Zhao Wei, Yin Yane, Cao Huiling, Wang Yandong
Department of Neonatology, Weifang People's Hospital, Weifang 261041, Shandong, China.
Department of Pediatrics, Weifang People's Hospital, Weifang 261041, Shandong, China.
Cardiol Res Pract. 2021 Jun 2;2021:8840698. doi: 10.1155/2021/8840698. eCollection 2021.
Endothelial dysfunction commonly occurs in obese children and adolescents, leading to an increased risk of cardiovascular diseases. Exercise has significant protective effects against endothelial dysfunction through regulating some noncoding RNAs. This study aimed to investigate the relationship of long noncoding RNA MALAT1 and microRNA-320a (miR-320a) with the exercise-induced improvement of endothelial dysfunction in obese children and adolescents.
Sixty obese children and adolescents were included in this study, including 40 cases that received 12-week exercise training and 20 cases that received only diet control. The anthropometric and blood indices before and after exercise were recorded and compared, and the endothelial dysfunction was evaluated by examining the levels of markers, including VCAM-1, ICAM-1, and E-selectin, using an ELISA assay. The expression levels of noncoding RNAs were assessed using real-time quantitative PCR, and their correlation with patients' recorded indices and endothelial dysfunction markers was analyzed.
The 12-week exercise training significantly decreased the levels of VCAM-1, ICAM-1, and E-selectin and could inhibit MALAT1 but promote miR-320a expression in obese children and adolescents. The expression of MALAT1 and miR-320a was correlated with the changes in the anthropometric and blood indices of obese children and adolescents, and their correlations with endothelial dysfunction markers were obtained.
All the data revealed that exercise has significantly protective effects against endothelial dysfunction and can regulate the expression of the MALAT1/miR-320a axis. MALAT1 and miR-320a were correlated with endothelial dysfunction markers, indicating that the MALAT1/miR-320a axis may be related with the alleviating effects of exercise on endothelial function in obese children and adolescents.
内皮功能障碍常见于肥胖儿童和青少年,会导致心血管疾病风险增加。运动通过调节一些非编码RNA对内皮功能障碍具有显著的保护作用。本研究旨在探讨长链非编码RNA MALAT1和微小RNA-320a(miR-320a)与运动诱导肥胖儿童和青少年内皮功能障碍改善之间的关系。
本研究纳入60名肥胖儿童和青少年,其中40例接受为期12周的运动训练,20例仅接受饮食控制。记录并比较运动前后的人体测量和血液指标,采用酶联免疫吸附测定法检测包括血管细胞黏附分子-1(VCAM-1)、细胞间黏附分子-1(ICAM-1)和E-选择素在内的标志物水平,评估内皮功能障碍。采用实时定量聚合酶链反应评估非编码RNA的表达水平,并分析其与患者记录指标及内皮功能障碍标志物的相关性。
为期12周的运动训练显著降低了肥胖儿童和青少年的VCAM-1、ICAM-1和E-选择素水平,可抑制MALAT1表达,但促进miR-320a表达。MALAT1和miR-320a的表达与肥胖儿童和青少年人体测量及血液指标的变化相关,并得出了它们与内皮功能障碍标志物的相关性。
所有数据表明,运动对内皮功能障碍具有显著保护作用,并可调节MALAT1/miR-320a轴的表达。MALAT1和miR-320a与内皮功能障碍标志物相关,表明MALAT1/miR-320a轴可能与运动对肥胖儿童和青少年内皮功能的改善作用有关。