Somberg J, Cagin N, Levitt B, Bounous H, Ready P, Leonard D, Anagnostopoulos C
J Pharmacol Exp Ther. 1978 Jan;204(1):226-9.
Myocardial uptake of doxorubicin (Adriamycin) and its inhibition by digoxin and propranolol were studied in paced, isolated perfused cat hearts using tritiated doxorubicin. Contractility was studied using a Walton-Brody strain gauge arch and its first derivative. Coronary blood flow was measured by collecting the effluent from the heart. The myocardial content of doxorubicin was 0.069 +/- 0.101 nmol/mg after 30 minutes. Combined administration of doxorubicin and digoxin reduced the myocardial content of doxorubicin to 0.025 +/- 0.010 nmol/mg (P less than .02). The combination increased contractility compared with doxorubicin alone and increased coronary blood flow compared with digoxin alone. The reduction in the myocardial content of digoxin by doxorubicin was not significant. Propranolol also reduced the myocardial uptake of doxorubicin (P less than .05) without changing coronary blood flow and without further reducing contractility. Thus, both propranolol and digoxin merit evaluation in preventing doxorubicin cardiotoxicity.
使用氚标记的阿霉素,在有起搏的离体灌注猫心脏中研究了阿霉素(阿霉素)的心肌摄取及其被地高辛和普萘洛尔的抑制作用。使用沃尔顿 - 布罗迪应变仪弓及其一阶导数研究收缩性。通过收集心脏流出液来测量冠状动脉血流量。30分钟后阿霉素的心肌含量为0.069±0.101 nmol/mg。阿霉素和地高辛联合给药使阿霉素的心肌含量降至0.025±0.010 nmol/mg(P<0.02)。与单独使用阿霉素相比,联合用药增加了收缩性,与单独使用地高辛相比,增加了冠状动脉血流量。阿霉素对地高辛心肌含量的降低不显著。普萘洛尔也降低了阿霉素的心肌摄取(P<0.05),而不改变冠状动脉血流量,也不进一步降低收缩性。因此,普萘洛尔和地高辛在预防阿霉素心脏毒性方面都值得评估。