4.3 Article

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

Journal

LUPUS
Volume 22, Issue 2, Pages 180-189

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/0961203312471871

Keywords

Direct renin inhibitor; aliskiren; lupus nephritis; blood pressure; proteinuria; non-invasion in vivo imaging system

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Funding

  1. Chang Gung Memorial Hospital [CMRP G3A0321, G3A0322, G300191]
  2. Taiwan Society of Nephrology Renin Academy Project

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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.

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