A rat model of chronic kidney disease-mineral bone disorder

被引:127
作者
Moe, Sharon M. [1 ,2 ]
Chen, Neal X. [1 ]
Seifert, Mark F. [3 ]
Sinders, Rachel M. [3 ]
Duan, Dana [1 ]
Chen, Xianming [1 ]
Liang, Yun [4 ]
Radcliff, J. Scott [5 ]
White, Kenneth E. [6 ]
Gattone, Vincent H., II [3 ]
机构
[1] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46260 USA
[2] Richard L Roudebush Vet Affairs Med Ctr, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Anat, Indianapolis, IN 46260 USA
[4] Indiana Univ, Sch Med, Dept Radiol, Indianapolis, IN 46260 USA
[5] Purdue Univ, Dept Anim Sci, Lafayette, IN USA
[6] Indiana Univ, Sch Med, Dept Genet, Indianapolis, IN 46260 USA
关键词
vascular calcification; renal osteodystrophy; chronic kidney disease; hyperphosphatemia; hyperparathyroidism; CORONARY-ARTERY CALCIFICATION; SUBTOTALLY NEPHRECTOMIZED RATS; CHRONIC-RENAL-FAILURE; VASCULAR CALCIFICATION; SECONDARY HYPERPARATHYROIDISM; SEVELAMER HYDROCHLORIDE; CALCIUM-CARBONATE; PROTEIN-DIET; UREMIC RATS; PROGRESSION;
D O I
10.1038/ki.2008.456
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Chronic Kidney Disease-Mineral Bone Disorder (CKD-MBD) is a newly defined syndrome encompassing patients with chronic kidney disease that have a triad of biochemical alterations in calcium, phosphorus and parathyroid hormone, vascular calcification, and bone abnormalities. Here we describe a novel Cy/+ rat model of slowly progressive kidney disease spontaneously developing the three components of CKD-MBD when fed a normal phosphorus diet. Since the renal disorder progressed 'naturally' we studied the effect of dietary manipulation during the course of the disease. Animals with early, but established, chronic kidney disease were fed a casein-based or a grain-based protein diet both of which had equivalent total phosphorus contents. The two different sources of dietary protein had profound effects on the progression of CKD-MBD, likely due to differences in intestinal bioavailability of phosphorus. Although both dietary treatments resulted in the same serum phosphorous levels, the casein-fed animals had increased urinary phosphorus excretion and elevated serum FGF23 compared to the grain-fed rats. This model should help identify early changes in the course of chronic kidney disease that may lead to CKD-MBD.
引用
收藏
页码:176 / 184
页数:9
相关论文
共 35 条
[1]
Dietary soy protein effects on disease and IGF-I in male and female Han:SPRD-cy rats [J].
Aukema, HM ;
Housini, I .
KIDNEY INTERNATIONAL, 2001, 59 (01) :52-61
[2]
Phytase, high-available-phosphorus corn, and storage effects on phosphorus levels in pig excreta [J].
Baxter, CA ;
Joern, BC ;
Ragland, D ;
Sands, JS ;
Adeola, O .
JOURNAL OF ENVIRONMENTAL QUALITY, 2003, 32 (04) :1481-1489
[3]
Effects of sevelamer and calcium on coronary artery calcification in patients new to hemodialysis [J].
Block, GA ;
Spiegel, DM ;
Ehrlich, J ;
Mehta, R ;
Lindbergh, J ;
Dreisbach, A ;
Raggi, P .
KIDNEY INTERNATIONAL, 2005, 68 (04) :1815-1824
[4]
Missense mutation in sterile α motif of novel protein SamCystin is associated with polycystic kidney disease in (cy/+) rat [J].
Brown, JH ;
Bihoreau, MT ;
Hoffmann, S ;
Kränzlin, B ;
Tychinskaya, I ;
Obermüller, N ;
Podlich, D ;
Boehn, SN ;
Kaisaki, PJ ;
Megel, N ;
Danoy, P ;
Copley, RR ;
Broxholme, J ;
Witzgall, R ;
Lathrop, M ;
Gretz, N ;
Gauguier, D .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (12) :3517-3526
[5]
Fetuin-A uptake in bovine vascular smooth muscle cells is calcium dependent and mediated by annexins [J].
Chen, Neal X. ;
O'Neill, Kalisha D. ;
Chen, Xianming ;
Duan, Danxia ;
Wang, Exing ;
Sturek, Michael S. ;
Edwards, Jason M. ;
Moe, Sharon M. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2007, 292 (02) :F599-F606
[6]
Gender and the effect of gonadal hormones on the progression of inherited polycystic kidney disease in rats [J].
Cowley, BD ;
Rupp, JC ;
Muessel, MJ ;
Gattone, VH .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1997, 29 (02) :265-272
[7]
AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE IN THE RAT [J].
COWLEY, BD ;
GUDAPATY, S ;
KRAYBILL, AL ;
BARASH, BD ;
HARDING, MA ;
CALVET, JP ;
GATTONE, VH .
KIDNEY INTERNATIONAL, 1993, 43 (03) :522-534
[8]
Modification of disease progression in rats with inherited polycystic kidney disease [J].
Cowley, BD ;
Grantham, JJ ;
Muessel, MJ ;
Kraybill, AL ;
Gattone, VH .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 27 (06) :865-879
[9]
The effects of sevelamer hydrochloride and calcium carbonate on kidney calcification in uremic rats [J].
Cozzolino, M ;
Dusso, AS ;
Liapis, H ;
Finch, J ;
Lu, Y ;
Burke, SK ;
Slatopolsky, E .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2002, 13 (09) :2299-2308
[10]
BMP-7 is an efficacious treatment of vascular calcification in a murine model of atherosclerosis and chronic renal failure [J].
Davies, MR ;
Lund, RJ ;
Hruska, KA .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (06) :1559-1567