Milei J, Nuñez R, Rapaport M
Acta Cardiol. 1976;31(5):354-70.
Eighty Wistar rats were divided into 4 groups. All of them received 10 mg/kg i.p. isoproterenol (ISP). The animals were sacrificed at 5 min. (groups A and B) and 24 hours (groups C and D). Groups A and C served as control of group B and D. Group B also received 9 mg/kg prenylamine (P), 30 min before ISP and group D 9 mg/kg P, 1 hour before and 1 hour after ISP. Transversal slices of each heart underwent the following procedures: hematoxilineosin, Barbeito-Lopez trichromic, "ischemia stain", acid phosphatase stain and standard electron microscopy. Group A and C showed positivity for ischemic techniques; necrotic and ischemic zones represented, in average 25.1 +/- 1.4% of the myocardial volume. Group B and D (ISP + prenylamine) showed no significant lesions. Group D (ISP + prenylamine, sacrificed at 24 hours) presented complete absence of "infarct-like" lesions in 17 out of the 20 studied animals. No evident changes in acid-phosphatase enzymes were detected. Animals treated with ISP alone presented "contraction bands" at electron microscopy as well as myofibrillar fragmentation. Those receiving also P showed only light alterations, in the electron microscopy specimens. A primary action of ISP on the calcium pump might explain the infarct-like lesions found in our study. The inhibition of these above mentioned lesions by prenylamine, a drug which acts by slowing down the ca transport, also supports this interpretation.
80只Wistar大鼠被分为4组。所有大鼠均腹腔注射10mg/kg异丙肾上腺素(ISP)。在5分钟时(A组和B组)以及24小时时(C组和D组)处死动物。A组和C组作为B组和D组的对照。B组在注射ISP前30分钟还接受了9mg/kg普尼拉明(P),D组在注射ISP前1小时和后1小时接受9mg/kg P。对每只心脏的横向切片进行以下操作:苏木精-伊红染色、Barbeito-Lopez三色染色、“缺血染色”、酸性磷酸酶染色和标准电子显微镜检查。A组和C组的缺血技术呈阳性;坏死和缺血区域平均占心肌体积的25.1±1.4%。B组和D组(ISP+普尼拉明)未显示明显病变。D组(ISP+普尼拉明,24小时处死)在20只研究动物中有17只完全没有“梗死样”病变。未检测到酸性磷酸酶酶的明显变化。单独用ISP处理的动物在电子显微镜下呈现“收缩带”以及肌原纤维断裂。同时接受P的动物在电子显微镜标本中仅显示轻微改变。ISP对钙泵的主要作用可能解释了我们研究中发现的梗死样病变。普尼拉明通过减缓钙转运起作用,该药物对上述病变的抑制也支持了这一解释。