Manikandan Panchatcharam, Sumitra Miriyala, Nayeem Mohammed, Manohar Bhakthavatsalam Murali, Lokanadam Beema, Vairamuthu Subbiah, Subramaniam Samu, Puvanakrishnan Rengarajulu
Department of Biotechnology, Central Leather Research Institute, Adyar Chennai-600020, India.
Mol Cell Biochem. 2004 Dec;267(1-2):47-58. doi: 10.1023/b:mcbi.0000049364.56230.ea.
In vivo models of myocardial infarction induced by coronary artery ligation (CAL) in rats usually suffer from high early mortality and a low rate of induction. This study investigated the time course initiation of chronic myocardial infarction (CMI) in albino rats and the possibility of reducing early mortality rate due to myocardial infarction by modification of the surgical technique. CAL was carried out by passing the suture through the epicardial layer around the midway of the left anterior descending coronary artery including a small area of the myocardium to avoid mechanical damage to the heart geometry. In addition, the role of endothelin-1 (ET-1) in rat heart with congestive heart failure was critically assessed. Time course initiation experiments were designed by sacrificing the animals at different time intervals and by carrying out physiological, biochemical, histopathological, electron microscopical and immunohistochemical studies. Specific markers of myocardial injury, viz. cardiac troponin-T (cTnT), high sensitivity C-reactive protein, lactate dehydrogenase and fibrinogen were measured at different time points. Serum marker enzymes and activities of lysosomal hydrolases were found to be elevated on the eighth day post-ligation. Histopathological studies demonstrated focal areas showing fibrovascular tissue containing fibroblasts, collagenous ground substance and numerous small capillaries replacing cardiac muscle fibers. Transmission electron micrographs exhibited mitochondrial changes of well-developed irreversible cardiac injury, viz. swelling, disorganization of cristae, appearance of mitochondrial amorphous matrix densities, significant distortion of muscle fibers and distinct disruption of the intercalated discs. Immunoblotting studies confirmed the presence of alpha 2-macroglobulin which supported the inflammatory response. The severity of the CMI was inferred by the measurement of the level of ET-1 in plasma and left ventricle which was significantly higher in the CMI rats than in the sham-operated rats. Immunohistochemical studies at different time intervals showed that there was a significant immunoexpression of ET-1 on the eighth day post-ligation. This study conclusively showed that ligation of left anterior descending artery minimized mortality and ET-1 was expressed during CMI.
大鼠冠状动脉结扎(CAL)诱导的心肌梗死体内模型通常早期死亡率高且诱导率低。本研究调查了白化大鼠慢性心肌梗死(CMI)的发病时间进程,以及通过改进手术技术降低心肌梗死早期死亡率的可能性。CAL通过将缝线穿过左前降支冠状动脉中途周围的心外膜层,包括一小片心肌区域来进行,以避免对心脏几何形状造成机械损伤。此外,还对内皮素-1(ET-1)在充血性心力衰竭大鼠心脏中的作用进行了严格评估。通过在不同时间间隔处死动物并进行生理、生化、组织病理学、电子显微镜和免疫组织化学研究来设计发病时间进程实验。在不同时间点测量心肌损伤的特异性标志物,即心肌肌钙蛋白-T(cTnT)、高敏C反应蛋白、乳酸脱氢酶和纤维蛋白原。发现结扎后第8天血清标志物酶和溶酶体水解酶活性升高。组织病理学研究显示局部区域有含成纤维细胞、胶原基质和许多小毛细血管的纤维血管组织取代心肌纤维。透射电子显微镜照片显示了发育良好的不可逆心脏损伤的线粒体变化,即肿胀、嵴紊乱、线粒体无定形基质密度出现、肌纤维明显扭曲和闰盘明显破坏。免疫印迹研究证实了α2-巨球蛋白的存在,这支持了炎症反应。通过测量血浆和左心室中ET-1的水平推断CMI的严重程度,CMI大鼠中的该水平明显高于假手术大鼠。不同时间间隔的免疫组织化学研究表明,结扎后第8天ET-1有明显的免疫表达。本研究最终表明,左前降支动脉结扎可降低死亡率,且ET-1在CMI期间表达。