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CARDIAC HYPERTROPHY/CARDIAC FAILURE MOUSE BY TRANSFERRING GENE OF HEPATITIS C VIRUS

机译:转移丙型肝炎病毒基因的心脏肥大/心脏衰竭小鼠

摘要

PROBLEM TO BE SOLVED: To attain the smooth supply of mice as a Homo sapiens disease model mouse for elucidation of the mechanism of pathogenesis, prophylaxis, diagnosis, treatment, or the like, of cardiac hypertrophy/cardiac failure caused by HCV (hepatitis C virus), further can widely and repeatedly utilize the mouse as an experimental material of cardiac failure and cardiac hypertrophy caused by HCV and can promote the study relating to the elucidation of the mechanisms of pathogenesis, prophylaxis, diagnosis, treatment, or the like, of cardiac hypertrophy/cardiac failure caused by HCV and cell level of studies thereon.;SOLUTION: An HCV gene is transferred into a cardiac hypertrophy/cardiac failure mouse so that (1) at 24 weeks of age, abnormal cardiac function cannot clearly be observed and (2) at 48 weeks of age, decrease of systolic arterial pressure, increase in heart weight and weight ratio of heart/body, increase in ventricular end-systolic volume, increase in left ventricular end-diastolic volume, decrease in left ventricular ejection fraction and drop of dp/dt may be observed, respectively.;COPYRIGHT: (C)2005,JPO&NCIPI
机译:要解决的问题:为使小鼠成为智人模型小鼠而获得平稳的供应,以阐明由HCV(丙型肝炎病毒)引起的心脏肥大/心脏衰竭的发病机理,预防,诊断,治疗等机理),还可以广泛和反复地将小鼠用作HCV引起的心力衰竭和心脏肥大的实验材料,并可以促进与阐明心脏病的发病机理,预防,诊断,治疗等有关的研究。 HCV引起的肥大/心脏衰竭及其细胞水平研究;解决方案:HCV基因被转移到心脏肥大/心脏衰竭小鼠中,因此(1)在24周龄时,不能清楚地观察到异常的心脏功能,并且( 2)在48周龄时,收缩压降低,心脏重量和心/体重比增加,心室末末收缩容积增加,左心室增加舒张末期容积,左心室射血分数降低和dp / dt下降。COPYRIGHT:(C)2005,JPO&NCIPI

著录项

  • 公开/公告号JP2005137336A

    专利类型

  • 公开/公告日2005-06-02

    原文格式PDF

  • 申请/专利权人 MATSUMORI AKIRA;

    申请/专利号JP20030380569

  • 发明设计人 MATSUMORI AKIRA;

    申请日2003-11-10

  • 分类号A01K1/03;A01K67/027;

  • 国家 JP

  • 入库时间 2022-08-21 22:34:32

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