Aliskiren attenuates proteinuria in mice with lupus nephritis by a blood pressure-independent mechanism

被引:12
|
作者
Yen, T-H [1 ,2 ]
Yang, H-Y [1 ,2 ]
Yeh, Y-H [2 ,3 ]
Chu, P-H [2 ,3 ]
Wen, C-J [4 ]
Fu, J-F [5 ]
Wang, I-K [6 ]
Liang, C-C [6 ]
Chang, C-T [6 ]
Chen, K-H [1 ,2 ]
Tian, Y-C [1 ,2 ]
Hung, C-C [1 ,2 ]
Lin, J-L [1 ,2 ]
Yang, C-W [1 ,2 ]
机构
[1] Chang Gung Mem Hosp, Dept Nephrol, Kidney Res Ctr, Taipei 105, Taiwan
[2] Chang Gung Univ, Coll Med, Tao Yuan, Taiwan
[3] Chang Gung Mem Hosp, Cardiovasc Div 1, Taipei 105, Taiwan
[4] Chang Gung Mem Hosp, Mol Imaging Ctr, Taipei 105, Taiwan
[5] Chang Gung Mem Hosp, Dept Med Res, Taipei 105, Taiwan
[6] China Med Univ, Coll Med, Taichung, Taiwan
关键词
Direct renin inhibitor; aliskiren; lupus nephritis; blood pressure; proteinuria; non-invasion in vivo imaging system; UNILATERAL URETERAL OBSTRUCTION; RENIN INHIBITOR ALISKIREN; RENAL FIBROSIS; EXPRESSION; CAPTOPRIL; DISEASE; DAMAGE; CELLS;
D O I
10.1177/0961203312471871
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study revealed that low-dose aliskiren treatment could attenuate proteinuria by interrupting the renin-angiotensin system in mice with lupus nephritis, and the beneficial effect was beyond blood pressure control. An in and ex vivo fluorescence imaging (using a non-invasion in vivo imaging system) showed intense labeling of renin in the kidneys of female MRL/lpr mice. In the study, Alzet mini-osmotic pumps were implanted into 6-week-old female MRL/lpr mice. Pumps were filled with either phosphate-buffered saline or a solution of aliskiren dissolved in phosphate-buffered saline (20 mg/kg/day) and replaced at 28-day intervals. Mice were sacrificed at four and eight weeks. To label cells for DNA synthesis, bromodeoxyuridine (BrdU) (50 mg/kg) was injected intraperitoneally an hour prior to sacrifice. The level of renin inhibition was adequate, as aliskiren-treated mice demonstrated higher renal renin mRNA expression than controls (p < 0.05). Although there were no significant differences in the systolic blood pressure (control versus aliskiren-treated: 127.20 +/- 4.44 mmHg versus 103.80 +/- 7.40 mmHg, p > 0.05) and heart rate (control versus aliskiren-treated: 680.50 +/- 11.71 versus 647.80 +/- 13.90, p > 0.05) of both groups after eight weeks, there was significant reduction of inflammatory cytokines (transforming growth factor-beta1, regulated on activation normal T cell expressed, monocyte chemoattractant protein-1 and osteopontin, p < 0.05), reduction of innate immunity (toll-like receptor 7, p < 0.05), as well as a reduction of glomerular proliferation and inflammation (BrdU-, CD45-, CD3- and F4/80-positive glomerular cells, p < 0.01) after aliskiren infusion, which might translate into an improvement in proteinuria (control versus aliskiren-treated: 493.7 versus 843.7 mg/g, p < 0.01) or weight gain (control versus aliskiren-treated: 5.65 +/- 1.61 versus 8.67 +/- 0.97%, p < 0.05). Lupus (2013) 22, 180-189.
引用
收藏
页码:180 / 189
页数:10
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