Yamashita Junji, Nakajima Kenji, Ohno Yoichi, Kaneshiro Yoshiaki, Matsuo Takato, Tanaka Hitoshi, Kaneko Kenji
Pharmaceutical Research Laboratory, Research Division, Nihon Pharmaceutical Co Ltd, Narita-City, Chiba, Japan.
Eur J Pharmacol. 2008 Jul 28;589(1-3):239-44. doi: 10.1016/j.ejphar.2008.04.065. Epub 2008 May 14.
We investigated the effects of antithrombin, a plasma inhibitor of coagulation factors, in rats with puromycin aminonucleoside-induced nephrosis, which is an experimental model of human nephrotic syndrome. Antithrombin (50 or 500 IU/kg/i.v.) was administered to rats once a day for 10 days immediately after the injection of puromycin aminonucleoside (50 mg/kg/i.v.). Treatment with antithrombin attenuated the puromycin aminonucleoside-induced hematological abnormalities. Puromycin aminonucleoside-induced renal dysfunction and hyperlipidemia were also suppressed. Histopathological examination revealed severe renal damage such as proteinaceous casts in tubuli and tubular expansion in the kidney of control rats, while an improvement of the damage was seen in antithrombin-treated rats. In addition, antithrombin treatment markedly suppressed puromycin aminonucleoside-induced apoptosis of renal tubular epithelial cells. Furthermore, puromycin aminonucleoside-induced increases in renal cytokine content were also decreased. These findings suggest that thrombin plays an important role in the pathogenesis of puromycin aminonucleoside-induced nephrotic syndrome. Treatment with antithrombin may be clinically effective in patients with nephrotic syndrome.
我们研究了抗凝血酶(一种凝血因子的血浆抑制剂)对嘌呤霉素氨基核苷诱导的肾病大鼠的影响,该模型是人类肾病综合征的实验模型。在注射嘌呤霉素氨基核苷(50mg/kg/静脉注射)后,立即每天一次给大鼠静脉注射抗凝血酶(50或500IU/kg),持续10天。抗凝血酶治疗减轻了嘌呤霉素氨基核苷诱导的血液学异常。嘌呤霉素氨基核苷诱导的肾功能障碍和高脂血症也得到了抑制。组织病理学检查显示,对照大鼠肾脏存在严重的肾损伤,如肾小管内有蛋白管型和肾小管扩张,而抗凝血酶治疗的大鼠肾损伤有所改善。此外,抗凝血酶治疗显著抑制了嘌呤霉素氨基核苷诱导的肾小管上皮细胞凋亡。此外,嘌呤霉素氨基核苷诱导的肾脏细胞因子含量增加也有所减少。这些发现表明,凝血酶在嘌呤霉素氨基核苷诱导的肾病综合征发病机制中起重要作用。抗凝血酶治疗可能对肾病综合征患者具有临床疗效。