Molecular targets of hyperphosphataemia in chronic renal failure

被引:20
作者
Miyamoto, KI [1 ]
Ito, M [1 ]
Segawa, H [1 ]
Kuwahata, M [1 ]
机构
[1] Univ Tokushima, Dept Nutr, Sch Med, Tokushima 7708503, Japan
关键词
chronic renal failure; dietary phosphate; hyperphosphataemia; klotho; secondary hyperparathyroidism;
D O I
10.1093/ndt/gfg1020
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Dietary phosphate restriction can prevent or retard the progress of chronic renal failure (CRF) and secondary hyperparathyroidism. The klotho gene is involved in the development of a syndrome resembling human ageing, and klotho mutant mice show abnormal calcium/vitamin D metabolism, developing hyperphosphataemia and vascular calcification. Phosphate retention rescues the phenotype of klotho mice. The level of expression of klotho RNA was greatly reduced in the kidneys of all CRF patients. Dietary P-i restriction induced klotho expression, which enhances the beneficial effect of P-i restriction in patients with CRF and/or on haemodialysis.
引用
收藏
页码:79 / 80
页数:2
相关论文
共 9 条
[1]   Disorders of phosphate metabolism in chronic renal disease [J].
Edwards, RM .
CURRENT OPINION IN PHARMACOLOGY, 2002, 2 (02) :171-176
[2]   Identification of regulatory sequences and binding proteins in the type II sodium/phosphate cotransporter NPT2 gene responsive to dietary phosphate [J].
Kido, S ;
Miyamoto, K ;
Mizobuchi, H ;
Taketani, Y ;
Ohkido, I ;
Ogawa, N ;
Kaneko, Y ;
Harashima, S ;
Takeda, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (40) :28256-28263
[3]   Severely reduced production of Klotho in human chronic renal failure kidney [J].
Koh, N ;
Fujimori, T ;
Nishiguchi, S ;
Tamori, A ;
Shiomi, S ;
Nakatani, T ;
Sugimura, K ;
Kishimoto, T ;
Kinoshita, S ;
Kuroki, T ;
Nabeshima, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (04) :1015-1020
[4]   Mutation of the mouse klotho gene leads to a syndrome resembling ageing [J].
Kuroo, M ;
Matsumura, Y ;
Aizawa, H ;
Kawaguchi, H ;
Suga, T ;
Utsugi, T ;
Ohyama, Y ;
Kurabayashi, M ;
Kaname, T ;
Kume, E ;
Iwasaki, H ;
Iida, A ;
ShirakiIida, T ;
Nishikawa, S ;
Nagai, R ;
Nabeshima, Y .
NATURE, 1997, 390 (6655) :45-51
[5]   Proximal tubular phosphate reabsorption: Molecular mechanisms [J].
Murer, H ;
Hernando, N ;
Forster, I ;
Biber, J .
PHYSIOLOGICAL REVIEWS, 2000, 80 (04) :1373-1409
[6]   Structure of the mouse klotho gene and its two transcripts encoding membrane and secreted protein [J].
Shiraki-Iida, T ;
Aizawa, H ;
Matsumura, Y ;
Sekine, S ;
Iida, A ;
Anazawa, H ;
Nagai, R ;
Kuro-o, M ;
Nabeshima, Y .
FEBS LETTERS, 1998, 424 (1-2) :6-10
[7]   Mechanisms of secondary hyperparathyroidism [J].
Silver, J ;
Kilav, R ;
Naveh-Many, T .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2002, 283 (03) :F367-F376
[8]   Role of phosphorus in the pathogenesis of secondary hyperparathyroidism [J].
Slatopolsky, E ;
Brown, A ;
Dusso, A .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 37 (01) :S54-S57
[9]   Mediation of unusually high concentrations of 1,25-dihydroxyvitamin D in homozygous klotho mutant mice by increased expression of renal 1α-hydroxylase gene [J].
Yoshida, T ;
Fujimori, T ;
Nabeshima, Y .
ENDOCRINOLOGY, 2002, 143 (02) :683-689