Kidney International (1997) 51, 50–56; doi:10.1038/ki.1997.7
Relationship between MRI and morphometric kidney measurements in diabetic and non-diabetic rats
Thora Christiansen1, R Rasch1, H Stødkilde-Jørgensen1 and A Flyvbjerg1
1Experimental MRI-Center, University Hospital, and Department of Cell Biology, Institute of Anatomy, and Institute of Experimental Clinical Research, University Hospital, University of Aarhus, Aarhus, Denmark
Correspondence: Dr Thora Christiansen, Experimental MRI-Center, University Hospital, Skejby Sygehus, DK-8200 Aarhus N, Denmark.
Received 22 May 1996; Revised 26 August 1996; Accepted 26 August 1996.
Top of pageAbstract
Relationship between MRI and morphometric kidney measurements in diabetic and non-diabetic rats. The aim of the present study was to determine the applicability of magnetic resonance imaging (MRI) as a non-invasive measure of kidney volume in vivo in diabetic and non-diabetic rats. Magnetic resonance, T1 weighted Spin Echo, images were obtained after injection of contrast in anesthetized control (N = 14) and hyperglycemic streptozotocin (STZ)-diabetic rats (N = 14). On MRI imaging the total kidney, cortex, medullary and pelvic volumes were calculated. Immediately after MRI measurements the left kidneys were removed before weighing either as a clamped kidney weight (that is, the kidney containing blood and urine) or as a wet kidney weight (the kidney drained of blood and urine), while the right kidneys were perfusion-fixed for morphometric measurements. On thin kidney slices obtained from perfusion-fixed kidneys the cortex, medullary and pelvic fractions were measured and subsequently the cortex, medulla and pelvic volumes were calculated. The cortical volume was measured according to three different approaches. The corticomedullary boundary was defined either to the arcuate arteries, to a curved line following the glomeruli, or to a line at the top of the medullary rays. Both in control and diabetic rats, MRI measured kidney volumes were similar to the volume of perfusion-fixed kidneys, while the clamped kidney weight, and in particular the wet kidney weights, were smaller than the MRI obtained volumes. Good agreement was found between the MRI measured cortex and medulla volumes when the cortex was defined to the top of the medullary rays in the morphometric analysis. In conclusion, the present study demonstrates that MRI allows a reliable non-invasive estimate of renal morphology at a macroscopic level in both diabetic and non-diabetic rats.
Top of pageReferences
- Mogensen CE, Christensen CK: Predicting diabetic nephropathy in insulin-dependent patients. N Engl J Med 311:89–93, 1984 | PubMed | ISI | ChemPort |
- Seyer-Hansen K: Renal hypertrophy in experimental diabetes. Kidney Int 23:643–646, 1983 | PubMed | ChemPort |
- Ørskov H, Olsen TS, Nielsen K, Rafaelsen OJ, Lundbæk K: Kidney lesions in rats with servere long-term alloxan diabetes. Influence of age, alloxan damage, and insulin administration. Diabetologia 1:172–179, 1965
- Seyer-Hansen K: Renal hypertrophy in streptozotocin diabetes rat. Clin Sci Mol Med 51:551–555, 1976 | ChemPort |
- Seyer-Hansen K, Hansen J, Gundersen HJG: Renal hypertrophy in experimental diabetes: A morphometric study. Diabetologia 18:501–515, 1980 | PubMed | ChemPort |
- Østerby R, Gundersen HJG: Glomerular size and structure in diabetes mellitus. I. Early abnormalities. Diabetologia 11:225–229, 1975 | PubMed | ISI | ChemPort |
- Rasch R: Prevention of diabetic glomerulopathy in streptozotocin diabetes rats by insulin treatment: Kidney size and glomerular volume. Diabetologia 16:125–128, 1979
- Rasch R: Prevention of diabetic glomerulopathy in streptozotocin diabetic rats by insulin treatment: Albumin excretion. Diabetologia 18:413–416, 1980
