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   大鼠回肠 的翻译结果: 查询用时:0.031秒
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大鼠回肠
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  rat ileum
     The 5-hydroxytryptamine-containing immunoreactive (5-HT-TR) neurons of the rat ileum were investigated by means of immunohistochemistry,utilizing an antibody against serotonin.
     本文用5-羟色胺(5-HT)抗血清的免疫组织化学方法对大鼠回肠(外纵肌全层铺片标本)内含5-HT免疫反应性(5-HT-IR)神经元进行了观察研究。
短句来源
     Objective To explore the expression and change on the neurokinin A(NKA) of rat ileum during the development.
     目的 探讨神经激肽A(NKA)在大鼠回肠发育中的表达及变化。
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     Effect of GnRH analogue on glucagon secretion in rat ileum
     GnRH类似物对大鼠回肠组织胰高血糖素释放的影响
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     The purpose of this study was to observe the effects of substance P (SP) on the contractile response of longitudinal muscle with myenteric plexus (LM-MP) of rat ileum induced by 5-HT in vitro and to analyse its mechanism.
     本文采用离体大鼠回肠纵行肌-肌间神经丛(LM-MP)标本,观察SP对5-HT引起的LMMP标本收缩效应的影响,并对其作用机制进行了分析。
短句来源
     EFFECTS OF SUBSTANCE P ON THE CONTRACTILE RESPONSE OF LONGITUDINAL MUSCLE OF RAT ILEUM TO 5-HT
     P物质对5-HT引起的大鼠回肠纵行肌收缩效应的影响及其机制分析
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  “大鼠回肠”译为未确定词的双语例句
     Pretreatment with B、C or D 28.0、56.0 μmol/L Ver 0.28 μmol/L significantly antagonized CaCl2-induced contraction of rat isolated ileum.
     B、C、D28.0、56.0μmol/L及Ver0.28μmol/L均抑制离体大鼠回肠对CaCl_2的反应,具显著性差异。
短句来源
     RESULTS: CBD-ligated rats had thinner ileac mucous membrane (232±22) μm vs (362±43) μm and shorter villi (158±22) μm vs (254±39) μm.
     结果梗阻性黄疸时,大鼠回肠壁呈现肌层变薄,黏膜厚度减少[(232±22)μmvs(362±43)μm],肠绒毛变短[(158±22)μmvs(254±39)μm],变细或绒毛融合等形态学改变;
短句来源
     (2)When GnRH analogue Alarelin(from 1. 0X10-8mol/L to 1. 0X 10-6mol/L) was added to the culture medium of ileum tissue, the level of glucagon immunoreactive substance in the medium was increased with the increment of GnRH analogue concentration.
     3.给大鼠回肠灌注浓度为1.0x10一4mol/L的GnRH类似物阿拉瑞林时,回肠液及血中胰高血糖素免疫反应阳性物质的含量均显著增加,与对照组相比具有显著性差异。
短句来源
     Conclusion Ulinastatin has protective effect on rats with hemorrhagic shock by suppressing the apoptosis in ileal mucosa.
     结论乌司他丁可抑制失血性休克大鼠回肠黏膜细胞的凋亡,对失血性休克大鼠起保护作用。
短句来源
     Compared with the normal group, the content of OFR in ileomucosa, hepatic and pulmonary tissues in ACST and choledochostomy group both increased markedly (P<0.05,<0.01,<0.001, separately); the activities of PLA2 were greatly raised (P<0.05,<0.01,<0.001, separately).
     结果急性重症胆管炎大鼠回肠黏膜、肝、肺组织中的OFR含量,与正常组比较显著升高(P值分别为:<0.05,<0.01,<0.001),PLA2活性与正常组比较明显增强(P值分别为:<0.05,<0.01,<0.001)。
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  相似匹配句对
     LOCALIZATION AND QUANTITATIVE ANALYSIS ON THE DEVELOPMENT OF NKA IN THE ILEUM OF RATS
     神经激肽A在大鼠回肠发育中的定位定量分析
短句来源
     The rate of iodine absorption in rat jejunum and ileum is much fast.
     大鼠空、回肠对碘的吸收速率很快;
短句来源
     Participants Brown Norway(BN)rats.
     研究对象BN大鼠
短句来源
     the ileum and the caecum have exuviated.
     回肠、盲肠缩短;
短句来源
     THE HISTOGENESIS OF SPLEEN OF RATS
     大鼠脾脏的组织发生
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  rat ileum
Forskolin and phorbol-12,13-dibutyrate increased KRP phosphorylation at Ser13 from 25 to 100% but did not produce contraction in rat ileum.
      
Unlike selenate uptake, selenite uptake was not Na+ dependent, neither in pig small intestine nor in sheep jejunum and rat ileum.
      
The results clearly show that selenate transport across the BBM of pig jejunum and ileum, sheep jejunum, and rat ileum is partially energized by a transmembrane Na+ gradient.
      
