Nichtova Zuzana, Novotova Marta, Kralova Eva, Stankovicova Tatiana
Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Vlárska 5, 833 34 Bratislava, Slovak Republic.
Gen Physiol Biophys. 2012 Jun;31(2):141-51. doi: 10.4149/gpb_2012_015.
The animal models of myocardial injury induced by systemic β-adrenergic receptor agonist administration represent an experimental approach of persisting interest. These models were found useful especially for studies of structural and functional adaptation of myocardium during the progression of cardiac adaptive response towards maladaptive hypertrophy and insufficiency. The pathological alterations induced by isoproterenol (ISO) do not develop evenly. The ISO models may contribute effectively to understanding of pathologies in signal transduction, energetics, excitability and contractility that may contribute concomitantly to cardiac dysfunction and heart failure. In this minireview we focused on the alterations in general characteristics and heart function as well as on the morphological changes of cardiomyocytes developed during ISO administration. The morphological alterations within the cellular macro- and microdomains correspond to the electrical remodelling and contractile dysfunction of ventricular myocardium that could be used to identify pathological changes ranging from hypertrophy to failing heart.
通过全身给予β-肾上腺素能受体激动剂诱导心肌损伤的动物模型是一种一直备受关注的实验方法。这些模型被发现特别适用于研究心肌在从适应性反应向适应不良性肥大和功能不全进展过程中的结构和功能适应性。异丙肾上腺素(ISO)诱导的病理改变并非均匀发生。ISO模型可能有助于有效理解信号转导、能量代谢、兴奋性和收缩性方面的病理变化,这些变化可能同时导致心脏功能障碍和心力衰竭。在本综述中,我们重点关注了ISO给药期间心肌细胞的一般特征和心脏功能变化以及形态学改变。细胞宏观和微观结构域内的形态学改变与心室心肌的电重构和收缩功能障碍相对应,可用于识别从肥大到心力衰竭的病理变化。