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   镇痛 的翻译结果: 查询用时:0.074秒
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镇痛     
相关语句
  analgesia
     The Effect of Analgesia and Immunologic Modulation by HSV-I Amplicon Vector Transferring HPPE to Rats CNS
     HSV-I扩增子载体转移HPPE基因在大鼠中枢神经系统镇痛效应及对免疫功能影响的研究
短句来源
     Experimental Study of the Relationships between Nitric Oxide and Morphine Analgesia and Tolerance
     一氧化氮与吗啡镇痛作用及其镇痛耐受关系的实验研究
短句来源
     Role of SP、CGRP、NO in Tooth Nociception and TENS Analgesia
     SP、CGRP、NO在牙齿伤害性感受过程及TENS镇痛中的作用
短句来源
     Study on the Local Analgesia Mechanism of μ-opioid Receptors and Clinical Utility in Periphery
     μ-阿片受体外周部位镇痛机理的基础和临床应用研究
短句来源
     STUDIES ON THE RELATIONSHIP BETWEEN ADRENAL CORTICOS-TEROIDS AND ACUPUNCTURE ANALGESIA.Ⅱ.CLINICAL STUDY OF GLUCOCORTICOSTEROIDS
     肾上腺皮质激素与针刺镇痛关系的研究——Ⅱ.糖皮质激素在临床针麻中的作用
短句来源
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  analgesic
     Purification of Analgesic C4 Component of Toxin of Agkistrodon Halys Pallas and Its Modulation on Endogenous Opiate Peptides
     江浙蝮蛇毒镇痛C4组分提取纯化及其对内阿片肽调控机理研究
短句来源
     Study on Analgesic and Gastroprotective Effects of Amtolmetin Guacyl and Its Mechanisms of Action
     呱氨托美汀镇痛和胃保护作用及其部分机制的研究
短句来源
     Study on the Analgesic and Anti-inflammation of Compound Ketoprofen
     复方酮洛芬镇痛抗炎药的研究
短句来源
     STUDIES ON POTENT ANALGESICS Ⅱ.Synthesis and Analgesic Activity of the Derivatives of 3-Methyl Fentanyl
     强效镇痛剂研究——Ⅱ.3-甲基芬太尼类衍生物的合成及镇痛活性
短句来源
     THE RELATIONSHIP BETWEEN ANALGESIC ACTIVITY AND STRUCTURE OF SOME ASPARAGINYL PEPTIDES
     含门冬酰胺肽类的镇痛活性与结构的关系
短句来源
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  analgesic effect
     The average time for onset of the analgesic effect for the three drugs were 18. 7± 10. 5, 19. 1± 8. 1and 12. 2±4. 6 minutes respectively and the average duration of the analgesic effect was 7. 2±2. 1,3. 6±1. 6 and 5. 8±2. 7 hours.
     镇痛起效时间分别为18.7±10.5分钟,19.1±8.1分钟和12.2±4.6分钟; 镇痛时间分别为7.2±2.1小时.3.6±1.6小时和5.8±2.7小时。
短句来源
     The average inhibitory duration of 9 pain-inhibited neurons decreased from (5.34±0.56) s to (2.41±0.89) s, the tail-flick latency was prolonged from (4.11±0.38) s to (8.01±0.59) s, i.e. displayed a analgesic effect of electroacupuncture.
     9个痛抑制神经元平均抑制时程从电针前(5.34±0.56)s减少至(2.41±0.89)s,甩尾潜伏期从(4.11±0.38)s延长到(8.01±0.59)s,即呈现出电针的镇痛效应。
短句来源
     Analgesic effect of ~(89)SrCl_2 on metastatic cancer of bone
     ~(89)SrCl_2治疗骨89转移癌镇痛效果分析
短句来源
     In mouse 55℃ hot plate test, SO3(0.65-5μgkg~(-1), icv)as well as MⅦA(0.39-5μgkg~(-1), icv)exhibited powerful analgesic effect(100%).
     SO3(0.65-5μg·kg~(-1),icv)和MⅦA(0.39-5μg·kg~(-1),icv)在小鼠55℃热板测痛模型上均表现出显著性的镇痛效果,最大镇痛效应均可达100%;
短句来源
     The duration of analgesic effect in theexperimental group was significanly longer (376±842 sec) than that in the control group(2415 ± 380 sec) (P<0. 05).
     镇痛持续时间,在实验组为3761±842秒,对照组为2415±380秒(P<0.05)。
短句来源
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  pain
     Epidural Injection of Morphine as an Adjunct to Plegicil in Alleviating Cancer Pain
     硬膜外腔注射吗啡辅助乙酰普马嗪用于晚期癌症镇痛
短句来源
     Analgesic activity of buprenorphine in gynecological postoperative pain
     丁丙诺啡用于妇科术后镇痛
短句来源
     The Effect of Dolantin and Acupuncture on the Pain Components P200-N300 of Somatosensory Evoked Potentials of Median Nerve
     针刺及药物镇痛对正中神经体感诱发电位痛成份P200-N300的影响
短句来源
     Morphological Studies on the Relationship Between Primary Pain Afferent and the Changes of Ache Activity in the Spinal Cord of Rats During Electroacupuncture and Morphine Analgesia
     电针及吗啡镇痛大鼠脊髓内AChE的改变与痛觉一级传入关系的形态学研究
短句来源
     A Clinical Study on Cancer Pain Treated with "Analgesic Powder for Cancer"
     癌症镇痛散治疗癌性疼痛临床研究
短句来源
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  analgesia
In most experimental and clinical studies, opioid-mediated analgesia proved to be accompanied by immunosuppression.
      