Thus, insulin introduced in the lumen of the rat ileum in conjunction with sodium cholate and aprotinin, appears to be rapidly absorbed by the epithelial cells and transferred to the circulation through a transcytotic pathway.
      
The antagonistic activity of tested drugs against acetylcholine-induced contraction of rat ileum and oxotremorine-induced salivation and tremor in the mouse was also studied.
      
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Loperamide is a novel type of antidiarrheal agent. In mice Loperamide was shown to be a potent blocker of 15-methyl-PGF_(2a)-induced diarrhea and charcoal progression in the intestine. The inhibitory potency of Loperamide was greater than that of morphine and atropine. The results of experiments on isolated smooth muscles showed that Loperamide inhibited the contractive response of rat jejunum to 15-methyl-PGF_(2a). However, it increased the contractive response of uterus to 15-methyl-PGF_(2a). Loperamide in...

Loperamide is a novel type of antidiarrheal agent. In mice Loperamide was shown to be a potent blocker of 15-methyl-PGF_(2a)-induced diarrhea and charcoal progression in the intestine. The inhibitory potency of Loperamide was greater than that of morphine and atropine. The results of experiments on isolated smooth muscles showed that Loperamide inhibited the contractive response of rat jejunum to 15-methyl-PGF_(2a). However, it increased the contractive response of uterus to 15-methyl-PGF_(2a). Loperamide in dose of 2.5×10~(-7) g/ml stimulated but in dose of 10~(-6) g/ml inhibited the spontaneous contraction of rat uterus. Loperamide antagonized the action of 15-methyl-PGF_(2a) on increasing jejunum secretion. This antagonizing effect could not be reversed by naloxane. The LD_(50) of Loperamide in mice was determined to be 77.9 mg/kg by intraperitoneal injection.

氯哌胺(Loperamide)是一种新型止泻药,能拮抗15-M-PGF_(2α)引起的小鼠小肠内碳粉推进加速和腹泻,作用比吗啡和阿托品强,对离体大鼠回肠的抑制作用也比吗啡、阿托品强。氯哌胺能降低肠平滑肌张力,抑制离体大鼠回肠对15-M-PGF_(2α)的反应性,但却增强子宫平滑肌对15-M-PGF_(2α)的反应性。氯哌胺对离体大鼠子宫自发收缩活动低浓度兴奋、高浓度抑制。氯哌胺对15-M-PGF_(2α)促进大鼠空肠水和钠离子分泌也有拮抗作用,此作用不能被纳洛酮翻转。氯哌胺在小鼠的急性半数致死量为77.9 mg/kg。

The stimulating effect of Substance P(SP)on the longitudinal muscle

P 物质(Sp)能引起大鼠回肠纵行肌收缩并呈剂量依赖性。阈上剂量的Sp(10~(-7)M)可以增强Ach、5-HT 的收缩效应;减弱或消除NE 的抑制效应,阈下剂量的Sp(5×10~(-7)M)可以加强5-HT 的收缩效应,但对Ach、NE 无明显影响。结果提示:SP 可能作为兴奋性递质与经典递质一道共同调节消化道的运动,同时,Sp 对5-HT 可能还具有某种调制作用。

The evidence from in vivo studies showed that glucose polymer enhanced intestinal calcium absorption. However, the mechanism with which calcium absorption is increased by glucose polymer administration is not clear. Calcium uptake by isolated everted rat ileal gut sac was used as a technique in an effort to explore the effect of this carbohydrate on calcium uptake under in vitro conditions.As a comparison, ileal sacs were treated with buffer and sugar solutions at an equivalent dose. The results showed that...

The evidence from in vivo studies showed that glucose polymer enhanced intestinal calcium absorption. However, the mechanism with which calcium absorption is increased by glucose polymer administration is not clear. Calcium uptake by isolated everted rat ileal gut sac was used as a technique in an effort to explore the effect of this carbohydrate on calcium uptake under in vitro conditions.As a comparison, ileal sacs were treated with buffer and sugar solutions at an equivalent dose. The results showed that all three sugars, as compared to buffer treatment, enhanced calcium uptake by ileal sacs, lactose 30.7%, glucose polymer 33% and glucose 24.7%, indicating a non-specific mechanism is involved in intestinal calcium absorption.

本文报告了运用翻转的大鼠回肠囊这一体外实验方法测定葡萄糖聚合物对小肠钙吸收影响的研究,并通过与葡萄糖以及乳糖对小肠钙吸收影响的比较,探讨了葡萄糖聚合物的作用机制。实验结果表明,葡萄糖聚合物可明显地促进翻转的游离回肠囊对钙的吸收。乳糖与葡葡糖也有类似的促进作用。与缓冲液相比,促进钙吸收分别达33、30.7及24.7%。提示上述糖溶液的促进钙吸收作用为一种非特异性机制所致的效应。

 
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