Iron restriction inhibits renal injury in aldosterone/salt-induced hypertensive mice

被引:17
作者
Sawada, Hisashi [1 ]
Naito, Yoshiro [1 ]
Oboshi, Makiko [1 ]
Iwasaku, Toshihiro [1 ]
Okuhara, Yoshitaka [1 ]
Morisawa, Daisuke [1 ]
Eguchi, Akiyo [1 ]
Hirotani, Shinichi [1 ]
Masuyama, Tohru [1 ]
机构
[1] Hyogo Coll Med, Dept Internal Med, Div Cardiovasc, Nishinomiya, Hyogo 6638501, Japan
关键词
aldosterone; iron; renal injury; salt; transferrin receptor 1; CHRONIC KIDNEY-DISEASE; OXIDATIVE STRESS; DEFICIENCY PROTECTS; RAT MODEL; FIBROSIS; DAMAGE; INFLAMMATION; EXPRESSION;
D O I
10.1038/hr.2015.13
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Excess iron is associated with the pathogenesis of several renal diseases. Aldosterone is reported to have deleterious effects on the kidney, but there have been no reports of the role of iron in aldosterone/salt-induced renal injury. Therefore, we investigated the effects of dietary iron restriction on the development of hypertension and renal injury in aldosterone/salt-induced hypertensive mice. Ten-week-old male C57BL/6J mice were uninephrectomized and infused with aldosterone for four weeks. These were divided into two groups: one fed a high-salt diet (Aldo) and the other fed a high-salt with iron-restricted diet (Aldo-IR). Vehicle-infused mice without a uninephrectomy were also divided into two groups: one fed a normal diet (control) and the other fed an iron-restricted diet (IR) for 4 weeks. As compared with control and IR mice, Aldo mice showed an increase in both systolic blood pressure and urinary albumin/creatinine ratio, but these increases were reduced in the Aldo-IR group. In addition, renal histology revealed that Aldo mice exhibited glomerulosclerosis and tubulointerstitial fibrosis, whereas these changes were attenuated in Aldo-IR mice. Expression of intracellular iron transport protein transferrin receptor 1 was increased in the renal tubules of Aldo mice compared with control mice. Dietary iron restriction attenuated the development of hypertension and renal injury in aldosterone/salt-induced hypertensive mice.
引用
收藏
页码:317 / 322
页数:6
相关论文
共 25 条
[1]   Aldosterone/salt induces renal inflammation and fibrosis in hypertensive rats [J].
Blasi, ER ;
Rocha, R ;
Rudolph, AE ;
Blomme, EAG ;
Polly, ML ;
McMahon, EG .
KIDNEY INTERNATIONAL, 2003, 63 (05) :1791-1800
[2]   Plasma aldosterone is independently associated with the metabolic syndrome [J].
Bochud, Murielle ;
Nussberger, Jurg ;
Bovet, Pascal ;
Maillard, Marc R. ;
Elston, Robert C. ;
Paccaud, Fred ;
Shamlaye, Conrad ;
Burnier, Michel .
HYPERTENSION, 2006, 48 (02) :239-245
[3]   Spironolactone in addition to ACE inhibition to reduce proteinuria in patients with chronic renal disease. [J].
Chrysostomou, A ;
Becker, G .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (12) :925-926
[4]   The transferrin receptor part I: Biology and targeting with cytotoxic antibodies for the treatment of cancer [J].
Daniels, Tracy R. ;
Delgado, Tracie ;
Rodriguez, Jose A. ;
Helguera, Gustavo ;
Penichet, Manuel L. .
CLINICAL IMMUNOLOGY, 2006, 121 (02) :144-158
[5]   Mizoribine Ameliorates Renal Injury and Hypertension along with the Attenuation of Renal Caspase-1 Expression in Aldosterone-Salt-Treated Rats [J].
Doi, Toshiki ;
Doi, Shigehiro ;
Nakashima, Ayumu ;
Ueno, Toshinori ;
Yokoyama, Yukio ;
Kohno, Nobuoki ;
Masaki, Takao .
PLOS ONE, 2014, 9 (04)
[6]  
Halimi JM, 1995, J HYPERTENS, V13, P1801
[7]   Osteopontin deficiency protects against aldosterone-induced inflammation, oxidative stress, and interstitial fibrosis in the kidney [J].
Irita, Jun ;
Okura, Takafumi ;
Jotoku, Masanori ;
Nagao, Tomoaki ;
Enomoto, Daijiro ;
Kurata, Mie ;
Desilva, Veena Rasika ;
Miyoshi, Ken-ichi ;
Matsui, Yutaka ;
Uede, Toshimitsu ;
Denhardt, David T. ;
Rittiling, Susan R. ;
Higaki, Jitsuo .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2011, 301 (04) :F833-F844
[8]   Labile iron pool: the main determinant of cellular response to oxidative stress [J].
Kruszewski, M .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 531 (1-2) :81-92
[9]   Iron-deficient diet reduces atherosclerotic lesions in ApoE-deficient mice [J].
Lee, TS ;
Shiao, MS ;
Pan, CC ;
Chau, LY .
CIRCULATION, 1999, 99 (09) :1222-1229
[10]   Plasminogen activator inhibitor-1 deficiency protects against aldosterone-induced glomerular injury [J].
Ma, J ;
Weisberg, A ;
Griffin, JP ;
Vaughan, DE ;
Fogo, AB ;
Brown, NJ .
KIDNEY INTERNATIONAL, 2006, 69 (06) :1064-1072