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长期给予奥曲肽可改善肝硬化大鼠的门静脉高压和门静脉高压性胃病。

Chronic administration of octreotide ameliorates portal hypertension and portal hypertensive gastropathy in rats with cirrhosis.

作者信息

Chan C C, Lee F Y, Wang S S, Chang F Y, Lin H C, Lin H J, Chu C J, Wu S L, Tai C C, Lee S D

机构信息

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

出版信息

Clin Sci (Lond). 1998 Apr;94(4):367-71. doi: 10.1042/cs0940367.

Abstract
  1. Portal hypertension and hyperdynamic circulation have been postulated to play a role in the pathogenesis of portal hypertensive gastropathy. Administration of octreotide to portal hypertensive rats has been shown to reduce portal pressure and ameliorate hyperdynamic circulation. 2. This study investigated the effects of chronic administration of octreotide on systemic and portal haemodynamics and the development of portal hypertensive gastropathy in carbon tetrachloride-induced cirrhotic rats. 3. After 12 weeks of carbon tetrachloride induction, cirrhotic rats were randomly assigned to receive either placebo (5% dextrose in water) or octreotide (65 micrograms/kg in 5% dextrose in water) subcutaneously twice daily for 10 days. Haemodynamic studies with a thermodilution technique and gastric morphometric analyses were performed at 10 days after treatment. 4. In cirrhotic rats, octreotide treatment induced a significant increase in systemic vascular resistance (2.7 +/- 0.2 versus 3.4 +/- 0.2 mmHg/ml.min-1.100 g-1, P < 0.05) and decrease in portal pressure (12.5 +/- 1.2 versus 9.9 +/- 0.5 mmHg, P < 0.05) compared with placebo-treated rats. In addition, octreotide treatment significantly reduced the mean cross-sectional area of gastric mucosal vessels (2290 +/- 145 versus 1810 +/- 101 micron 2, P < 0.05). 5. This study shows that chronic octreotide treatment ameliorates the development of portal hypertensive gastropathy in cirrhotic rats. The effect of octreotide on portal hypertensive gastropathy may, at least partly, be due to the alleviation of portal hypertension and hyperdynamic circulation.
摘要
  1. 门静脉高压和高动力循环被认为在门静脉高压性胃病的发病机制中起作用。已证明给门静脉高压大鼠注射奥曲肽可降低门静脉压力并改善高动力循环。2. 本研究调查了长期给予奥曲肽对四氯化碳诱导的肝硬化大鼠全身和门静脉血流动力学以及门静脉高压性胃病发展的影响。3. 在四氯化碳诱导12周后,将肝硬化大鼠随机分为两组,分别皮下注射安慰剂(5%葡萄糖水溶液)或奥曲肽(65微克/千克,溶于5%葡萄糖水溶液),每日两次,共10天。在治疗10天后进行热稀释技术血流动力学研究和胃形态计量分析。4. 与安慰剂治疗的大鼠相比,奥曲肽治疗使肝硬化大鼠的全身血管阻力显著增加(2.7±0.2对3.4±0.2 mmHg/ml·min⁻¹·100 g⁻¹,P<0.05),门静脉压力降低(12.5±1.2对9.9±0.5 mmHg,P<0.05)。此外,奥曲肽治疗显著减小了胃黏膜血管的平均横截面积(2290±145对1810±101平方微米,P<0.05)。5. 本研究表明,长期奥曲肽治疗可改善肝硬化大鼠门静脉高压性胃病的发展。奥曲肽对门静脉高压性胃病的作用可能至少部分归因于门静脉高压和高动力循环的缓解。

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