Salerno Nadia, Scalise Mariangela, Marino Fabiola, Filardo Andrea, Chiefalo Antonio, Panuccio Giuseppe, Torella Michele, De Angelis Antonella, De Rosa Salvatore, Ellison-Hughes Georgina M, Urbanek Konrad, Viglietto Giuseppe, Torella Daniele, Cianflone Eleonora
Department of Experimental and Clinical Medicine, Magna Graecia University, 88100 Catanzaro, Italy.
Department of Medical and Surgical Sciences, Magna Graecia University, 88100 Catanzaro, Italy.
J Cardiovasc Dev Dis. 2023 May 23;10(6):225. doi: 10.3390/jcdd10060225.
Appropriate dilated cardiomyopathy (DCM) animal models are highly desirable considering the pathophysiological and clinical heterogeneity of DCM. Genetically modified mice are the most widely and intensively utilized research animals for DCM. However, to translate discoveries from basic science into new and personalized medical applications, research in non-genetically based DCM models remains a key issue. Here, we characterized a mouse model of non-ischemic DCM induced by a stepwise pharmacologic regime of Isoproterenol (ISO) high dose bolus followed by a low dose systemic injection of the chemotherapy agent, 5-Fluorouracil (5-FU). C57BL/6J mice were injected with ISO and, 3 days after, were randomly assigned to saline or 5-FU. Echocardiography and a strain analysis show that ISO + 5FU in mice induces progressive left ventricular (LV) dilation and reduced systolic function, along with diastolic dysfunction and a persistent global cardiac contractility depression through 56 days. While mice treated with ISO alone recover anatomically and functionally, ISO + 5-FU causes persistent cardiomyocyte death, ensuing in cardiomyocyte hypertrophy through 56 days. ISO + 5-FU-dependent damage was accompanied by significant myocardial disarray and fibrosis along with exaggerated oxidative stress, tissue inflammation and premature cell senescence accumulation. In conclusions, a combination of ISO + 5FU produces anatomical, histological and functional cardiac alterations typical of DCM, representing a widely available, affordable, and reproducible mouse model of this cardiomyopathy.
考虑到扩张型心肌病(DCM)的病理生理和临床异质性,合适的DCM动物模型非常必要。基因改造小鼠是用于DCM研究的最广泛且深入使用的实验动物。然而,为了将基础科学的发现转化为新的个性化医学应用,基于非基因的DCM模型的研究仍然是一个关键问题。在此,我们描述了一种非缺血性DCM小鼠模型,该模型通过异丙肾上腺素(ISO)高剂量推注后低剂量全身注射化疗药物5-氟尿嘧啶(5-FU)的逐步药理学方案诱导。将C57BL/6J小鼠注射ISO,3天后随机分为生理盐水组或5-FU组。超声心动图和应变分析表明,小鼠体内的ISO + 5FU会导致进行性左心室(LV)扩张和收缩功能降低,同时伴有舒张功能障碍以及持续至56天的整体心脏收缩力下降。虽然单独用ISO治疗的小鼠在解剖学和功能上可恢复,但ISO + 5-FU会导致持续的心肌细胞死亡,在56天内导致心肌细胞肥大。ISO + 5-FU依赖性损伤伴随着明显的心肌排列紊乱和纤维化,以及过度的氧化应激、组织炎症和过早的细胞衰老积累。总之,ISO + 5FU的组合产生了DCM典型的解剖学、组织学和功能性心脏改变,代表了一种广泛可用、经济实惠且可重复的这种心肌病小鼠模型。