There exists significant individual variation in electroacupuncture (EA) induced analgesia.
      
Rats may be classified as high- and lowresponders according to their response to EA analgesia.
      
It is concluded that the spinal release of CCK-8 may be one of the key factors determining the effect of EA analgesia.
      
Interleukin-2 mediates the peripheral analgesia of interferon alpha
      
更多          
  analgesic
Though only two esters showed antiinflammatory activity similar to that of the parent drug at equivalent dose levels, all the esters were equipotent to indomethacin in the mouse acetic acid-induced writhing assay for analgesic action.
      
By modifying the chemical structure of opioid ligands, it is possible to preserve the analgesic effect and avoid the development of immunosuppression.
      
Study of the relationship between analgesic activity and structure of synthetic melanocortin analogs
      
In this work, the relationship between analgesic activity of the peptide and its structure was studied.
      
Truncations of the N-terminal residues eliminated the analgesic activity.
      
更多          
  analgesic effect
By modifying the chemical structure of opioid ligands, it is possible to preserve the analgesic effect and avoid the development of immunosuppression.
      
Coadministration of the dipeptide and naloxone or naloxone methiodide insignificantly decreased the dipeptide analgesic effect in the tail-flick and acetic acid writing tests.
      
Introduction of an isopropyl residue into the C-terminal amide of the Nle2 analogue resulted in the appearance of anxiogenic and antialcohol activity and the ability to increase the morphine analgesic effect in the tail-flick test on rats.
      
Relationship between the analgesic effect of electroacupuncture and CCK-8 content in spinal perfusate in rats
      
Furthermore, the analgesic effect of IFN-α is reversible by monoclonal anti-IL-2 antibody.In vitro experiments show that IFN-α significantly increases the production of IL-2 in a dose dependent manner.
      
更多          
  pain
The pain threshold of the mice was then investigated by hot-plate test (HPPT).
      
NMDA 0.05 μg or AMPA 0.05 μg decreased the pain threshold slightly but did not differ in effect compared with the aCSF group; 2 μg MK-801 or 0.5 μg NBQX both increased the pain threshold significantly.
      
The Opioidergic System in the Combined Regulation of Pain and Immunity
      
Opioid receptors of μ, δ, and κ types are involved in the mechanisms of combined regulation of pain and immunity, with μ and δ receptors suppressing the immune response and κ receptors enhancing it.
      
The opioidergic mechanisms are coupled with nonopioid peptidergic and nonpeptide systems of pain and immunity regulation.
      
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