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dc.contributor.authorHusain, Kazim
dc.contributor.authorSuárez- Martínez, Edu B.
dc.contributor.authorIsidro, Angel
dc.contributor.authorHernandez, Wilfredo
dc.contributor.authorFerder, Leon
dc.date.accessioned2017-05-24T21:58:48Z
dc.date.available2017-05-24T21:58:48Z
dc.date.issued2015-08-26
dc.identifier.citationWorld Journal of Biological Chemistry Volume: 6 Issue: 3 Pages: 240 - 248 August 2015en_US
dc.identifier.urihttp://www.wjgnet.com/1949-8454/abstract/v6/i3/240.htm
dc.identifier.urihttp://hdl.handle.net/11721/1602
dc.description.abstractAIM: To investigate the protective effect of paricalcitol and enalapril on renal inflammation and oxidative stress in ApoE-knock out mice.en_US
dc.description.abstractMETHODS: Animals treated for 4 mo as group (1) ApoE-knock out plus vehicle, group (2) ApoE-knock out plus paricalcitol (200 ng thrice a week), (3) ApoEknock out plus enalapril (30 mg/L), (4) ApoE-knock out plus paricalcitol plus enalapril and (5) normal. Blood pressure (BP) was recorded using tail cuff method. The kidneys were isolated for biochemical assays using spectrophotometer and Western blot analyses.
dc.description.abstractRESULTS: ApoE-deficient mice developed high BP (127 ± 3 mmHg) and it was ameliorated by enalapril and enalapril plus paricalcitol treatments but not with paricalcitol alone. Renal malondialdehyde concentrations, p22phox, manganese-superoxide dismutase, inducible nitric oxide synthase (NOS), monocyte chemoattractant protein-1, tumor necrosis factor-alpha and transforming growth factor-β1 levels significantly elevated but reduced glutathione, CuZn-SOD and eNOS levels significantly depleted in ApoE-knock out animals compared to normal. Administration of paricalcitol, enalapril and combined together ameliorated the renal inflammation and oxidative stress in ApoE-knock out animals.
dc.description.abstractRESULTS: ApoE-deficient mice developed high BP (127 ± 3 mmHg) and it was ameliorated by enalapril and enalapril plus paricalcitol treatments but not with paricalcitol alone. Renal malondialdehyde concentrations, p22phox, manganese-superoxide dismutase, inducible nitric oxide synthase (NOS), monocyte chemoattractant protein-1, tumor necrosis factor-alpha and transforming growth factor-β1 levels significantly elevated but reduced glutathione, CuZn-SOD and eNOS levels significantly depleted in ApoE-knock out animals compared to normal. Administration of paricalcitol, enalapril and combined together ameliorated the renal inflammation and oxidative stress in ApoE-knock out animals.
dc.description.abstractCONCLUSION: Paricalcitol and enalapril combo treatment ameliorates renal inflammation as well as oxidative stress in atherosclerotic animals.
dc.description.abstractCORE TIP: Although the protective efficacy of vitamin D and angiotensin converting enzyme inhibitors (ACEIs) have been studied in the cardiovascular system of atherosclerotic mice. However this is the first report to investigate the renal protection by paricalcitol and enalapril, alone or in combination in ApoE-deficient atherosclerotic mice. This innovative study clearly shows that vitamin D, ACEI and their combo ameliorated the renal inflammation and oxidative stress in ApoE-knock out animals by depleting the inflammatory and oxidative stress markers as well as restoring the renal antioxidant defense system in atherosclerotic mice. The combination of paricalcitol and enalapril warrants the clinical usefulness in renal atherosclerotic patients.
dc.language.isoenen_US
dc.publisherBaishideng Publishing Groupen_US
dc.relation.ispartofseriesv6, n3;
dc.subjectAtherosclerosisen_US
dc.subjectEnalapril
dc.subjectParicalcitol
dc.subjectRenal inflammation
dc.subjectOxidative stress
dc.titleEffect of paricalcitol and enalapril on renal inflammation/oxidative stress in atherosclerosisen_US
dc.typeArticleen_US
dc.description.DepartmentDepartment of Biologyen_US
dc.contributor.campusUniversity of Puerto Rico at Ponce


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