增加。小鼠单次或3次强化给予吗氯贝胺对游泳不动时间均无明显影响。每日1次。连续给药20d,表现出与大鼠同样的良好效应和量效关系。活动性亦无增高。

 
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