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长期使用奥曲肽和硝酸异山梨酯对门静脉狭窄大鼠血流动力学的影响。

Effect of long-term octreotide and isosorbide dinitrate on haemodynamics in rats with portal vein stenosis.

作者信息

Lin H C, Huang Y T, Cheng Y R, Hou M C, Lee F Y, Chang F Y, Tsai Y T, Lee S D

机构信息

Department of Medicine, Veterans General Hospital-Taipei, Taiwan.

出版信息

Clin Sci (Lond). 1998 Jun;94(6):645-50. doi: 10.1042/cs0940645.

Abstract
  1. Both octreotide and isosorbide dinitrate have been shown to have portal hypotensive effects in animals with portal hypertension. Moreover, in both animals and humans with portal hypertension, the reduction of portal pressure was enhanced when nitrovasodilators were combined with propranolol or vasopressin. The present study was undertaken to evaluate the effect of long-term administration of octreotide and isosorbide dinitrate on haemodynamics in rats with portal vein stenosis. 2. Portal hypertension was induced by portal vein stenosis. Portal hypertensive rats were allocated into one of four groups (eight rats in each group): vehicle group, octreotide group (100 micrograms/kg via subcutaneous injection every 12 h), isosorbide dinitrate group (5 mg/kg via gastric gavage every 12 h) and combined treatment group. Drug was given for eight consecutive days, starting 1 day before surgery. Haemodynamic values were measured using a radioactive microsphere technique. 3. Long-term octreotide treatment decreased portal pressure and improved the hyperdynamic circulation. In contrast, long-term administration of isosorbide dinitrate reduced portal pressure but did not ameliorate vasodilatation. A combination of octreotide and isosorbide dinitrate improved the hyperdynamic circulation with a reduction of portal pressure. In addition, the mean value of portal pressure after combination treatment was significantly lower than in rats receiving octreotide alone. 4. These results showed that, in rats with portal hypertension, long-term combined administration of octreotide and isosorbide dinitrate improved the hyperdynamic circulation together with a more profound reduction of portal pressure than rats receiving octreotide alone.
摘要
  1. 奥曲肽和硝酸异山梨酯在门静脉高压动物模型中均已显示出具有降低门静脉压力的作用。此外,在动物和人类门静脉高压模型中,当硝基血管扩张剂与普萘洛尔或血管加压素联合使用时,门静脉压力的降低更为明显。本研究旨在评估长期给予奥曲肽和硝酸异山梨酯对门静脉狭窄大鼠血流动力学的影响。2. 通过门静脉狭窄诱导门静脉高压。门静脉高压大鼠被分为四组之一(每组八只大鼠):溶剂对照组、奥曲肽组(每12小时皮下注射100微克/千克)、硝酸异山梨酯组(每12小时经胃管给予5毫克/千克)和联合治疗组。从手术前1天开始连续8天给药。使用放射性微球技术测量血流动力学值。3. 长期使用奥曲肽治疗可降低门静脉压力并改善高动力循环。相比之下,长期给予硝酸异山梨酯可降低门静脉压力,但不能改善血管扩张。奥曲肽和硝酸异山梨酯联合使用可改善高动力循环并降低门静脉压力。此外,联合治疗后门静脉压力的平均值显著低于单独接受奥曲肽治疗的大鼠。4. 这些结果表明,在门静脉高压大鼠中,与单独接受奥曲肽治疗的大鼠相比,长期联合给予奥曲肽和硝酸异山梨酯可改善高动力循环,并更显著地降低门静脉压力。

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