Calcium channel blockers (CCBs) are anti-hypertensive drugs that ar'/> Effects of amlodipine and lacidipine on cardiac remodelling and renin production in salt-loaded stroke-prone hypertensive rats
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Effects of amlodipine and lacidipine on cardiac remodelling and renin production in salt-loaded stroke-prone hypertensive rats

机译:氨氯地平和拉米地平对易发盐盐性卒中高血压大鼠心脏重塑和肾素生成的影响

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摘要

class="enumerated" style="list-style-type:decimal">Calcium channel blockers (CCBs) are anti-hypertensive drugs that are usually considered to act mainly as vasodilators. We investigated the relation between the reduction of blood pressure evoked by two long-acting CCBs and their protective effect against cardiac and renal damage in salt-loaded stroke-prone spontaneously hypertensive rats (SHRSP).SHRSP were exposed to high dietary salt intake (1% NaCl in drinking solution) from 8 to 14 weeks of age, with or without amlodipine or lacidipine at three dosage regimens producing similar effects on blood pressure.The lowest dosages of both drugs had non-significant effects on blood pressure but inhibited the paradoxical increases in plasma renin activity (PRA) and in renin mRNA in kidney that were found in salt-loaded SHRSP. The lowest dosage of lacidipine (but not of amlodipine) restored the physiological downregulation of renin production by high salt and reduced left ventricular hypertrophy and mRNA levels of atrial natriuretic factor and transforming growth factor-β1.The intermediate dosages reduced blood pressure and PRA in a comparable manner, but cardiac hypertrophy was more reduced by lacidipine than by amlodipine.Although the highest doses exhibited a further action on blood pressure, they had no additional effect on cardiac hypertrophy, and they increased PRA and kidney levels of renin mRNA even more than in the absence of drug treatment.We conclude that reduction of blood pressure is not the sole mechanism involved in the prevention of cardiac remodelling by CCBs, and that protection against kidney damage and excessive renin production by low and intermediate dosages of these drugs contributes to their beneficial cardiovascular effects.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 钙通道阻滞剂(CCB)是抗高血压药,通常被认为主要起血管扩张剂的作用。我们研究了两种长效CCB引起的血压降低与其对盐易中风自发性高血压大鼠(SHRSP)的心脏和肾脏损害的保护作用之间的关系。 SHRSP至8周龄的高饮食盐摄入量(饮用水中的NaCl浓度为1%),有或没有氨氯地平或lacidipine的三种剂量方案对血压产生相似的影响。 两者的最低剂量这些药物对血压没有显着影响,但抑制了盐加载的SHRSP中发现的血浆肾素活性(PRA)和肾脏中肾素mRNA的反常增加。最低剂量的拉西地平(但不是氨氯地平)可以通过高盐恢复肾素的生理下调,并减少左心室肥大和心钠素和转化生长因子-β1的mRNA水平。 中等剂量可以降低血压和PRA,但是拉西地平比氨氯地平对心脏肥大的抑制作用更大。 尽管最高剂量对血压有进一步的作用,但对心脏肥大没有附加作用,并且他们使PRA和肾素mRNA的水平甚至比没有药物治疗时更高。 我们得出的结论是,降低血压并不是CCB预防心脏重塑的唯一机制,并且低剂量和中等剂量的这些药物对肾脏损害和肾素过多产生的保护作用有助于其有益的心血管作用。

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