助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   结肠回肠的 的翻译结果: 查询用时:0.019秒
图标索引 在分类学科中查询
所有学科
更多类别查询

图标索引 历史查询
 

结肠回肠的
相关语句
  相似匹配句对
     Vascular ectasias of the colon
     结肠血管扩张症
短句来源
     Management of Patients with Colon Injury
     结肠损伤的处理
短句来源
     THE AGE ANATOMICAL STUDY OF CHILDREN JEJUNUM AND ILEUM
     小儿空回肠的年龄解剖学研究
短句来源
     RELAXATION EFFECTS OF BERBAMINE ON THE ISOLATED RABBIT ILEUM
     小檗胺松弛家兔离体回肠的作用
短句来源
     Effect of 23-Acetate Alisol B on Ex Vivo Ileum of Guinea Pig
     泽泻醇B对豚鼠离体回肠的影响
短句来源
查询“结肠回肠的”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  coloileal
The potential price to be paid for this advance relates largely to uncertainties concerning the absence of the usual barriers to coloileal reflux and the presence of a stagnant, fecal pouch at the end of the small intestine.
      
This was preceded by a short prodromal period of four weeks, characterized by intermittent diarrhea on the basis of a coloileal tumor fistula.
      
The ascending colon was filled with saline by retrograde flow, and pressures at which coloileal reflux occurred were recorded.
      
To prevent coloileal reflux after ileocecal resection, an ileocolic nipple valve anastomosis was constructed in six patients with Crohn's disease.
      
The observations implied that protection of the terminal ileum from coloileal reflux after ileocecal resection for Crohn's disease may favorably influence the prognosis.
      
更多          


The absorption of quercetin and rutin at different segments of intestine was examined. Seventy two Wistar rats were divided randomly into 3 groups (control group, quercetin group and rutin group), each group was divided into 4 subgroups (duodenum group, jejunum group, ileum group and colon group). Different solutions (1% dimethyl sulfoxide, 20 μmol/L of quercetin and rutin) were perfused respectively. At the end of perfusion, effluent solution samples were analyzed with HPLC. The results showed that both quercetin...

The absorption of quercetin and rutin at different segments of intestine was examined. Seventy two Wistar rats were divided randomly into 3 groups (control group, quercetin group and rutin group), each group was divided into 4 subgroups (duodenum group, jejunum group, ileum group and colon group). Different solutions (1% dimethyl sulfoxide, 20 μmol/L of quercetin and rutin) were perfused respectively. At the end of perfusion, effluent solution samples were analyzed with HPLC. The results showed that both quercetin and rutin could be absorbed at different segments of intestine, but the absorption of rutin was significantly lower than quercetin. On the length basis, the absorption rate of quercetin was colon>ileum>duodenum>jejunum. On the area basis, the absorption rate was ileum>jejunum>duodenum> colon. After the perfusion of quercetin, there were unidentified peaks appearing on HPLC chromatogram. The results suggested that quercetin was derived from intestine and then re\|excreted into intestinal lumen.

为了比较不同肠段对槲皮素及芦丁的吸收情况 ,选用Wistar大鼠 72只 ,随机分为对照组、槲皮素组及芦丁组 ,每组分别进行十二指肠、空肠、回肠及结肠灌流。灌流液分别为 1%的二甲基亚砜溶液 (溶剂 )、2 0 μmol L槲皮素、芦丁溶液。灌流结束后 ,采用高效液相色谱仪分析灌流液中槲皮素或芦丁的含量。结果发现 :十二指肠、空肠、回肠、结肠对槲皮素及芦丁均有吸收 ,芦丁的吸收率显著低于槲皮素。槲皮素单位长度吸收率 :结肠 >回肠 >十二指肠 >空肠 ,单位面积吸收率 :回肠 >空肠 >十二指肠 >结肠。槲皮素肠道灌流后 ,高效液相色谱图中出现新的未知峰 ,推测其为肠粘膜代谢后形成的衍生物重新分泌进入肠腔所致。

Aim To study the enhancement effect and mechanism of sodium N -[8-(2-hydroxybenzyl)amino] caprylate (SNAC - a kind of synthetic enhancer) to insulin (INS) solution in gastrointestine. Methods To determine the enhancement effect of SNAC on INS absorption by oral administration to rats and mice; To study the enhancement mechanism of SNAC by three kinds of methods: delivering SNAC and INS solution to different parts of rats' intestines, adding energy inhibitor 2,4-dinitrophenol (DNP) or P-glycoprotein (P-gp)...

