| Title | Mineralocorticoid receptor blockade and calcium channel blockade have different renoprotective effects on glomerular and interstitial injury in rats. | | Author(s) | Du J, Fan YY, Hitomi H, Kiyomoto H, Kimura S, Kong CZ, Noma T, Kohno M, Nishiyama A, Nakano D | | Institution | Kagawa University. | | Source | Am J Physiol Renal Physiol 2009 Jun 17. | | Abstract | We hypothesized that combination treatment with the mineralocorticoid receptor antagonist, eplerenone, and the calcium channel blocker, amlodipine, elicits better renoprotective effects than monotherapy with either drug, via different mechanisms in Dahl salt-sensitive (DS) hypertensive rats. DS rats were fed a high salt diet (4% NaCl) for 10 weeks and were treated with vehicle (n=12), eplerenone (50 mg/kg/day, p.o., n=12), amlodipine (3 mg/kg/day, p.o., n=12), or eplerenone plus amlodipine (n=12), after 2 weeks' salt feeding. Vehicle-treated DS rats developed proteinuria, which was attenuated by eplerenone or amlodipine. Interestingly, eplerenone attenuated the glomerulosclerosis and podocyte injury, but amlodipine did not. Conversely, treatment with amlodipine markedly improved the interstitial fibrosis, while the effect of eplerenone was minimal. Combination treatment markedly improved the proteinuria, glomerulosclerosis, podocyte injury and interstitial fibrosis in DS rats. Renal hypoxia estimated by pimonidazole, vascular endothelial growth factor expression and density of peritubular endothelial cells was exacerbated by salt feeding. Amlodipine, either as monotherapy or in combination, ameliorated the renal hypoxia, whereas eplerenone treatment had no effect. In conclusion, both eplerenone and amlodipine attenuated renal injuries in high salt-fed DS rats, but the targets for renoprotection differed between these two drugs, with eplerenone predominantly acting on glomeruli and amlodipine acting on interstitium. Combination of eplerenone and amlodipine improved the renal injury more effectively than either monotherapy in high salt-fed DS rats, presumably by achieving their own renoprotective effects. Key words: salt-sensitive hypertension, hypoxia, glomerular injury, interstitial fibrosis. | | Language | ENG | | Pub Type(s) | JOURNAL ARTICLE
| | PubMed ID | 19535572 |
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