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催醒
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  “催醒”译为未确定词的双语例句
     Effects of Rx781094 and M5050 Complex on Regaining Consciousness Activity and on the Content of β-endorphin in Rats
     Rx781094+M5050对大鼠的催醒作用及其对β-EP含量的影响
短句来源
     THE PHARMACOLOGICAL STUDY OF CUIXINGNING(催醒宁)
     催醒宁的药理学研究
短句来源
     All compounds tested are strong cholinesterase inhibitors. The pI_(50) of compound Ⅱa (R=C_4H_9) is 8.26, more potent than CUI XING NING (R=CH_3).
     化合物Ⅰ~Ⅴ的pI_(50)值在6.72以上,其中Ⅱ(R=C_4H_9)的pI_(50)值高达8.26,较催醒宁(R=CH_3)高一个数量级。
短句来源
     blood plasma, hypothalamus and pituitary. Results:The regain consciousness ED50 value of Rx78 1094 and M5050 was 9.935 mg/kg, and the regain consciousness dose of the complex is 15mg/kg.
     结果显示:Rx781094+M5050对xylazine+DHE麻醉大鼠的催醒ED_(50)值为9.935mg/kg,确定的催醒剂量为15mg/kg。
短句来源
     Vit K_3 was used by slow intravenous injection as an analeptic in balanced anesthesia. Respiratory frequency(f), V_T. state of consciousness, reaction to stimulation and muscular strength were observed respectively at 1 min, 3min,5min,10min and 15min after Vit K_3 injection (1~2mg/kg).
     本文用K_3静脉缓慢注射静吸复合全麻后催醒,K_3用量1~2mg/kg,注药后1min、3min、5min、10min、15min分别监测f、V_T、唤醒情况、对针刺反应、肌力恢复情况,与对照组比较有显著差异(P<0.05)。
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  相似匹配句对
     THE METABOLISM OF CUI XING AN
     安的代谢
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     A FLUOROMETRIC METHOD FOR THE DETERMINATION OF CUI XING AN
     安的萤光测定法
短句来源
     催收 不催
     收 不
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     Preparation of Cuiru Oral Liquid
     乳口服液的研制
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     Reality knocked awake the entrepreneurial dream
     现实敲创业梦
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查询“催醒”译词为用户自定义的双语例句

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Prompt regaining of consciousness is desirable in most surgical patients under general anesthesia as soon as the operation is finished, and the clinical criteria of alertness are well known to all anesthetists. However, in experiments on animals signs used in our daily practice such as response to verbal commands are hardly obtained. Therefore laboratory workers have to find out a clear-cut phenomenon indicating full recovery from narcosis before they set up their program to determine the effectiveness of any...

Prompt regaining of consciousness is desirable in most surgical patients under general anesthesia as soon as the operation is finished, and the clinical criteria of alertness are well known to all anesthetists. However, in experiments on animals signs used in our daily practice such as response to verbal commands are hardly obtained. Therefore laboratory workers have to find out a clear-cut phenomenon indicating full recovery from narcosis before they set up their program to determine the effectiveness of any antagonist in reversal of anesthesia. EEG is not an ideal means, because it is too complicated and sometimes gives indefinite interpretation. We find that the "body-righting reflex" test is helpful in the research of the rat model.

大多数的全麻手术病人,应能作到术后立即清醒为好,麻醉人员对这些临床标志都十分清楚。然而,在动物实验时,常不能获得我们临床实践中所用的那些指标如回答语言命令。因此,在催醒的动物实验之前,实验者必须找到一种明确的标志麻醉完全苏醒的征象。由于脑电图分析过于复杂和不易作出确切解释,因此不能作为理想工具。在大鼠模型的这类研究中,我们发现翻正反射较有帮助。

A series of m-(alkylamino) alkoxylphenyl N,N-dimethyl carbamates were synthesized as potential analeptics in traditional medicine anesthesia. All compounds were tested for toxicity and analeptic activity in experimental animals. The results will be reported elsewhere.Preliminary clinical observations showed that compound Ⅱ_4, introduced under the name of "CUI XING AN", is less toxic and more effective than physostigmine as analeptic in traditional medicine anesthesia.Structure-activity relationships are briefly...

A series of m-(alkylamino) alkoxylphenyl N,N-dimethyl carbamates were synthesized as potential analeptics in traditional medicine anesthesia. All compounds were tested for toxicity and analeptic activity in experimental animals. The results will be reported elsewhere.Preliminary clinical observations showed that compound Ⅱ_4, introduced under the name of "CUI XING AN", is less toxic and more effective than physostigmine as analeptic in traditional medicine anesthesia.Structure-activity relationships are briefly discussed.

合成了一系列二甲氨基甲酸间-(烷氨基)烷氧基苯酯,并进行了实验动物的毒性和中麻催醒试验。初步临床观察表明,化合物Ⅱ_4(现命名为催醒安)比毒扁豆碱的催醒效果好,而毒性小。简要地讨论了结构和生物活性之间的关系。

The present study describes the effects of carbamate anti-cholinesterase agents and other drugs on the binding sites and on the turnover of nicotinic acetylcholine receptors (N-AChR). The direct binding studies with 125I-α-Bungarotoxin have shown that the neostigmine, prostigmine, pyridostigmine, and ambenonium specifically blockada the N-AChR binding sites, but physostigmine has no directly effect on the N-AChR binding sites.Small dose of ambenomine increases degradation rate of surface N-AChR and it decreases...

The present study describes the effects of carbamate anti-cholinesterase agents and other drugs on the binding sites and on the turnover of nicotinic acetylcholine receptors (N-AChR). The direct binding studies with 125I-α-Bungarotoxin have shown that the neostigmine, prostigmine, pyridostigmine, and ambenonium specifically blockada the N-AChR binding sites, but physostigmine has no directly effect on the N-AChR binding sites.Small dose of ambenomine increases degradation rate of surface N-AChR and it decreases the rate of new N-AChR incorporation into membrane. The bindings of sodium phenobabital to N-AChR sites are very similar to those of d-tubocurarine. The parathion(E605)has no direct bindes to N-AChR sites. The density of extrajunc-tional N-AChR sites is increased and the RBI is 1.46.

本文报道用~(125)I—α—银环蛇毒素研究某些药物对N—胆碱受体(N—-AChR)部位的作用及对N—AChR代谢的影响。用~(125)I—α-银环蛇毒素直接结合作用的研究表明:100和500μM新斯的明、美斯的明、甲基新斯的明和吡啶斯的明等对N—AChR部应有不同程度的专一性阻断作用。而毒扁豆碱和催醒宁对N—AChR部位无直接作用。小剂量美斯的明可加快膜受体降解速率和减慢新生N—AChR掺入膜表面。苯巴比妥纳对N—AChR部应的结合作用很类似于筒简毒碱,主要是减少运功终板内的受体部位数,其受体结合指数(RBI)为0.67。对硫磷(E 605)不直接结合N—ACR部位。但增加运动终板外N—AChR部位的密度,其RBI为1.46。

 
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