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钙作为异丙肾上腺素诱导心肌坏死的介质。

Calcium as mediator of isoproterenol-induced myocardial necrosis.

作者信息

Bloom S, Davis D L

出版信息

Am J Pathol. 1972 Dec;69(3):459-70.

Abstract

Isoproterenol (ISO), a drug which causes an increased strength of myocardial contraction when administered to animals in mug/kg doses, causes myocardial necrosis when given mg/kg doses. Previous studies suggested that necrosis might be due to flooding of the heart muscle cells by calcium. To determine if this is true, and to distinguish between flooding due to release of Ca from sequestered intramyocardial compartments and increased influx from the blood, we have measured total myocardial calcium (Ca) after ISO administration. The concentration of myocardial calcium, measured by atomic absorption spectroscopy after dry ashing, increased within 10 minutes of the intraperitoneal injection of ISO in rats. After 10 minutes the Ca remained constant at its new level for at least 50 minutes if the dose of ISO was 10(2) mug/kg or less but continued to rise at a slower rate than noted during the first 10 minutes if the ISO dose was 10(3) mug/kg or more. As measured 1 hour after ISO administration, the increase in Ca, was proportional to the dose, up to 10(2) mug/kg. At higher doses there was no further increase until the dose exceeded 2 x 10(3) mug ISO/kg. Since the amount of necrosis is proportional to dose from about 10(2) to 10(5) mug/kg, while the changes in Ca are not proportional to dose over this entire range, it is concluded that ISO-induced myocardial necrosis is not mediated exclusively by flooding of heart muscle with plasma-derived calcium, although this is undoubtedly an important factor. This conclusion was further supported by experiments showing that propranolol, at doses which completely suppressed the increase in Ca due to ISO, did not completely prevent necrosis.

摘要

异丙肾上腺素(ISO),一种以微克/千克剂量给动物用药时会增强心肌收缩力的药物,当以毫克/千克剂量给药时会导致心肌坏死。先前的研究表明,坏死可能是由于心肌细胞被钙大量充斥所致。为了确定情况是否如此,并区分是由于心肌内储存的钙释放导致的钙充斥,还是血液中钙流入增加导致的钙充斥,我们在给予ISO后测量了心肌总钙含量(Ca)。通过干灰化后原子吸收光谱法测量的心肌钙浓度,在给大鼠腹腔注射ISO后10分钟内升高。如果ISO剂量为10(2)微克/千克或更低,10分钟后Ca在其新水平保持至少50分钟恒定,但如果ISO剂量为10(3)微克/千克或更高,Ca则以比最初10分钟更慢的速度持续升高。在给予ISO 1小时后测量,Ca的增加与剂量成正比,直至10(2)微克/千克。在更高剂量时,直到剂量超过2×10(3)微克ISO/千克才会进一步增加。由于坏死量在约10(2)至10(5)微克/千克范围内与剂量成正比,而Ca的变化在整个该范围内与剂量不成正比,因此得出结论,ISO诱导的心肌坏死并非仅由血浆来源的钙充斥心肌介导,尽管这无疑是一个重要因素。实验表明,普萘洛尔在完全抑制因ISO导致的Ca增加的剂量下,并未完全预防坏死,这进一步支持了该结论。

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