Evolocumab prevents atrial fibrillation in rheumatoid arthritis rats through restraint of PCSK9 induced atrial remodeling

被引:3
作者
Han, Xuejie [1 ]
Gao, Yunlong [1 ]
He, Meijiao [1 ]
Luo, Yingchun [1 ]
Wei, Ying [1 ]
Duan, Yu [1 ]
Zhang, Song [1 ]
Yu, Hui [1 ]
Kan, Jiuxu [1 ]
Hou, Te [1 ]
Zhang, Yun [1 ]
Li, Yue [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Cardiol, Youzheng St 23, Harbin 150001, Peoples R China
[2] Harbin Med Univ, NHC Key Lab Cell Translat, Harbin 150001, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Key Lab Hepatosplen Surg, Minist Educ, Harbin 150001, Peoples R China
[4] Harbin Med Univ, Key Lab Cardiac Dis & Heart Failure, Harbin 150001, Peoples R China
[5] Heilongjiang Key Lab Metab Disorder & Canc Related, Harbin 150081, Peoples R China
[6] Heilongjiang Acad Med Sci, Inst Metab Dis, Harbin, Peoples R China
基金
中国国家自然科学基金;
关键词
Rheumatoid arthritis; Atrial fibrillation; PCSK9; Evolocumab; INHIBITION; HEART;
D O I
10.1016/j.jare.2023.09.007
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Proprotein convertase subtilisin/kexin type 9 (PCSK9) is implicated in the pathogenesis and progression of autoimmune disease. Patients with rheumatoid arthritis (RA) are at high risk of developing atrial fibrillation (AF), while whether PCSK9 is involved in the onset of AF among RA patients remains unclear. Objectives: To explore the role of PCSK9 in the occurrence of AF in RA patients and decipher the underlying mechanism. Methods: We established a rat model of collagen-induced arthritis (CIA) by immunization with type II collagen in Freund's incomplete adjuvant. Atrial electrophysiological test was used to evaluate AF susceptibility. We performed a clinical study to examine the correlation between PCSK9 level and AF, which recruited healthy control, RA patients and RA patients complicated with AF. Evolocumab (a monoclonal antibody of PCSK9) is administered via intraperitoneal injection in CIA rats to assess the role of PCSK9 in RA-related AF. LPS-RS (LPS inhibitor), clodronate liposomes (depletion of macrophages), and cell co- culture model were used to dissect the mechanism underlying PCSK9 promotes AF. Results: AF inducibility and duration were higher in CIA rats, accompanied by elevated plasma and atrial PCSK9. Interestingly, compared with healthy control subjects, patients with RA showed an increase in PCSK9, and the PCSK9 is much higher in RA patients complicated with AF. The level of PCSK9 was independently associated with AF risk in RA patients. In the in vivo experiment, evolocumab reduced AF susceptibility, and ameliorated atrial structural remodeling of CIA rats. Mechanistically, augmented LPS in CIA rats led to an increase in PCSK9, which exacerbated fibrosis of cardiac fibroblasts and apoptosis of cardiac myocytes by enhancement of M1 macrophages polarization and inflammation, thereby contributing to AF. Conclusion: This study suggests that elevated PCSK9 causes atrial structural remodeling by enhancement of M1 macrophages polarization in atria, and evolocumab can effectively protects CIA rats from AF. (c) 2024 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:211 / 221
页数:11
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