Van Vleet J F, Herman E H, Ferrans V J
Exp Mol Pathol. 1984 Aug;41(1):10-25. doi: 10.1016/0014-4800(84)90003-0.
Minoxidil, a vasodilating antihypertensive drug, was given orally at 10 mg/kg daily for 2 days to twelve 25- to 35-kg miniature pigs. Twelve control pigs were also studied. Minoxidil-treated pigs had tachycardia and hypotension and were killed 24 hr after the second dose. Gross examination showed diffuse hemorrhage in left atrial epicardium in all pigs, and also in ventricular epicardium (2 of 12 pigs) and endocardium (3 of 12 pigs). Pale areas of necrosis were observed on incision of the left ventricular papillary muscles in 3 pigs. Light and electron microscopic studies showed acute vascular damage with hemorrhage in the left atrial epicardium. Affected arterioles had endothelial cell swelling and transmural and perivascular accumulations of leukocytes, edema fluid, fibrin clumps, and erythrocytes. The swollen endothelial cells had large, irregularly shaped nuclei with abundant euchromatin; mitotic figures were frequent. The cytoplasm contained numerous polysomes and cisterns of rough endoplasmic reticulum. Fibroblasts adjacent to damaged vessels had edematous cytoplasm and increased amounts of rough endoplasmic reticulum. In the affected left ventricular papillary muscles, necrotic myocytes showed contraction bands, mitochondrial matrical densities, lipid accumulation, initial lysis of I bands, and pyknotic nuclei. The lesions were judged to result from two mechanisms: (1) hemorrhagic lesions from drug-induced vascular injury centered on epicardial and subepicardial arterioles and (2) papillary muscle necrosis from ischemic injury from hypoperfusion during minoxidil-induced tachycardia and hypotension.
将血管扩张性抗高血压药物米诺地尔以每日10毫克/千克的剂量口服,连续给药2天,用于12头体重25至35千克的小型猪。还对12头对照猪进行了研究。接受米诺地尔治疗的猪出现心动过速和低血压,并在第二次给药后24小时处死。大体检查显示,所有猪的左心房心外膜均有弥漫性出血,12头猪中的2头心室心外膜和3头心内膜也有出血。3头猪在切开左心室乳头肌时观察到苍白的坏死区域。光镜和电镜研究显示左心房心外膜有急性血管损伤伴出血。受影响的小动脉内皮细胞肿胀,白细胞、水肿液、纤维蛋白团块和红细胞在血管壁和血管周围积聚。肿胀的内皮细胞核大、形状不规则,常染色质丰富;有丝分裂象常见。细胞质中含有大量多核糖体和粗面内质网池。受损血管附近的成纤维细胞胞质水肿,粗面内质网增多。在受影响的左心室乳头肌中,坏死的心肌细胞出现收缩带、线粒体基质密度增加、脂质积聚、I带初始溶解和核固缩。这些病变被认为是由两种机制引起的:(1)以心外膜和心外膜下小动脉为中心的药物诱导血管损伤导致的出血性病变;(2)米诺地尔诱导的心动过速和低血压期间低灌注引起的缺血性损伤导致的乳头肌坏死。