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Inflammation Alters Angiotensin Converting Enzymes (ACE and ACE-2) Balance in Rat Heart

机译:炎症改变大鼠心脏中血管紧张素转换酶(ACE和ACE-2)的平衡

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Angiotensin converting enzymes (ACE) and more recently discovered ACE-2 are important proteins involved in the renin–angiotensin system. The balance between ACE and ACE-2 is important for the regulation of blood pressure and electrolyte homeostasis. Inflammatory diseases like rheumatoid arthritis are associated with increased risk for cardiovascular complications. We studied the effect of inflammation on the expression levels of ACE and ACE-2 in two groups (n = 4/group) of adjuvant arthritis (AA) and healthy (control) rats. The AA group received 0.2 ml of 50 mg ml−1 of Mycobacterium butyricum suspended in squalene into the tail base. On day 12, rats were euthanized and their organs (hearts, liver, kidney, and intestine) were excised. The mRNA of ACE and ACE-2 were determined by real-time polymerase chain reaction. ACE and ACE-2 protein expression in rat heart was determined by Western blot. Inflammation resulted in 80% reduction of ACE-2 gene expression in rat heart. ACE-2/ACE expression ratio was significantly reduced from 0.7 ± 0.4 in control rats to 0.07 ± 0.09 in AA. Similarly, ACE-2/ACE protein expression ratio was also disrupted with a significant reduction in AA animals (6.7 ± 4.8 vs. 0.9 ± 05 in control and AA, respectively). ACE-2 has been found to provide negative feedback of renin–angiotensin system and protection of the heart and kidneys. Disruption of the balance between ACE and ACE-2 observed in inflammation may be, at least in part, involved in the cardiovascular complications seen in patients with inflammatory diseases.
机译:血管紧张素转换酶(ACE)和最近发现的ACE-2是参与肾素-血管紧张素系统的重要蛋白质。 ACE和ACE-2之间的平衡对于调节血压和电解质稳态起重要作用。类风湿关节炎等炎症性疾病与心血管并发症的风险增加有关。我们研究了炎症对两组(n = 4 /组)佐剂性关节炎(AA)和健康(对照)大鼠中ACE和ACE-2表达水平的影响。 AA组接受0.2ml的50mg ml sups-1悬浮在角鲨烯中的丁酸分枝杆菌到尾巴中。在第12天,对大鼠实施安乐死并切除其器官(心脏,肝,肾和肠)。通过实时聚合酶链反应测定ACE和ACE-2的mRNA。通过蛋白质印迹法测定大鼠心脏中的ACE和ACE-2蛋白表达。炎症导致大鼠心脏中ACE-2基因表达降低80%。 ACE-2 / ACE表达比从对照组的0.7±0.4显着降低至AA的0.07±0.09。同样,ACE-2 / ACE蛋白的表达比例也被破坏,AA动物显着减少(对照组和AA分别为6.7±4.8和0.9±05)。已经发现ACE-2可以提供肾素-血管紧张素系统的负反馈,并保护心脏和肾脏。在炎症中观察到的ACE和ACE-2之间平衡的破坏可能至少部分与炎症性疾病患者的心血管并发症有关。

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