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异丙肾上腺素诱导的心脏损伤中,心脏血管紧张素原mRNA和血管紧张素转换酶(ACE)活性的诱导。

Induction of cardiac angiotensinogen mRNA and angiotensin converting enzyme (ACE) activity in isoproterenol-induced heart injury.

作者信息

Ogiku N, Ishida R, Saeki K, Sugiura M

机构信息

Lead Generation Research Laboratory, Tanabe Seiyaku Co., Ltd., Osaka, Japan.

出版信息

Hypertens Res. 1996 Sep;19(3):179-87. doi: 10.1291/hypres.19.179.

Abstract

Effects of isoproterenol (ISO) on the expression of cardiac angiotensinogen mRNA, angiotensin converting enzyme (ACE) activity, and mechanical functions in spontaneously hypertensive rats were investigated. In the acute phase, defined as within 24 h after the subcutaneous injection of ISO 85 mg/kg, cardiac angiotensinogen mRNA was slightly induced, but ACE activity was not. In the subacute phase, defined as within 8 d after ISO treatment on 2 successive d, both angiotensinogen mRNA expression and ACE activity in the heart were markedly induced. ACE activity in serum was not affected by ISO in either phase. In the subacute phase, ISO reduced body weight and blood pressure, increased ventricular weight and calcium content, and impaired cardiac mechanical function. Oral treatment with imidapril (10 mg/kg/d), an ACE inhibitor, 1 h before each ISO treatment and on the following 6 d, improved ventricular hypertrophy, the elevation of the left ventricular end diastolic pressure, the reduction in contractility, and the prolongation of the time constant. Imidapril significantly suppressed both serum and cardiac ACE activity but did not affect cardiac angiotensinogen mRNA expression in the subacute phase. These results indicate that enhancement of cardiac angiotensinogen mRNA and ACE activity is involved in ISO-induced cardiac dysfunction. Imidapril improved ISO-induced cardiac dysfunction, possibly by suppression of the local ACE activity as well as circulating ACE activity.

摘要

研究了异丙肾上腺素(ISO)对自发性高血压大鼠心脏血管紧张素原mRNA表达、血管紧张素转换酶(ACE)活性及机械功能的影响。在急性期,即皮下注射85mg/kg ISO后24小时内,心脏血管紧张素原mRNA略有诱导,但ACE活性未受影响。在亚急性期,即连续两天给予ISO治疗后8天内,心脏中血管紧张素原mRNA表达和ACE活性均明显诱导。两个阶段中血清ACE活性均不受ISO影响。在亚急性期,ISO降低体重和血压,增加心室重量和钙含量,并损害心脏机械功能。在每次ISO治疗前1小时及随后6天,口服依那普利(10mg/kg/d),一种ACE抑制剂,可改善心室肥厚、左心室舒张末期压力升高、收缩力降低及时间常数延长。依那普利在亚急性期显著抑制血清和心脏ACE活性,但不影响心脏血管紧张素原mRNA表达。这些结果表明,心脏血管紧张素原mRNA和ACE活性增强与ISO诱导的心脏功能障碍有关。依那普利改善ISO诱导的心脏功能障碍,可能是通过抑制局部ACE活性以及循环ACE活性实现的。

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