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β受体阻滞剂对大鼠自发性高血压及去甲肾上腺素诱导性高血压心血管结构变化的影响。

Effect of beta-receptor-blocking agents on cardiovascular structural changes in spontaneous and noradrenaline-induced hypertension in rats.

作者信息

Yamori Y, Tarazi R C, Ooshima A

出版信息

Clin Sci (Lond). 1980 Dec;59 Suppl 6:457s-460s. doi: 10.1042/cs059457s.

Abstract
  1. Continuous intravenous noradrenaline infusion for 1 week into rats by osmotic minipumps significantly increased blood pressure and left ventricular weight. 2. Concomitant alpha-receptor-blockade infusion significantly lowered blood pressure and the aortic weight without significant reduction in left ventricular weight. 3. Two beta-receptor-blocking agents in noradrenaline-infused rats normalized left ventricular weight and significantly reduced the aortic weight, although blood pressure was still higher than control non-infused rats. 4. In 7-week-old spontaneously hypertensive rats, propranolol (perorally for 2 weeks) did not lower blood pressure but reduced significantly cardiovascular protein synthesis ([14C]lysine and [3H]uridine incorporation into non-collagen protein and RNA respectively) in both left ventricle and aorta. This effect was in contrast to hydralazine, which normalized blood pressure but did not reduce cardiovascular protein synthesis. 5. Results suggest that beta-receptors play a modulating role in the structural cardiovascular response to blood pressure.
摘要
  1. 通过渗透微型泵对大鼠连续静脉输注去甲肾上腺素1周,可显著升高血压并增加左心室重量。2. 同时输注α受体阻滞剂可显著降低血压和主动脉重量,而左心室重量无显著降低。3. 在输注去甲肾上腺素的大鼠中,两种β受体阻滞剂可使左心室重量恢复正常,并显著降低主动脉重量,尽管血压仍高于未输注的对照大鼠。4. 在7周龄的自发性高血压大鼠中,普萘洛尔(口服2周)未降低血压,但显著降低了左心室和主动脉中心血管蛋白的合成(分别为[14C]赖氨酸和[3H]尿苷掺入非胶原蛋白和RNA)。这一效应与肼屈嗪相反,肼屈嗪可使血压正常化,但不降低心血管蛋白合成。5. 结果表明,β受体在心血管对血压的结构反应中起调节作用。

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