Universitas Gadjah Mada, Public Health, and Nursing, Faculty of Medicine, Department of Anatomy, Yogyakarta, Indonesia.
Universitas Gadjah Mada, Public Health, and Nursing, Faculty of Medicine, Yogyakarta, Indonesia.
Med J Malaysia. 2022 Jul;77(Suppl 1):23-27.
Obesity alters several metabolic activities, subsequently leading to the development of cardiovascular diseases. The insulin resistance-induced obesity stimulates vasodilatation and vasoconstriction imbalance, which ends up in cardiac vascular remodeling. Therefore, we aimed to investigate the effect of obesity in cardiac diseases with a focus on inflammatory mediators associated with endothelial dysfunction.
Rats (3 months old, weighing 200 g) were divided into control (n=6) and the obese groups, which included rats fed on a high-fat diet (HFD, n=6 in each subgroup) for 1 month (OB1), 2 months (OB2), and 4 months (OB4). Then, the rats were sacrificed, and their hearts were harvested for histological quantification as well as the quantification of the mRNA expression of inflammatory mediators, eNOS, and ppET-1 by reverse transcriptasepolymerase chain reaction (RT-PCR). Sirius Red staining was performed to assess vascular remodeling, while immunohistochemistry of CD68 was performed to assess the localization of macrophage.
HFD-induced obesity was significantly manifested in the obese groups relative to that in the control group. It was followed by an increase in the mRNA expression of inflammatory mediators in the obese groups when compared to that in the control group. Long-term obesity promoted vascular remodeling, which was noted in the OB4 group, along with downregulation of the eNOS mRNA expression and the upregulation of the ppET-1 mRNA expression.
Obesity associated with inflammation and vascular remodeling in the heart.
肥胖改变了多种代谢活动,继而导致心血管疾病的发生。胰岛素抵抗引起的肥胖会刺激血管舒张和收缩失衡,最终导致心脏血管重塑。因此,我们旨在研究肥胖对心脏病的影响,重点关注与内皮功能障碍相关的炎症介质。
将 3 个月大、体重 200 克的大鼠分为对照组(n=6)和肥胖组,肥胖组再分为高脂饮食喂养 1 个月(OB1,每组 n=6)、2 个月(OB2)和 4 个月(OB4)的大鼠。然后处死大鼠,取心脏进行组织学定量以及通过逆转录聚合酶链反应(RT-PCR)定量炎症介质、eNOS 和 ppET-1 的 mRNA 表达。进行天狼星红染色以评估血管重塑,并用 CD68 免疫组化评估巨噬细胞的定位。
与对照组相比,高脂饮食诱导的肥胖在肥胖组中表现明显。与对照组相比,肥胖组的炎症介质 mRNA 表达增加。长期肥胖导致血管重塑,在 OB4 组中观察到,同时 eNOS mRNA 表达下调和 ppET-1 mRNA 表达上调。
肥胖与心脏中的炎症和血管重塑有关。