REDUCED OXYGENATION IN DIABETIC RAT KIDNEYS MEASURED BY T2*WEIGHTED MAGNETIC RESONANCE MICRO-IMAGING

被引:25
作者
Edlund, Jenny [1 ]
Hansell, Peter [1 ]
Fasching, Angelica [1 ]
Liss, Per [2 ]
Weis, Jan [2 ]
Glickson, Jerry D. [3 ]
Palm, Fredrik [1 ,4 ]
机构
[1] Uppsala Univ, Dept Med Cell Biol, BMC, S-75123 Uppsala, Sweden
[2] Univ Uppsala Hosp, Dept Oncol Radiol & Clin Immunol, S-75123 Uppsala, Sweden
[3] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
[4] Georgetown Univ, Dept Med, Washington, DC USA
来源
OXYGEN TRANSPORT TO TISSUE XXX | 2009年 / 645卷
关键词
MRI;
D O I
10.1007/978-0-387-85998-9_31
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
By applying invasive techniques for direct measurements of oxygen tension, we have reported decreased kidney oxygenation in experimental diabetes in rats. However, the non-invasive MRI technique utilizing the BOLD effect provides several advantages with the possibility to perform repetitive measurements in the same animals and in human Subjects. In this study, we applied a modified single gradient echo microimaging sequence to detect the BOLD effect in kidneys of diabetic rats and compared the results to normoglycemic controls. All measurements were performed oil inactin-anaesthetized adult male Wistar Furth rats. Diabetes was induced by streptozotocin (45 mg/kg) 14 days prior to MRI-analysis. Sixteen T2*-weighted image records (B(0)=1.5 T) were performed using radiofrequency spoiled gradient echo sequence with 2.6 mls step increments of TE (TE(1)=12 ills), while TR (75 ms) and bandwidth per pixel (71.4 Hz) were kept constant. T2* maps were Computed by mono-exponential fitting of the pixel intensities. Relaxation rates R2* (1/T2*) in cortex and outer stripe of the outer medulla were similar in both groups (cortex for controls 22.3 +/- 0.4 vs. diabetics 23.1 +/- 1.8 Hz and outer stripe of outer medulla for controls 24.9 +/- 0.4 vs. diabetics 26.4 +/- 1.8 Hz; n=4 in both groups), whereas R2* was increased in the inner stripe Of the Outer medulla in diabetic rats (diabetics 26.1 +/- 2.4 vs. controls 18.8 +/- 1.4 Hz; n=4, P<0.05). This Study demonstrates that experimental diabetes in rats induces decreased oxygenation of the renal Outer medulla. Furthermore, the proposed T2*-weighted MR micro-imaging technique is Suitable for detection of regional changes in kidney oxygenation in experimental animal models.
引用
收藏
页码:199 / 204
页数:6
相关论文
共 11 条
[1]   Early changes with diabetes in renal medullary hemodynamics as evaluated by fiberoptic probes and BOLD magnetic resonance imaging [J].
dos Santos, Elisabete Aleantara ;
Li, Lu-Ping ;
Ji, Lin ;
Prasad, Pottumarthi Vara .
INVESTIGATIVE RADIOLOGY, 2007, 42 (03) :157-162
[2]   Issues in flow and oxygenation dependent contrast (FLOOD) imaging of tumours [J].
Howe, FA ;
Robinson, SP ;
McIntyre, DJO ;
Stubbs, M ;
Griffiths, JR .
NMR IN BIOMEDICINE, 2001, 14 (7-8) :497-506
[3]   Kidneys in hypertensive rats show reduced response to nitric oxide synthase inhibition evaluated by BOLD MRI [J].
Li, LP ;
Storey, P ;
Kim, D ;
Li, W ;
Prasad, P .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2003, 17 (06) :671-675
[4]   Reduced nitric oxide concentration in the renal cortex of streptozotocin-induced diabetic rats - Effects on renal oxygenation and microcirculation [J].
Palm, F ;
Buerk, DG ;
Carlsson, PO ;
Hansell, P ;
Liss, P .
DIABETES, 2005, 54 (11) :3282-3287
[5]   Polyol-pathway-dependent disturbances in renal medullary metabolism in experimental insulin-deficient diabetes mellitus in rats [J].
Palm, F ;
Hansell, P ;
Ronquist, G ;
Waldenström, A ;
Liss, P ;
Carlsson, PO .
DIABETOLOGIA, 2004, 47 (07) :1223-1231
[6]   Reactive oxygen species cause diabetes-induced decrease in renal oxygen tension [J].
Palm, F ;
Cederberg, J ;
Hansell, P ;
Liss, P ;
Carlsson, PO .
DIABETOLOGIA, 2003, 46 (08) :1153-1160
[7]   Intrarenal oxygen in diabetes and a possible link to diabetic nephropathy [J].
Palm, Fredrik .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2006, 33 (10) :997-1001
[8]   Functional MRI of the kidney: tools for translational studies of pathophysiology of renal disease [J].
Prasad, PV .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2006, 290 (05) :F958-F974
[9]  
WEIS J, 1989, Z NATURFORSCH A, V44, P1151
[10]  
Weis J, 1999, MAGNET RESON MED, V41, P904, DOI 10.1002/(SICI)1522-2594(199905)41:5<904::AID-MRM8>3.0.CO