Activation of LXR alpha improves cardiac remodeling induced by pulmonary artery hypertension in rats

作者：Gong, Yibo; Yang, Yifeng; Wu, Qin; Gao, Ge; Liu, Yin; Xiong, Yaoyao; Huang, Can; Wu, Sijie^*

来源：Scientific Reports, 2017, 7(1): 6169.

DOI：10.1038/s41598-017-04640-6

• LIVER-X-RECEPTORS
• REVERSE CHOLESTEROL TRANSPORT
• NF-KAPPA-B
• IN-VIVO
• HYPERTROPHY
• PROTECTS
• DYSFUNCTION
• EXPRESSION
• HEART
• ATHEROSCLEROSIS

Inflammatory factors regulated by NF-kappa B play a significant role in PAH and myocardial hypertrophy. LXR activation may inhibit myocardial hypertrophy via suppressing inflammatory pathways; it is unknown whether LXR is also involved in PAH-induced myocardial hypertrophy or remodeling. To further explore the protective effect of LXR in PAH-induced cardiac hypertrophy and remodeling, a PAH model was developed, and T0901317, an agonist of LXR, was used to examine the effect of LXR activation. PAH rats demonstrated obvious cardiac hypertrophy and remodeling in the right ventricle, but significant improvement of cardiac hypertrophy and remodeling was observed in PAH rats treated with T0901317. Through RT-PCR, Western blot and ELISA examination, NF-kappa B,IL-6, TNF-alpha, and iNOS were found to be significantly reduced in PAH rats treated with T0901317 compared to PAH rats treated with DMSO. Apoptosis was also significantly reduced in PAH rats treated with T0901317. Thus, LXR activation may inhibit PAH-induced cardiac hypertrophy and remodeling by inhibiting NF-kappa B-mediated inflammatory pathways.

• 出版日期2017-7-21
• 单位中南大学