Moreno Karyne Garcia Tafarelo, Marques Aline Aparecida Macedo, da Silva Gabriela Pereira, Lourençone Bethânia Rosa, Fortini Clara Soligo, Leite Patrícia Regina Terço, Dos Santos Ariany Carvalho, Souza Roosevelt Isaías Carvalho, da Siva Leila Isabel, Gasparotto Junior Arquimedes
Laboratory of Cardiovascular Pharmacology (LaFAC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados 79825-070, Brazil.
Laboratory of Histopathology, Faculty of Health Sciences, Federal University of Grande Dourados, Dourados 79825-070, Brazil.
Pharmaceuticals (Basel). 2022 Jul 12;15(7):853. doi: 10.3390/ph15070853.
Cardiovascular disease (CVD) is the leading cause of death among non-communicable diseases. There is a lack of valid animal models that mimic associations among multiple cardiovascular risk factors in humans. The present study developed an animal model that uses multiple cardiovascular risk factors-namely, hypertension, hypothyroidism, and a high-fat diet (HFD). Two models of hypertension were used: renovascular hypertension (two-kidney, one clip [2K1C]) and spontaneously hypertensive rats (SHRs). The naive group was composed of normotensive rats. Twelve weeks after surgery to induce renovascular hypertension, rats in the 2K1C and SHR groups underwent thyroidectomy. The HFD was then implemented for 6 weeks. Renal function, serum redox status, biochemical CVD markers, electrocardiographic profile, blood pressure, mesenteric vascular bed reactivity, histopathology, and morphometry were investigated. Both experimental models induced dyslipidemia, renal function impairment, and hepatic steatosis, accompanied by higher levels of different inflammatory markers and serum oxidative stress. These alterations contributed to end-organ damage in all hypertensive rats. Our findings corroborate a viable alternative model that involves multiple cardiovascular risk factors and resembles conditions that are seen in humans. Both models mimicked CVD, but our data show that SHRs exhibit more significant pathophysiological changes.
心血管疾病(CVD)是非传染性疾病中导致死亡的主要原因。目前缺乏能够模拟人类多种心血管危险因素之间关联的有效动物模型。本研究开发了一种利用多种心血管危险因素的动物模型,即高血压、甲状腺功能减退和高脂饮食(HFD)。使用了两种高血压模型:肾血管性高血压(两肾一夹[2K1C])和自发性高血压大鼠(SHR)。单纯组由血压正常的大鼠组成。在诱导肾血管性高血压的手术后12周,2K1C组和SHR组的大鼠接受甲状腺切除术。然后实施6周的高脂饮食。研究了肾功能、血清氧化还原状态、心血管疾病生化标志物、心电图特征、血压、肠系膜血管床反应性、组织病理学和形态学。两种实验模型均诱发了血脂异常、肾功能损害和肝脂肪变性,并伴有不同炎症标志物和血清氧化应激水平升高。这些改变导致了所有高血压大鼠的终末器官损伤。我们的研究结果证实了一种可行的替代模型,该模型涉及多种心血管危险因素,类似于人类中出现的情况。两种模型都模拟了心血管疾病,但我们的数据表明,自发性高血压大鼠表现出更显著的病理生理变化。