Uraemic Cardiomyopathy in Different Mouse Models

被引:9
作者
Chen, Cheng [1 ,2 ]
Xie, Caidie [1 ]
Wu, Hanzhang [1 ]
Wu, Lin [1 ]
Zhu, Jingfeng [1 ]
Mao, Huijuan [1 ]
Xing, Changying [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Jiangsu Prov Hosp, Dept Nephrol, Nanjing, Peoples R China
[2] Yangzhou Polytech Coll, Dept Med Sci, Yangzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
uraemic cardiomyopathy; mouse models; surgical method; adenine; GDF-15; FGF-23; CHRONIC KIDNEY-DISEASE; LEFT-VENTRICULAR HYPERTROPHY; GROWTH-FACTOR; 23; HEART-FAILURE; KLOTHO; PATHOGENESIS; NEPHRECTOMY; DYSFUNCTION; PROGRESSION; PREVALENCE;
D O I
10.3389/fmed.2021.690517
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Uraemic cardiomyopathy (UCM) is one of the most common complications in chronic kidney disease (CKD). Our aim was to compare characteristics of various UCM mouse models. Mice were assigned to the following groups: the pole ligation group, 5/6 nephrectomy group (5/6Nx), uninephrectomy plus contralateral ischemia followed by reperfusion group (IR), adenine group, and sham group. Mice were sacrificed at 4, 8, and 16 weeks after surgery in the pole ligation, 5/6Nx, and IR groups, respectively. In the adenine group, mice were sacrificed at 16 weeks after the adenine diet. The structure and function of the heart and the expression of fibroblast growth factor 23 (FGF-23) and growth differentiation factor 15 (GDF-15) in hearts were assessed. The mortality in the 5/6 Nx group was significantly higher than that in the pole ligation, IR, and adenine groups. Echocardiogram and histological examination showed cardiac hypertrophy in the adenine,5/6Nx, ligation group, and IR group. In addition, cardiac fibrosis occurred in all CKD modeling groups. Interestingly, cardiac fibrosis was more serious in the IR and adenine groups. FGF-23 expression in sham mice was similar to that in modeling groups; however, the GDF-15 level was decreased in modeling groups. Our results suggest that the four models of UCM show different phenotypical features, molding time and mortality. GDF-15 expression in the hearts of UCM mice was downregulated compared with sham group mice.
引用
收藏
页数:12
相关论文
共 41 条
[11]   Fibroblast Growth Factor 23 and Left Ventricular Hypertrophy in Chronic Kidney Disease [J].
Gutierrez, Orlando M. ;
Januzzi, James L. ;
Isakova, Tamara ;
Laliberte, Karen ;
Smith, Kelsey ;
Collerone, Gina ;
Sarwar, Ammar ;
Hoffmann, Udo ;
Coglianese, Erin ;
Christenson, Robert ;
Wang, Thomas J. ;
deFilippi, Christopher ;
Wolf, Myles .
CIRCULATION, 2009, 119 (19) :2545-2552
[12]   International comparison of the relationship of chronic kidney disease prevalence and ESRD risk [J].
Hallan, Stein I. ;
Coresh, Josef ;
Astor, Brad C. ;
Asberg, Arne ;
Powe, Neil R. ;
Romundstad, Solfrid ;
Hallan, Hans A. ;
Lydersen, Stian ;
Holmen, Jostein .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (08) :2275-2284
[13]   Recombinant α-Klotho may be prophylactic and therapeutic for acute to chronic kidney disease progression and uremic cardiomyopathy [J].
Hu, Ming Chang ;
Shi, Mingjun ;
Gillings, Nancy ;
Flores, Brianna ;
Takahashi, Masaya ;
Kuro-o, Makoto ;
Moe, Orson W. .
KIDNEY INTERNATIONAL, 2017, 91 (05) :1104-1114
[14]   Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease [J].
Isakova, Tamara ;
Wahl, Patricia ;
Vargas, Gabriela S. ;
Gutierrez, Orlando M. ;
Scialla, Julia ;
Xie, Huiliang ;
Appleby, Dina ;
Nessel, Lisa ;
Bellovich, Keith ;
Chen, Jing ;
Hamm, Lee ;
Gadegbeku, Crystal ;
Horwitz, Edward ;
Townsend, Raymond R. ;
Anderson, Cheryl A. M. ;
Lash, James P. ;
Hsu, Chi-yuan ;
Leonard, Mary B. ;
Wolf, Myles .
KIDNEY INTERNATIONAL, 2011, 79 (12) :1370-1378
[15]  
Jonathan P., 2020, J AM HEART ASSOC, V9, DOI [10.1161/JAHA.119.014566, DOI 10.1161/JAHA.119.014566]
[16]   Effect of chronic renal failure on cardiac contractile function, calcium cycling, and gene expression of proteins important for calcium homeostasis in the rat [J].
Kennedy, D ;
Omran, M ;
Periyasamy, SM ;
Nadoor, J ;
Priyadarshi, A ;
Willey, JC ;
Malhotra, D ;
Xie, ZJ ;
Shapiro, JI .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (01) :90-97
[17]   Partial nephrectomy as a model for uremic cardiomyopathy in the mouse [J].
Kennedy, David J. ;
Elkareh, Jihad ;
Shidyak, Amjad ;
Shapiro, Anna P. ;
Smaili, Sleiman ;
Mutgi, Krishna ;
Gupta, Shalini ;
Tian, Jiang ;
Morgan, Eric ;
Khouri, Samer ;
Cooper, Christopher J. ;
Periyasamy, Sankaridrug M. ;
Xie, Zijian ;
Malhotra, Deepak ;
Fedorova, Olga V. ;
Bagrov, Alexei Y. ;
Shapiro, Joseph I. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2008, 294 (02) :F450-F454
[18]   Central role for the cardiotonic steroid marinobufagenin in the pathogenesis of experimental uremic cardiomyopathy [J].
Kennedy, DJ ;
Vetteth, S ;
Periyasamy, SM ;
Kanj, M ;
Fedorova, L ;
Khouri, S ;
Kahaleh, MB ;
Xie, ZJ ;
Malhotra, D ;
Kolodkin, NI ;
Lakatta, EG ;
Fedorova, OV ;
Bagrov, AY ;
Shapiro, JI .
HYPERTENSION, 2006, 47 (03) :488-495
[19]   A novel model of reno-cardiac syndrome in the C57BL/ 6 mouse strain [J].
Kieswich, Julius E. ;
Chen, Jianmin ;
Alliouachene, Samira ;
Caton, Paul W. ;
McCafferty, Kieran ;
Thiemermann, Christoph ;
Yaqoob, Muhammad M. .
BMC NEPHROLOGY, 2018, 19
[20]   Novel biomarkers in human terminal heart failure and under mechanical circulatory support [J].
Kramer, Frank ;
Milting, Hendrik .
BIOMARKERS, 2011, 16 :S31-S41