Increased renal iron accumulation in hypertensive nephropathy of salt-loaded hypertensive rats

• Published in: PloS one 2013-10, Vol.8 (10), p.e75906-e75906
• Main Authors: Naito, Yoshiro, Sawada, Hisashi, Oboshi, Makiko, Fujii, Aya, Hirotani, Shinichi, Iwasaku, Toshihiro, Okuhara, Yoshitaka, Eguchi, Akiyo, Morisawa, Daisuke, Ohyanagi, Mitsumasa, Tsujino, Takeshi, Masuyama, Tohru
• Format: Article
• Language: English
• Subjects: Accumulation; Animals; Blood Pressure - drug effects; Cardiovascular disease; Cation Transport Proteins - metabolism; Cellulose; Chronic kidney failure; Deoxyguanosine; Diet; Divalent metal transporter-1; Excretion; Experiments; Gene expression; Hypertension; Hypertension, Renal - etiology; Hypertension, Renal - metabolism; Hypertension, Renal - pathology; Internal medicine; Iron; Iron - metabolism; Iron content; Iron transport; Kidney - metabolism; Kidney - pathology; Kidney diseases; Kidneys; Laboratory animals; Male; Medicine; Metabolism; Nephritis - etiology; Nephritis - metabolism; Nephritis - pathology; Nephropathy; Nephrosclerosis - etiology; Nephrosclerosis - metabolism; Nephrosclerosis - pathology; Nutrient deficiency; Oxidative stress; Pathogenesis; Potassium; Proteins; Rats; Rats, Inbred SHR; Receptors, Transferrin - metabolism; Rodents; Salts; Sodium Chloride, Dietary - administration & dosage; Stroke; Superoxide; Survival; Transferrin; Transporter; Tubules; Urine
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0075906

Although iron is reported to be associated with the pathogenesis of chronic kidney disease, it is unknown whether iron participates in the pathophysiology of nephrosclerosis. Here, we investigate whether iron is involved in the development of hypertensive nephropathy and the effects of iron restriction on nephrosclerosis in salt- loaded stroke-prone spontaneously hypertensive rats (SHRSP). SHRSP were given either a normal or high-salt diet for 8 weeks. Another subset of SHRSP were fed a high-salt with iron-restricted diet. SHRSP given a high-salt diet developed severe hypertension and nephrosclerosis. As a result, survival rate was decreased after 8 weeks diet. Importantly, massive iron accumulation and increased iron content were observed in the kidneys of salt-loaded SHRSP, along with increased superoxide production, urinary 8-Hydroxy-2'-deoxyguanosine excretion, and urinary iron excretion; however, these changes were markedly attenuated by iron restriction. Of interest, expression of cellular iron transport proteins, transferrin receptor 1 and divalent metal transporter 1, was increased in the tubules of salt-loaded SHRSP. Notably, iron restriction attenuated the development of severe hypertension and nephrosclerosis, thereby improving survival rate in salt-loaded SHRSP. Taken together, these results suggest a novel mechanism by which iron plays a role in the development of hypertensive nephropathy and establish the effects of iron restriction on salt-induced nephrosclerosis.