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抗前列腺增生
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  anti-prostatic hyperplasia
     The screening and anti-prostatic hyperplasia activity assessment of novel steroid 5α-reductase inhibitors LTZ-8 and others
     甾体5α-还原酶抑制剂LTZ-8和类似物的筛选及其抗前列腺增生作用(英文)
短句来源
     The objective of this paper is to Study on the therapeutical basis of Rhododendrom micranthum on anti-prostatic hyperplasia action by pharmacology and serum pharmacochemistry methods and to isolate the effective chemical components from the plant;
     第一部分照山白抗前列腺增生药理作用研究目的:研究照山白提取液抗前列腺增生作用,确定照山白抗前列腺增生作用的有效部位,并进一步研究其有效部位的抗炎、镇痛、抗前列腺增生作用。
短句来源
     AIM To screen new anti-prostatic hyperplasia drugs LTZ-8 an d others(testosterone derivatives with different groups at C-3, C-4 and C-17) , which are different structures of steroid 5α-reductase inhibitors.
     目的 为筛选新的不同结构的甾体 5α 还原酶抑制剂LTZ 8等抗前列腺增生药物 (在C 3,C 4,C 1 7具有不同基团的睾酮衍生物 )。
短句来源
     Studies on the Therapeutical Basis of Rhododendrom Micranthum on the Anti-prostatic Hyperplasia Action and Pharmacokenetics of Total Flavonoids from Rhododendrom Micranthum
     照山白抗前列腺增生药效物质基础与药物代谢动力学研究
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  “抗前列腺增生”译为未确定词的双语例句
     Synthesis of SL-89.0519-08
     抗前列腺增生药SL-89.0519-08的合成
短句来源
     Pharmacology and Toxicology Study of Epristeride: A Novel Drug against Benign Prostate Hyperplasia
     新型抗前列腺增生药爱普列特(Epristeride)药理和毒理研究
短句来源
     Objective: To investigate the effect of Qianlie Huichun on the expression of vascular endothelial growth factor(VEGF) in prostate tissues and expound its anti-prostatomegaly action in model rats with prostatic hypertrophy induced by injected testosterone.
     目的 :探计前列回春对实验性大鼠前列腺组织血管内皮生长因子 (VEGF)表达的影响 ,阐明其抗前列腺增生作用。
短句来源
     Experimental Study on Action of Qianliening Tablets on Prostate Hyperplasia and Its Anti-inflammatory and Analgetic Actions
     前列宁片抗前列腺增生与抗炎镇痛实验研究
短句来源
     The results indicate that DDPH may inhibit benign prostatic hyperplasia and improve the urinary flow.
     实验结果提示DDPH有抗前列腺增生及改善尿流率的作用 .
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  相似匹配句对
     The study of Catharsius molossus L.on experimental prostatic hyperplasia
     蜣螂实验性前列腺增生作用研究
短句来源
     The resistant effect of Qianlieping capsule on benign prostatic hyperplasia
     前列平胶囊的前列腺增生作用
短句来源
     Progress in antiproliferation of melatonin on Benign prostatic hyperplasia and prostate neoplasm
     褪黑素前列腺增生前列腺肿瘤的研究进展
短句来源
     Objective: To study the effect of Qianlieshuning tablet's (QLSN) restraining prostate hyperplasia.
     目的 :观察前列舒宁前列腺增生作用。
短句来源
     Analgesic and Anti-inflammatory Actions and Effect of Jinliyou on Benign Prostatic Hyperstrophy in Rat
     金利油的镇痛消炎和前列腺增生作用
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In this paper the pharmacologic effects of Qian Lie Kang Bao (QLKB) were studied. The results indicated that QLKB could significantly inhibit hypertrophy of the prostate and inflammation, and improve microcirculation.

实验结果表明,前列康宝具有明显的抗前列腺增生,抗炎及改善微循环作用。

Objective:To observe the therapeutic effect of Qianlietong(QLT) on experimental prostatic hyperplasia.Methods:Experimental prostatic hyperplasia was produced in the rat and mouse,and the isolated bladder trigone muscle of the rabbit was used for contraction inhibition study.Results:QLT 3 and 6g/kg that administered intragastrically for 3 and 4 weeks, significantly inhibited the prostatic hyerplasia induced by testosterone propionate in rats, and by transplantation of urinary genitaloid sinus in mice respectively.Otherwise,0.6%...

