Determinants of glomerular filtration and plasma flow in experimental diabetic rats.

GFR and, to a lesser extent, RPF are elevated soon after the onset of human diabetes mellitus. The mechanisms involved in these functional changes are unknown. Since the experimental diabetic rat has renal morphological changes similar to those observed in man, we investigated whole-kidney and superficial-nephron glomerular function in this animal model early during the course of the disease. Alloxan-induced diabetes (50 mg/kg BW) is frequently characterized by severe hyperglycemia and retarded body growth. Supplemental insulin administration (6 U of NPH insulin daily) results in normal body growth, although hyperglycemia persists. As a result, we studied four groups of diabetic rats (1) after 1 month of untreated diabetes, (2) after 3 months of untreated diabetes, (3) after 3 months of untreated diabetes followed by 1 month of insulin supplementation, and (4) after 3 months of insulin-supplemented diabetes. After 1 month of untreated diabetes, GFR and SNGFR each declined by 20% compared to age-matched control rats. RPF and SNGFR were both reduced by 33% as a consequence of a 41% increase in RT. Reduced SNGPF together with a 7 mm Hg reduction in PGC caused the fall in GFR and SNGFR. KWs were not significantly different from those of control rats. The functional changes that occurred after 1 month of untreated diabetes did not significantly deteriorate after 3 months of the disease. Insulin supplementation, when instituted for 1 month after 3 months of untreated diabetes, produced no significant improvement in either whole-kidney or superficial-nephron hemodynamics even though body and kidney growth were stimulated. In contrast, insulin supplementation initiated at the onset of diabetes increased both SNGFR and SNGFR to 23% above control values. GFR and RPF each increased in proportion to the 18% increment in kidney size. RT was reduced in these rats, and the pressures that govern glomerular ultrafiltration were not altered from control values. We conclude that in untreated diabetic rats, an increase in RT is the predominant hemodynamic alteration which produces reduced glomerular hemodynamic function. Once established, this defect may not be reversed with 1 month of insulin supplementation. In contrast, small doses of insulin initiated at the onset of diabetes result in renal hypertrophy and proportionate increases in GFR and RPF with a reduction in RT.

[1]  W. Keane,et al.  Intravascular and extracellular volumes in the diabetic rat. , 1981, Life sciences.

[2]  B. Brenner,et al.  Glomerular hemodynamics in experimental diabetes mellitus. , 1981, Kidney international.

[3]  W. Keane,et al.  The effects of chronic mesangial immune injury on glomerular function. , 1980, The Journal of laboratory and clinical medicine.

[4]  C. W. Gottschalk,et al.  Glomerular ultrafiltration dynamics: euvolemic and plasma volume-expanded rats. , 1980, The American journal of physiology.

[5]  H. Bohlen,et al.  Early arteriolar disturbances following streptozotocin-induced diabetes mellitus in adult mice. , 1980, Microvascular research.

[6]  M. Steffes,et al.  Amelioration of Mesangial Volume and Surface Alterations Following Islet Transplantation in Diabetic Rats , 1980, Diabetes.

[7]  J. White,et al.  Alteration in the balance of prostaglandin and thromboxane synthesis in diabetic rats. , 1980, The Journal of laboratory and clinical medicine.

[8]  B. Myers,et al.  Proteinuria and functional characteristics of the glomerular barrier in diabetic nephropathy. , 1980, Kidney international.

[9]  B. Brenner,et al.  Mechanism of reduced glomerular filtration rate in chronic malnutrition. , 1980, The Journal of clinical investigation.

[10]  Viberti Gc,et al.  Early functional and morphological changes in diabetic nephropathy. , 1979, Clinical Nephrology.

[11]  N. Wong,et al.  Acute effects of streptozotocin diabetes on rat renal function. , 1979, The Journal of laboratory and clinical medicine.

[12]  B. Brenner,et al.  Dynamics of Glomerular Ultrafiltration in Euvolemic Munich-Wistar Rats , 1978 .

[13]  A. Michael,et al.  Unilateral Shwartzman reaction: cortical necrosis in one kidney following in vivo perfusion with endotoxin. , 1977, Kidney international.

[14]  M. A. Johnson,et al.  Single-nephron pressures, flows, and resistances in hypertensive kidneys with nephrosclerosis. , 1977, Kidney international.

[15]  Mogensen Ce Renal function changes in diabetes. , 1976 .

[16]  A. Michael,et al.  Studies of diabetic nephropathy in animals and man. , 1976, Diabetes.

[17]  Bauer Jh,et al.  Volume studies. II. Simultaneous determination of plasma volume, red cell mass, extracellular fluid, and total body water before and after volume expansion in dog and man. , 1975 .

[18]  R. Burt,et al.  Simultaneous determination of extracellular fluid and total body water. I. , 1975, The Journal of laboratory and clinical medicine.

[19]  L. Lindbom,et al.  Kinetics of the glomerular ultrafiltration in the rat kidney. An experimental study. , 1975, Acta physiologica Scandinavica.

[20]  J. Assal,et al.  Plasma Renin Activity and Blood Volume in Uncontrolled Diabetes: Ketoacidosis, a State of Secondary Aldosteronism , 1975, Diabetes.

[21]  E. Hägg Renal lesions in rats with long-term alloxan diabetes. A semiquantitative light microscopic study with particular reference to the glomeruli. , 2009, Acta pathologica et microbiologica Scandinavica. Section A, Pathology.

[22]  A. R. Christlieb,et al.  Renin, Angiotensin, and Norepinephrine in Alloxan Diabetes , 1974, Diabetes.

[23]  C. Mogensen,et al.  Increased Kidney Size and Glomerular Filtration Rate in Early Juvenile Diabetes , 1973, Diabetes.

[24]  A. Michael,et al.  Spontaneous immunoglobulin and complement deposition in glomeruli of diabetic rats. , 1972, Laboratory investigation; a journal of technical methods and pathology.

[25]  B. Brenner,et al.  A model of glomerular ultrafiltration in the rat. , 1972, The American journal of physiology.

[26]  C. W. Gottschalk,et al.  Hydrostatic pressure in the rat kidney. , 1972, The American journal of physiology.

[27]  R. Blantz,et al.  Relation of distal tubular NaCl delivery and glomerular hydrostatic pressure. , 1972, Kidney international.

[28]  C. Mogensen Kidney function and glomerular permeability to macromolecules in early juvenile diabetes. , 1971, Scandinavian journal of clinical and laboratory investigation.

[29]  H. Friederici,et al.  Cortical Sponge Kidneys Induced in Rats by Alloxan , 1970, Diabetes.

[30]  B. Brenner,et al.  The relationship between peritubular capillary protein concentration and fluid reabsorption by the renal proximal tubule. , 1969, The Journal of clinical investigation.

[31]  Olsen Ts Diabetic glomerulosclerosis: a comparison between human and experimental lesions. , 1969 .

[32]  G. W. Snedecor STATISTICAL METHODS , 1967 .