Facultad de Medicina, Universidad Autónoma del Estado de Morelos, 62350, Cuernavaca, Morelos, Mexico.
Posgrado en Biología Experimental, Universidad Autónoma Metropolitana-Iztapalapa, 09640, Mexico City, Mexico.
Sci Rep. 2021 Oct 27;11(1):21193. doi: 10.1038/s41598-021-00676-x.
Endothelial dysfunction (ED) is a key factor for the development of cardiovascular diseases. Due to its chronic, life-threatening nature, ED only can be studied experimentally in animal models. Therefore, this work was aimed to characterize a murine model of ED induced by a daily intraperitoneal administration of angiotensin II (AGII) for 10 weeks. Oxidative stress, inflammation, vascular remodeling, hypertension, and damage to various target organs were evaluated in treated animals. The results indicated that a chronic intraperitoneal administration of AGII increases the production of systemic soluble VCAM, ROS and ICAM-1 expression, and the production of TNFα, IL1β, IL17A, IL4, TGFβ, and IL10 in the kidney, as well as blood pressure levels; it also promotes vascular remodeling and induces non-alcoholic fatty liver disease, glomerulosclerosis, and proliferative retinopathy. Therefore, the model herein proposed can be a representative model for ED; additionally, it is easy to implement, safe, rapid, and inexpensive.
内皮功能障碍 (ED) 是心血管疾病发展的关键因素。由于其慢性、危及生命的性质,ED 只能在动物模型中进行实验研究。因此,本工作旨在表征一种通过每日腹腔内给予血管紧张素 II (AGII) 10 周诱导 ED 的小鼠模型。在治疗动物中评估了氧化应激、炎症、血管重塑、高血压以及各种靶器官损伤。结果表明,慢性腹腔内给予 AGII 会增加全身可溶性 VCAM、ROS 和 ICAM-1 的表达,以及肾脏中 TNFα、IL1β、IL17A、IL4、TGFβ 和 IL10 的产生,并升高血压水平;还会促进血管重塑,并诱导非酒精性脂肪肝、肾小球硬化和增殖性视网膜病变。因此,本文提出的模型可以作为 ED 的代表性模型;此外,该模型易于实施、安全、快速且廉价。