Ischemia/Reperfusion of Unilateral Kidney Exaggerates Aging-Induced Damage to the Heart and Contralateral Kidney

被引:8
|
作者
Kato, Junichiro [1 ,3 ]
Nakayama, Masaaki [1 ,2 ,4 ]
Zhu, Wan-Jun [1 ,4 ]
Yokoo, Takashi [3 ]
Ito, Sadayoshi [1 ,2 ]
机构
[1] Tohoku Univ, Grad Sch Med, Res Div CKD & Dialysis, Sendai, Miyagi 980, Japan
[2] Tohoku Univ, Grad Sch Med, Ctr Adv Integrated Renal Sci, Sendai, Miyagi 980, Japan
[3] Jikei Univ, Sch Med, Dept Kidney & Hypertens, Tokyo, Japan
[4] Fukushima Med Univ, Sch Med, Dept Kidney & Hypertens, Fukushima, Japan
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2014年 / 126卷 / 04期
关键词
Inflammation; Cardiovascular diseases; Macrophage infiltration; Fibrosis; ACUTE-RENAL-FAILURE; REGENERATIVE CAPACITY; INJURY; ISCHEMIA; IMPACT; PROLIFERATION; REPERFUSION; EXPRESSION; MORTALITY; OUTCOMES;
D O I
10.1159/000362555
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aims: We aimed to determine the impact of aging on ischemic acute kidney injury, especially in terms of the pathological mechanisms of kidney and heart crosstalk. Method: The effects of 45 min of unilateral ischemic reperfusion (IR) of the renal artery on the contralateral kidney and heart were histologically assessed in 7- and 40-week-old SD rats after 7 days. Results: Glomerular sclerosis, interstitial fibrosis and numbers of ED1 cells were significantly increased in the contralateral kidneys of the 40-, but not the 7-week-old rats. The numbers of ED1 cells in the heart significantly and similarly increased in both groups, but reactive fibrosis after IR was significant only in the 40-week-old rats. The exaggerated profibrotic response induced by aging seemed to be closely associated with the increased number of ED1 cells in the affected area. Conclusion: Aging could play a major role in exaggerating the pathological processes of inflammation to fibrosis in remote organs including the heart and the non-ischemic kidney after IR stimulation of the unilateral kidney. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:183 / 190
页数:8
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