Aim To study the enhancement effect and mechanism of sodium N -[8-(2-hydroxybenzyl)amino] caprylate (SNAC - a kind of synthetic enhancer) to insulin (INS) solution in gastrointestine. Methods To determine the enhancement effect of SNAC on INS absorption by oral administration to rats and mice; To study the enhancement mechanism of SNAC by three kinds of methods: delivering SNAC and INS solution to different parts of rats' intestines, adding energy inhibitor 2,4-dinitrophenol (DNP) or P-glycoprotein (P-gp) inhibitor verapamil (Ver) into SNAC and INS solution. Results SNAC was shown to enhance the gastrointestinal absorption of INS, the intensity of absorption enhancement corresponded to the doses of SNAC. The enhancement of SNAC to INS in different parts of the rat intestine was different (jejunum > colon > ileum). The effect of SNAC on INS absorption increased accordingly. Conclusion The enhancement of SNAC to INS absorption presented dose dependence on SNAC; the absorption process needed energy and related to P-gp efflux.

目的 研究一种合成的吸收促进剂N [8 (2 羟苯基 )氨基 ]辛酸钠 (SNAC)对胰岛素 (INS)溶液胃肠道给药的吸收促进作用及作用机制。方法 小鼠和大鼠灌胃给药考察SNAC对INS溶液的吸收促进作用 ;采用大鼠不同肠段给药、能量抑制剂 2 ,4 二硝基苯酚 (DNP)和P 糖蛋白抑制剂维拉帕米 (Ver)研究SNAC的促吸收作用机理。 结果SNAC可促进INS溶液在消化道的吸收 ,作用大小与SNAC的量成正比 ;SNAC的促吸收作用空肠 >结肠 >回肠 ,随DNP浓度增大而减小 ,随Ver浓度增大而增大。结论 SNAC对INS的吸收促进作用呈剂量依赖 ,需要能量 ,受P 糖蛋白排放影响。

Objective To explore the absorption characteristics and mechanism of nimodipine for various intestinal segments.Methods The absorption kinetics and absorption site were investigated using in situ perfusion method in rats.The effects of pH value,absorption site and drug concentration on nimodipine absorption were studied.Results Nimodipine has no specific absorption site in rat′s intestine.The absorption rate constants were 0.068 7, 0.062 0, 0.048 9, 0.059 7 h -1 at duodenum,jejunum,ileum and colon,respectively.Conclusions...

Objective To explore the absorption characteristics and mechanism of nimodipine for various intestinal segments.Methods The absorption kinetics and absorption site were investigated using in situ perfusion method in rats.The effects of pH value,absorption site and drug concentration on nimodipine absorption were studied.Results Nimodipine has no specific absorption site in rat′s intestine.The absorption rate constants were 0.068 7, 0.062 0, 0.048 9, 0.059 7 h -1 at duodenum,jejunum,ileum and colon,respectively.Conclusions Nimodipine shows absorption behaviour from the whole intestine.The absorption of the drug conforms to the passive transport mechanism and first-order kinetics.The results indicate that nimodipine can be formulated and prepared as sustained-release dosage form.

目的研究尼莫地平在大鼠各肠段的吸收动力学特征。方法采用大鼠在体肠段灌流实验 ,主要从吸收部位、药物浓度、pH值等 3方面对尼莫地平的肠段吸收特性进行研究。结果尼莫地平在大鼠肠道内无特定吸收部位 ,各肠段吸收速率常数按十二指肠、空肠、结肠、回肠顺序依次下降 ,吸收速率常数分别为 0 0 6 87、0 0 6 2 0、0 0 5 97、0 0 4 89h-1。在 4 8~ 14 3μmol·L-1浓度内药物吸收量与浓度呈线性关系 ;在 pH 5 0~ 7 4内药物吸收不受 pH值影响。 结论尼莫地平在大鼠全肠段均有吸收 ,吸收符合一级动力学特征 ,吸收机制为被动扩散 ,适于制备日服 1次缓释给药系统

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关结肠回肠的的内容
在知识搜索中查有关结肠回肠的的内容
在数字搜索中查有关结肠回肠的的内容
在概念知识元中查有关结肠回肠的的内容
在学术趋势中查有关结肠回肠的的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社