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Mycophenolate mofetil prevents arteriolopathy and renal injury in subtotal ablation despite persistent hypertension.
- Source :
-
Kidney international [Kidney Int] 2003 Mar; Vol. 63 (3), pp. 994-1002. - Publication Year :
- 2003
-
Abstract
- Background: Although renal protective effect of interrupting the inflammatory process is well established, it is still controversial if it also prevents the glomerular hemodynamic disturbances that initiate renal injury. We investigated the effects of suppressing inflammation with mycophenolate mofetil (MMF) on glomerular hemodynamics, arteriolar structural changes, and renal histologic injury in rats with subtotal renal ablation<br />Methods: Micropuncture studies were performed 30 days after 5/6 nephrectomy in rats untreated and treated with MMF (30 mg/kg/day). Renal histology, immunohistochemistry for lymphocytes, macrophages and inducible nitric oxide synthase (iNOS) expression, as well as afferent arteriolar (AA) morphometry was evaluated.<br />Results: Renal ablation significantly increased proteinuria (6.8 to 82.7 mg/day), mean arterial pressure (MAP) (120 to 166 mm Hg), single-nephron glomerular filtration rate (SNGFR) (34.8 to 56.3 nL/min), glomerular plasma flow (QA) (117.7 to 246.9 nL/min), and glomerular capillary pressure (PGC) (48.9 to 61.0 mm Hg). Afferent resistance (AR), efferent resistance, and ultrafiltration coefficient remained unchanged. Despite persisting arterial hypertension (152 mm Hg), MMF prevented proteinuria (13.3 mg/day), and significantly reduced SNGFR (44.4 nL/min), PGC (49.1 mm Hg), and QA (163.2 nL/min) due to a rise in AR (3.13 vs. 2.18 1010 dyn/sec/cm-5). Glomerular sclerosis, tubulointerstitial damage, lymphocyte and macrophage infiltration, and iNOS expression were significantly reduced by MMF, in addition hypertrophy of AA resistance evaluated by the media/lumen ratio was prevented (P < 0.001).<br />Conclusions: Reduction in proteinuria, SNGFR, QA, and PGC, despite elevated MAP, indicate preservation of AA function. These results suggest that inflammation associated arteriolopathy of AA contributes to glomerular hemodynamic disturbances that participate in the progression of renal disease.
- Subjects :
- Animals
Arterioles pathology
Hypertension, Renal pathology
Kidney blood supply
Male
Nephrectomy
Nephritis drug therapy
Nephritis pathology
Nephritis prevention & control
Proteinuria pathology
Proteinuria prevention & control
Rats
Rats, Sprague-Dawley
Renal Circulation
Anti-Inflammatory Agents, Non-Steroidal pharmacology
Hypertension, Renal drug therapy
Mycophenolic Acid analogs & derivatives
Mycophenolic Acid pharmacology
Proteinuria drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 0085-2538
- Volume :
- 63
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Kidney international
- Publication Type :
- Academic Journal
- Accession number :
- 12631080
- Full Text :
- https://doi.org/10.1046/j.1523-1755.2003.00811.x