Lack of cardiotoxic effect of isoproterenol in streptozotocin diabetic rats. A morphometric study of isoproterenol induced fibrosis.

O Gøtzsche
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引用次数: 6

Abstract

The well known cardiotoxic effect of isoproterenol (ISO) was investigated in normal and streptozotocin diabetic rats. Seven days after the subcutaneous injection of ISO (15 mg/kg) the hearts were perfusion fixed and 12 sections from each heart were stained (Masson's trichrome). ISO induced myocardial fibrosis was quantified at the light microscopic level according to established morphometric principles. Pulse rate and ST elevation were recorded by EEC (3 standard leads) before and after the ISO injection. Non-diabetic control animals showed marked fibrosis after ISO, but surprisingly the diabetic animals showed no fibrosis after ISO treatment. These findings were in accordance with an ISO induced ST elevation seen only among control animals although both groups showed the same degree of tachycardia. Insulin treatment prevented the protection against ISO and when streptozotocin was injected 24 h after the ISO a normal quantitative and qualitative appearance of the scar tissue was seen. It thus seems that streptozotocin diabetic rats are protected against the toxic effect of ISO, leaving the haemodynamic response unaffected. Which factor in the diabetic metabolism is responsible for the present phenomenon is not known, but a defect in the signal transmission from the beta-receptor to the adenylcyclase is suggested as a possible explanation.

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异丙肾上腺素对链脲佐菌素糖尿病大鼠缺乏心脏毒性作用。异丙肾上腺素诱导纤维化的形态学研究。
在正常和链脲佐菌素糖尿病大鼠中研究了异丙肾上腺素(ISO)的心脏毒性作用。皮下注射ISO (15mg /kg) 7 d后,灌注固定各组心脏,每组心脏12块切片进行马松三色染色。根据已建立的形态计量学原理,在光镜下定量测定ISO诱导的心肌纤维化。在ISO注射前后用EEC(3根标准导联)记录脉搏率和ST段抬高。非糖尿病对照动物在ISO治疗后出现了明显的纤维化,但令人惊讶的是,糖尿病动物在ISO治疗后没有出现纤维化。这些发现与仅在对照动物中看到的ISO诱导ST段抬高一致,尽管两组均表现出相同程度的心动过速。胰岛素治疗阻止了对ISO的保护,当ISO后24小时注射链脲佐菌素时,可以看到疤痕组织的定量和定性外观正常。因此,链脲佐菌素似乎保护糖尿病大鼠免受ISO的毒性作用,使血流动力学反应不受影响。目前尚不清楚糖尿病代谢中的哪个因素导致了这种现象,但β受体到腺苷酸环化酶的信号传递缺陷被认为是一种可能的解释。
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