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Tacrolimus-induced hypertension and nephrotoxicity in Fawn-Hooded rats are attenuated by dual inhibition of renin-angiotensin system
L. Hošková, I. Málek, J. Kautzner, E. Honsová, RP. van Dokkum, Z. Husková, A. Vojtíšková, S. Varcabová, L. Cervenka, L. Kopkan,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NT11262
MZ0
CEP - Centrální evidence projektů
NT12171
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Zdroj
Zdroj
NLK
Medline Complete (EBSCOhost)
od 2009-01-01 do 2015-11-30
PubMed
24718302
DOI
10.1038/hr.2014.79
Knihovny.cz E-zdroje
- MeSH
- akutní poškození ledvin chemicky indukované prevence a kontrola MeSH
- beta blokátory farmakologie MeSH
- blokátory kalciových kanálů farmakologie MeSH
- blokátory receptorů AT1 pro angiotensin II farmakologie MeSH
- dieta MeSH
- imunosupresiva antagonisté a inhibitory toxicita MeSH
- inhibitory ACE farmakologie MeSH
- kalcineurin účinky léků MeSH
- krysa rodu rattus MeSH
- renin-angiotensin systém účinky léků MeSH
- takrolimus antagonisté a inhibitory toxicita MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Chronic immunosuppressive therapy is often complicated by the development of both arterial hypertension and renal dysfunction. The principal aim of this study was to assess the effects of dual inhibition of renin-angiotensin system (RAS) and other antihypertensive treatment on blood pressure and renal function in normotensive and hypertensive Fawn-Hooded (FH) strains during chronic calcineurin inhibitor (CNI) administration. Combinations of perindopril (5 mg kg(-1) per day) and losartan (50 mg kg(-1) per day) or amlodipine (6 mg kg(-1) per day) and metoprolol (80 mg kg(-1) per day) were administered to normotensive (FHL) and hypertensive (FHH) rats, fed with diet containing tacrolimus (Tac; 12 mg kg(-1) per day). Tac-induced arterial hypertension in both animal strains (FHL: 151±4; FHH: 198±6 mm Hg) was prevented by dual RAS inhibition (FHL: 132±3 mm Hg, P<0.05; FHH: 153±3 mm Hg, P<0.05) as well as by a combination of amlodipine and metoprolol (FHL: 136±3 mm Hg, P<0.05; FHH: 166±4 mm Hg, P<0.05). However, significant nephroprotection was observed only in animals on dual RAS inhibition where albuminuria was reduced in both FHL (51.1±3.9 vs. 68.3±4.5 μg per day; P<0.05) and FHH rats (13.1±0.3 vs. 18.8±0.7 mg per day; P<0.05). We also found Tac-induced enhancement in renal angiotensin II activity that was significantly reduced by dual RAS inhibition in both FHL (63.5±3.2 vs. 23.1±3.0 fmol g(-1)) and FHH (79.8±8.5 vs. 32.2±5.8 fmol g(-1)). In addition, histological analysis revealed that RAS inhibition noticeably diminished glomerulosclerosis and tubulo-interstitial injury. This study indicates that dual blockade of RAS significantly attenuates Tac-induced arterial hypertension and nephrotoxicity in FH rats and further supports the notion that RAS inhibitors display efficient renoprotective properties during CNI treatment.
Department of Cardiology Institute for Clinical and Experimental Medicine Prague Czech Republic
Department of Clinical Pharmacology University Medical Center Groningen Groningen The Netherlands
Citace poskytuje Crossref.org
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