- Flyvbjerg A, Thorlacius-Ussing O, Næraa R, Ingerslev J, Ørskov H: Kidney tissue somatomedin C and initial renal growth in diabetic and uninephrectomized rats. Diabetologia 31:310–314, 1988 | PubMed | ISI | ChemPort |
- Nyengaard JR, Flyvbjerg A, Rasch R: The impact of renal growth, regression and regrowth in experimental diabetes mellitus on number and size of proximal and distal tubular cells in rat kidney. Diabetologia 36:1126–1131, 1993 | PubMed | ISI | ChemPort |
- Stackhouse S, Miller PL, Park SK, Meyer TW: Reversal of glomerular hyperfiltration and renal hypertrophy by blood glucose normalization in diabetes rats. Diabetes 39:989–995, 1990
- Grønbæk H, Nielsen B, Østerby R, Harris AG, Ørskov H, Flyvbjerg A: Effect of octreotide on manifest renal and glomerular hypertrophy and urinary albumin excretion in long-term experimental diabetes in rats. Diabetologia 38:135–144, 1995
- Hricak H, Crooks L, Sheldon P, Kaufman L: Nuclear magnetic resonance imaging of the kidney. Radiology 146:425–432, 1983
- Hricak H, Newhouse J: MR imaging of the kidney. Radiol Clin N Am 22:287–296, 1984
- Lipuma J: Magnetic resonance imaging of the kidney. Radiol Clin N Am 22:925–941, 1984
- London D, Davis P, Williams R, Crooks L, Sheldon P, Gooding C: Nuclear magnetic resonance imaging of induced renal lesions. Radiology 148:167–172, 1983
- Mitchell DG, Tobin M, Le Veen R, Tomaczewski J, Lavi A, Staum M, Kundel LH: Induced renal artery stenosis in rabbits: Magnetic resonance imaging, angiography, and radionuclide determination of blood volume and bloodflow. Magn Resn Imaging 6:113–124, 1988
- Thickman D, Kundel H, Biery D: Magnetic resonance evaluation of hydronephrosis in dog. Radiology 152:113–116, 1984
- Iana A, Weininger J, Abrashkin S: Paramagnetic enhanced proton magnetic resonance measurements in rats correlates with renal function. Magn Reson Imaging 6:131–134, 1988
- Abrashkin S, Weininger J, Griffel L, Schneider R, Iana A: Proton magnetic resonance in experimental acute and chronic renal failure in rats. Renal Failure 10:21–27, 1987
- Carvling MJ, Arger PH, Kundel HL, Axel L, Dougherty L, Kassab EA, Moore B: Acute tubular necrosis: Use of gadolinium DTPA and fast MR imaging to evaluate renal function in the rabbit. JCAT 11:488–495, 1987
- Iana A, Abrashkin S, Weininger J: Proton MR study of different types of experimental acute renal failure in rats. Magn Reson Imaging 4:241–244, 1986
- Yuasa Y, Kundel H: Magnetic resonance imaging following unilateral occlusion of the renal circulation in rabbits. Radiology 154:151–156, 1985
- Maunsbach AB: The influence of different fixatives and fixation methods on the ulterstructure of rat kidney proximal tubule cells I. Comparison of different perfusion fixation methods and of glutaraldehyde and osmium tetraoxide fixatives. J Ultrastr Res 15:232–282, 1966
- Baddeley AJ, Gundersen HJG, Cruz-Orive LM: Estimation of surface area from vertical sections. J Microsc 142:259–276, 1986 | PubMed | ISI | ChemPort |
- Gundersen HJG, Jensen EB: The efficiency of systematic sampling in stereology and its prediction. J Microsc 147:229–263, 1987 | PubMed | ISI | ChemPort |
- Kriz W, Bankir L: A standard nomenclature for structures of the kidney. Kidney Int 33:1–7, 1988 | PubMed | ChemPort |
- Bland JM, Altman DG: Statistical methods for assessing agreement between two methods of clinical measurements. Lancet i:307–310, 1986
- Lohr J, Mazurchuk RJ, Acara MA, Nickerson PA, Fiel RJ: MRI and patophysiology of the rat kidney. Magn Reson Imaging 9:93–100, 1991
- Hricak H, Newhouse JH: MR imaging of the kidney. Radiol Clin N Am 22:287–296, 1984
- Basgen JM, Steffes MW, Stillman AE, Mauer SM: Estimating glomerular number in situ using magnetic resonance imaging and biopsy. Kidney Int 45:1668–1672, 1994 | PubMed | ISI | ChemPort |
- Meyer RA, Cooper TG, Potchen EJ: Measurement of blood flow in rat poplitea vessel by Phase contrast MR angiography. (abstract) Proc Soc Magn Res 992, 1994