Ramanadham S, Decker P, Tenner T E
Life Sci. 1983 Jul 18;33(3):289-96. doi: 10.1016/0024-3205(83)90389-2.
Streptozotocin (65 mg/kg) was used to induce diabetes in male Sprague-Dawley rats. Isolated cardiac tissue exhibited a systematic depression in atrial pacemaker function and an enhancement in ventricular function accompanied by a supersensitivity to calcium relative to control animals. beta-Adrenoceptor density was found to be significantly lowered in the treated animals. However, no change in responsiveness of the tissues to isoproterenol was observed. The systematic changes in atria and ventricle were found to be completely and partially reversed respectively, by daily administration of 4-5 units of Ultralente (U-100) insulin, whereas the decrease in beta-adrenoceptor number and supersensitivity to calcium were completely reversed. These results suggest that STZ by itself might not have toxic effects in the heart and that its effects may be overcome by chronic insulin-replacement.
链脲佐菌素(65毫克/千克)被用于诱导雄性斯普拉格-道利大鼠患糖尿病。与对照动物相比,分离出的心脏组织表现出心房起搏功能的系统性抑制和心室功能的增强,同时伴有对钙的超敏反应。发现经治疗的动物体内β-肾上腺素能受体密度显著降低。然而,未观察到组织对异丙肾上腺素的反应性有变化。通过每日注射4 - 5单位的超长效胰岛素(U - 100),发现心房和心室的系统性变化分别完全和部分得到逆转,而β-肾上腺素能受体数量的减少和对钙的超敏反应则完全逆转。这些结果表明,链脲佐菌素本身可能对心脏没有毒性作用,并且其作用可能通过长期胰岛素替代得以克服。