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重组人血清白蛋白治疗肝硬化腹水的有效性:来自动物模型的证据。

Effectiveness of recombinant human serum albumin in the treatment of ascites in liver cirrhosis: evidence from animal model.

作者信息

Horie S, Nagai H, Yuuki T, Hanada S, Nakamura N

机构信息

Central Research Laboratory, The Green Cross Corporation, Hirakata, Osaka, Japan.

出版信息

Gen Pharmacol. 1998 Nov;31(5):811-5. doi: 10.1016/s0306-3623(98)00064-0.

DOI:10.1016/s0306-3623(98)00064-0
PMID:9809484
Abstract
  1. To investigate the effectiveness of recombinant human serum albumin (rHSA) in the treatment of ascites in liver cirrhosis, we examined its effect on rats with carbon tetrachloride-induced liver cirrhosis. 2. Twenty-five percent rHSA was administered intravenously at a dose of 0.25 to 1.0 g/kg for 2 days to rats with liver cirrhosis accompanied by ascites retention and hypoalbuminemia. 3. rHSA dose dependently decreased abdominal circumference, a clinical index of ascites, with significant difference at a dose of 1.0 g/kg. 4. Although there was no significant difference, rHSA increased blood colloid osmotic pressure (b-COP) and urine volume (UV) in a nearly dose-dependent manner, with significant negative correlation between changes from baseline value in these parameters and in abdominal circumference. 5. These findings suggest that rHSA has abdominal circumference-decreasing action associated with b-COP improvement and UV increase and that it could be effective as a therapeutic drug for ascites in patients with liver cirrhosis accompanied by hypoalbuminemia.
摘要
  1. 为研究重组人血清白蛋白(rHSA)治疗肝硬化腹水的有效性,我们检测了其对四氯化碳诱导的肝硬化大鼠的影响。2. 对伴有腹水潴留和低白蛋白血症的肝硬化大鼠静脉注射25%的rHSA,剂量为0.25至1.0 g/kg,持续2天。3. rHSA剂量依赖性地减小腹围,腹围是腹水的临床指标,在剂量为1.0 g/kg时具有显著差异。4. 尽管无显著差异,但rHSA几乎呈剂量依赖性地增加血胶体渗透压(b-COP)和尿量(UV),这些参数相对于基线值的变化与腹围变化之间存在显著负相关。5. 这些发现表明,rHSA具有减小腹围的作用,与b-COP改善和UV增加相关,并且它可能作为治疗伴有低白蛋白血症的肝硬化患者腹水的有效治疗药物。

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Effectiveness of recombinant human serum albumin in the treatment of ascites in liver cirrhosis: evidence from animal model.重组人血清白蛋白治疗肝硬化腹水的有效性:来自动物模型的证据。
Gen Pharmacol. 1998 Nov;31(5):811-5. doi: 10.1016/s0306-3623(98)00064-0.
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