Role of hyperhomocysteinemia in the regulation of oxidative stress and inflammatory responses in the kidney: protective effect of folic acid supplementation

dc.contributor.authorHwang, Sun-Young
dc.contributor.examiningcommitteeGuenter, Bill (Animal Science) House, Jamnes (Animal Science) Suh, Miyoung (Human Nutritional Science)en_US
dc.contributor.supervisorO, Karmin (Animal Science)en_US
dc.date.accessioned2012-01-10T21:56:46Z
dc.date.available2012-01-10T21:56:46Z
dc.date.issued2011
dc.degree.disciplineAnimal Scienceen_US
dc.degree.levelDoctor of Philosophy (Ph.D.)en_US
dc.description.abstractHyperhomocysteinemia, a condition of elevated blood homocysteine (Hcy) level, is an independent risk factor for cardiovascular disease. Folic acid supplementation can effectively reduce blood Hcy levels. Recent studies have demonstrated that hyperhomocysteinemia is also associated with kidney disease. However, the underlying mechanisms remain unclear. The overall objective of the study was to investigate the biochemical and molecular mechanisms of Hcy-induced kidney injury and the effect of folic acid supplementation on Hcy-induced kidney injury. Hyperhomocysteinemia was induced in Sprague-Dawley rats by feeding a high-methionine diet for 12 weeks. An elevation of serum total Hcy level was observed in hyperhomocysteinemic rats. Hyperhomocysteinemia-induced superoxide anion production via nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activation resulted in oxidative stress in the kidney. Reduction of oxidative stress by inhibiting superoxide anion production effectively ameliorated hyperhomocysteinemia-induced kidney injury. Inflammatory responses such as increased chemokine expression have been implicated as one of the mechanisms of kidney disease. Monocyte chemoattractant protein-1 (MCP-1) is a potent chemokine that is involved in the inflammatory response in kidney disease. Nuclear factor-kappa B (NF-kappaB) plays an important role in upregulation of MCP-1 expression. We investigated the effect of hyperhomocysteinemia on MCP-1 expression and the molecular mechanism responsible for such an effect in rat kidneys as well as in human kidney proximal tubular cells.en_US
dc.description.noteFebruary 2012en_US
dc.identifier.urihttp://hdl.handle.net/1993/5066
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectHomocysteineen_US
dc.subjectKidney Diseaseen_US
dc.titleRole of hyperhomocysteinemia in the regulation of oxidative stress and inflammatory responses in the kidney: protective effect of folic acid supplementationen_US
dc.typedoctoral thesisen_US
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