Glomerular selective permeability to macromolecular neutral dextrans in experimental diabetes. 1981

J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie

Rats with streptozotocin-induced chronic diabetes mellitus develop a glomerulopathy functionally manifested by proteinuria. The ability of the glomerular capillary wall to retard filtration of macromolecules was examined in 5 chronically diabetic Munich-Wistar rats exhibiting excessive proteinuria (39 +/- 7 mg/24 h, mean +/- SEM) and 5 age-matched normal Munich-Wistar rats without increased proteinuria (4.7 +/- 0.2 mg/24 h). Urinary albumin excretion was not increased in the diabetic rats (2.0 +/- 0.6 mg/24 h vs 1.6 +/- 0.3 mg/24 h) suggesting that the normal net electronegative charge of the glomerular capillary wall was not altered. Fractional clearances of macromolecular neutral dextrans were similar in diabetic and normal rats throughout a wide range of molecular size (18-42 A). Glomerular filtration rate was the same in the two groups of rats (2.77 +/- 0.16 ml/min in diabetics and 2.72 +/- 0.11 ml/min in normals) suggesting that renal haemodynamic factors did not influence fractional clearances of neutral dextrans in diabetic rats. We conclude that the proteinuria exhibited by these chronically diabetic rats is not attributable to alterations of size-selective properties of the glomerular capillary wall, such as increases in the size or the number of pores.

UI MeSH Term Description Entries
D007678 Kidney Glomerulus A cluster of convoluted capillaries beginning at each nephric tubule in the kidney and held together by connective tissue. Glomerulus, Kidney
D008970 Molecular Weight The sum of the weight of all the atoms in a molecule. Molecular Weights,Weight, Molecular,Weights, Molecular
D010539 Permeability Property of membranes and other structures to permit passage of light, heat, gases, liquids, metabolites, and mineral ions. Permeabilities
D011507 Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. Proteinurias
D002236 Carbohydrate Conformation The characteristic 3-dimensional shape of a carbohydrate. Carbohydrate Linkage,Carbohydrate Conformations,Carbohydrate Linkages,Conformation, Carbohydrate,Conformations, Carbohydrate,Linkage, Carbohydrate,Linkages, Carbohydrate
D003911 Dextrans A group of glucose polymers made by certain bacteria. Dextrans are used therapeutically as plasma volume expanders and anticoagulants. They are also commonly used in biological experimentation and in industry for a wide variety of purposes. Dextran,Dextran 40,Dextran 40000,Dextran 70,Dextran 75,Dextran 80,Dextran B-1355,Dextran B-1355-S,Dextran B1355,Dextran B512,Dextran Derivatives,Dextran M 70,Dextran T 70,Dextran T-40,Dextran T-500,Hemodex,Hyskon,Infukoll,Macrodex,Polyglucin,Promit,Rheodextran,Rheoisodex,Rheomacrodex,Rheopolyglucin,Rondex,Saviosol,Dextran B 1355,Dextran B 1355 S,Dextran T 40,Dextran T 500
D003921 Diabetes Mellitus, Experimental Diabetes mellitus induced experimentally by administration of various diabetogenic agents or by PANCREATECTOMY. Alloxan Diabetes,Streptozocin Diabetes,Streptozotocin Diabetes,Experimental Diabetes Mellitus,Diabete, Streptozocin,Diabetes, Alloxan,Diabetes, Streptozocin,Diabetes, Streptozotocin,Streptozocin Diabete
D005260 Female Females
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001692 Biological Transport The movement of materials (including biochemical substances and drugs) through a biological system at the cellular level. The transport can be across cell membranes and epithelial layers. It also can occur within intracellular compartments and extracellular compartments. Transport, Biological,Biologic Transport,Transport, Biologic

Related Publications

J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
May 1982, Kidney international,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
August 1976, The American journal of physiology,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
October 1983, The American journal of physiology,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
February 1968, Clinical science,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
February 1996, The American journal of physiology,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
July 1975, The Journal of experimental medicine,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
January 1964, Verhandlungen der Deutschen Gesellschaft fur Innere Medizin,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
July 1990, The American journal of physiology,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
January 1970, Clinical science,
J P Pennell, and N Yanagawa, and K H Hwang, and M M Millard, and J J Bourgoignie
March 1969, Transplantation proceedings,
Copied contents to your clipboard!