...
首页> 外文期刊>European Journal of Pharmacology: An International Journal >Possible mechanism for the anemia induced by candesartan cilexetil (TCV-116), an angiotensin II receptor antagonist, in rats.
【24h】

Possible mechanism for the anemia induced by candesartan cilexetil (TCV-116), an angiotensin II receptor antagonist, in rats.

机译:大鼠血管紧张素Ⅱ受体拮抗剂坎地沙坦西酯(TCV-116)引起的贫血的可能机制。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Candesartan cilexetil (TCV-116), an angiotensin II receptor antagonist, was administered orally to male F344/Jcl and Crj:CD (SD) rats at 1000 mg kg(-1) day(-1) for 1-28 days, and the possible mechanism for the anemia induced by TCV-116 was investigated. In the TCV-116 group, the erythrocyte count, hematocrit value and hemoglobin concentration were decreased by 7-8% as compared with the values in the control group after dosing for 28 days. The plasma and renal erythropoietin levels, the reticulocyte count in the peripheral blood and the erythroid cell count upon bone marrow examination were decreased on day 7, but there were no accompanying histopathological renal lesions. Renal blood flow was increased, and mean blood pressure was decreased after TCV-116. These results suggest that the primary cause of the anemia induced by TCV-116 treatment is the increase in renal blood flow followed by a decrease in erythropoietin production.
机译:将Candesartan cilexetil(TCV-116),一种血管紧张素II受体拮抗剂,以1000 mg kg(-1)day(-1)的剂量口服给予雄性F344 / Jcl和Crj:CD(SD)大鼠1-28天,并研究了TCV-116诱发贫血的可能机制。给药28天后,TCV-116组的红细胞计数,血细胞比容值和血红蛋白浓度与对照组相比降低了7-8%。在第7天,血浆和肾脏促红细胞生成素水平,外周血网织红细胞计数以及骨髓检查后的红系细胞计数均降低,但没有伴随的组织病理学肾脏病变。 TCV-116后,肾血流量增加,平均血压降低。这些结果表明,TCV-116治疗引起的贫血的主要原因是肾血流量增加,随后促红细胞生成素产生减少。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号