Ledingham J M, Lees D C
Br J Pharmacol. 1981 Nov;74(3):643-9. doi: 10.1111/j.1476-5381.1981.tb10475.x.
1 In a previous study in conscious rats, orally administered propranolol acutely lowered cardiac output by 30.5% and oxygen uptake by 12.2%, while oxygen extraction rose by 31.5%. The present study is concerned with the way in which the rat meets its oxygen requirements against such a fall in perfusion. 2 The effect of known concentrations of propranolol on haemoglobin-oxygen affinity was studied in vitro. The effect of orally administered propranolol (given acutely and chronically) was then determined and this was related to the concentration of the drug in plasma and red cells. Further studies were made on the action of propranolol on the Bohr effect and on arterial oxygen carriage. 3 In vitro, high concentrations of propranolol (1 x 10(-4) M) influenced haemoglobin-oxygen affinity in a biphasic manner and this was associated with changes in haematocrit and red cell and plasma pH. No change occurred in affinity after acute or chronic oral administration of the drug due to insufficient concentration in the blood. No direct action of the Bohr effect was detected. 4 Arterial oxygen content rose acutely due to an increase in haemoglobin concentration. 5 It is concluded that increased oxygen extraction in propranolol-treated rats is not explained by the actions of the drug on haemoglobin-oxygen affinity.
1 在之前一项针对清醒大鼠的研究中,口服普萘洛尔可使心输出量急性降低30.5%,耗氧量降低12.2%,而氧摄取率升高31.5%。本研究关注的是大鼠在灌注量如此下降的情况下满足其氧需求的方式。2 研究了已知浓度的普萘洛尔在体外对血红蛋白-氧亲和力的影响。然后确定了口服普萘洛尔(急性和慢性给药)的效果,并将其与血浆和红细胞中药物的浓度相关联。还进一步研究了普萘洛尔对玻尔效应和动脉氧运输的作用。3 在体外,高浓度的普萘洛尔(1×10⁻⁴ M)以双相方式影响血红蛋白-氧亲和力,这与血细胞比容、红细胞和血浆pH值的变化有关。由于血液中浓度不足,急性或慢性口服该药物后亲和力未发生变化。未检测到玻尔效应的直接作用。4 由于血红蛋白浓度增加,动脉氧含量急性升高。5 得出的结论是,普萘洛尔处理的大鼠中氧摄取增加不能用该药物对血红蛋白-氧亲和力的作用来解释。