Objective:To observe the therapeutic effect of Qianlietong(QLT) on experimental prostatic hyperplasia.Methods:Experimental prostatic hyperplasia was produced in the rat and mouse,and the isolated bladder trigone muscle of the rabbit was used for contraction inhibition study.Results:QLT 3 and 6g/kg that administered intragastrically for 3 and 4 weeks, significantly inhibited the prostatic hyerplasia induced by testosterone propionate in rats, and by transplantation of urinary genitaloid sinus in mice respectively.Otherwise,0.6% and 1% water suspension of QLT also inhibited the contraction induced by norepinephrine in isolated bladder trigone muscle of the rabbit,the inhibition was 21%~46.1%.Conclusion:QLT significantly inhibits epxerimental prostatic hyperplasia,and decreases the contraction of bladder trigone muscle induced by αadrenoceptor agonist.

目的:探讨前列通对实验性前列腺增生的治疗作用。方法:利用大鼠和小鼠的前列腺增生模型及兔离体膀胱三角肌标本,观察分析前列通的抗前列腺增生作用和机理。结果:每日给前列通3g/kg及6g/kg灌胃,连续3~4周可分别显著抑制丙酸睾丸素引起的大鼠前列腺增生和小鼠尿生殖窦植入性前列腺增生;0.6%及1%前列通水混悬液尚可抑制去甲肾上腺素诱发的兔离体膀胱三角肌收缩作用,抑制率分别达21%及46.1%。结论:前列通具有显著抑制前列腺增生的作用和对抗α受体激动剂诱发的膀胱三角肌收缩的作用

Pharmacodynamical study of Phenoprolamine (PHENOP) on bladder contractility and benign prostatic hyperplasia was performed in mice. PHENOP caused parallel rightward shifts of the phenylephrine (Phe) concentrationcontractile response curves and didn't suppress the maximal contractile response to Phe (pA2=724) in isolated rabbit urinary bladder smooth muscle DDPH decreased the parameters of cystometry in urethaneanesthetized rats Thirty min after PHENOP (250,500 mg/kg, ig) administration, bladder capacity, voiding...

Pharmacodynamical study of Phenoprolamine (PHENOP) on bladder contractility and benign prostatic hyperplasia was performed in mice. PHENOP caused parallel rightward shifts of the phenylephrine (Phe) concentrationcontractile response curves and didn't suppress the maximal contractile response to Phe (pA2=724) in isolated rabbit urinary bladder smooth muscle DDPH decreased the parameters of cystometry in urethaneanesthetized rats Thirty min after PHENOP (250,500 mg/kg, ig) administration, bladder capacity, voiding pressure,voiding threshold pressure were significantly decreased In the experiment of testosterone propionatesinduced prostatic hyperplasia of mice, PHENOP (125,250 and 500 mg/kg, ig for 4 weeks) could also inhibit the development of benign prostatic hyperplasia in rat PHENOP may be of clinical values in the treatment of benign prostatic hyperplasia and improve the urinary flow in such cases

进行盐酸菲洛普(Phenoprolamine,PHENOP)对大鼠膀胱内压及前列腺增生的药效学研究。结果发现,在离体兔膀胱颈平滑肌,苯肾上腺素(Phe)能增加平滑肌收缩力,PHENOP能浓度依赖性地使Phe的量效曲线平行右移,且最大反应不变(pA2=7.24);PHENOP25.0、50.0mg/kg灌胃能改变正常麻醉大鼠膀胱内压图,使膀胱容积、排尿压、排尿阈值压显著降低;在用丙酸睾丸素引起大鼠前列腺增生的实验中,PHENOP12.5、25.0及50.0mg/kg灌胃4周还可抑制大鼠前列腺组织的增生。提示,PHENOP作为抗前列腺增生药及改善尿流率的药物可能有应用前景

 
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