Long-term high-salt diet causes hypertension and decreases renal expression of vascular endothelial growth factor in Sprague-Dawley rats

被引:49
作者
Gu, Jian-Wei [1 ]
Bailey, Amelia P. [1 ]
Tan, Wei [1 ]
Shparago, Megan [1 ]
Young, Emily [1 ]
机构
[1] Univ Mississippi, Med Ctr, Dept Physiol & Biophys, Jackson, MS 39216 USA
关键词
Blood pressure; mean arterial pressure; renal injury; sFlt-1;
D O I
10.1016/j.jash.2008.03.001
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
We seek to determine: 1) whether a long-term high-salt (HS) diet induces hypertension and renal injury in Sprague-Dawley (SD) rats and 2) whether the HS diet-induced hypertension and renal injury are associated with decreased renal vascular endothelial growth factor (VEGF) expression. Twelve 10-week-old male SD rats received a HS diet (8%) and 12 SD rats received a normal salt diet (NS, 0.5%) for 8 weeks. Using a tail cuff, weekly monitoring showed that blood pressure (BP) increased significantly after 6, 7, and 8 weeks in the HS group, compared with the NS group (P < .01). At 4 weeks and 8 weeks of diet, mean arterial pressure (MAP) was determined in conscious rats by continuous monitoring through a catheter placed in the carotid artery. MAP was not significantly different between HS and NS group in 4 weeks, but was significantly higher in HS than NS group (140 +/- 5.3 vs. 112 +/- 2.2 mm Hg; P < .01) in 8 weeks. Increased proteinuria and albuminuria were associated with marked renal histologic abnormalities in the HS group, compared with those in the NS group. Northern blot and enzyme-linked immunosorbent assay (ELISA) demonstrated that 8 weeks of HS diet significantly decreased renal expression of VEGF mRNA and protein, compared with the NS group (P < .01). In 8 weeks, total urinary excretion of sFlt-1 was significantly higher in HS than NS group (9.28 +/- 1.05 vs. 2.05 +/- 0.55 ng/day; P < .01), whereas the plasma levels of sFlt-1 remained stable. These results suggest that a long-term HS diet induces renal injury and hypertension, which are associated with decreased renal VEGF expression in normotensive rodent animals. J Am Soc Hypertens 2008;2(4): 275-285. (C) 2008 American Society of Hypertension. All rights reserved.
引用
收藏
页码:275 / 285
页数:11
相关论文
共 51 条
[1]   Salt and hypertension - The debate that begs the bigger question [J].
Aviv, A .
ARCHIVES OF INTERNAL MEDICINE, 2001, 161 (04) :507-510
[2]   Time course of synergistic interaction between DOCA and salt on blood pressure: roles of vasopressin and hepatic osmoreceptors [J].
Brooks, Virginia L. ;
Freeman, Korrina L. ;
Qi, Yue .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2006, 291 (06) :R1825-R1834
[3]   HIGH SALT INTAKE AND BLOOD-PRESSURE IN LOWER PRIMATES (PAPIO-HAMADRYAS) [J].
CHERCHOVICH, GM ;
CAPEK, K ;
JEFREMOVA, Z ;
POHLOVA, I ;
JELINEK, J .
JOURNAL OF APPLIED PHYSIOLOGY, 1976, 40 (04) :601-604
[4]   UTILIZATION OF SWINE TO STUDY THE RISK FACTOR OF AN ELEVATED SALT DIET ON BLOOD-PRESSURE [J].
CORBETT, WT ;
KULLER, LH ;
BLAINE, EH ;
DAMICO, FJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1979, 32 (10) :2068-2075
[5]   EFFECTS OF CHRONIC EXCESS SALT INGESTION - ROLE OF GENETIC FACTORS IN BOTH DOCA-SALT AND RENAL HYPERTENSION [J].
DAHL, LK ;
HEINE, M ;
TASSINARI, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 1963, 118 (04) :605-&
[6]   THE EFFECT OF INCREASED SALT INTAKE ON BLOOD-PRESSURE OF CHIMPANZEES [J].
DENTON, D ;
WEISINGER, R ;
MUNDY, NI ;
WICKINGS, EJ ;
DIXSON, A ;
MOISSON, P ;
PINGARD, AM ;
SHADE, R ;
CAREY, D ;
ARDAILLOU, R ;
PAILLARD, F ;
CHAPMAN, J ;
THILLET, J ;
MICHEL, JB .
NATURE MEDICINE, 1995, 1 (10) :1009-1016
[7]  
DIBONA GF, 1986, P SOC EXP BIOL MED, V182, P43
[8]   RENAL NERVES ARE NOT NECESSARY FOR ONSET OR MAINTENANCE OF DOC-SALT HYPERTENSION IN RATS [J].
DZIELAK, DJ ;
NORMAN, RA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (05) :H945-H949
[9]  
ELLIOTT P, 1988, BRIT MED J, V297, P319
[10]   Glomerular-specific alterations of VEGF-A expression lead to distinct congenital and acquired renal diseases [J].
Eremina, V ;
Sood, M ;
Haigh, J ;
Nagy, A ;
Lajoie, G ;
Ferrara, N ;
Gerber, HP ;
Kikkawa, Y ;
Miner, JH ;
Quaggin, SE .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (05) :707-716