Diabetes, Vol 46, Issue 1 94-106, Copyright © 1997 by American Diabetes Association
Discordant effects of guanidines on renal structure and function and on regional vascular dysfunction and collagen changes in diabetic rats
JR Nyengaard, K Chang, S Berhorst, KM Reiser, JR Williamson and RG Tilton
Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
We examined the effects of aminoguanidine and methylguanidine on vascular
dysfunction, glomerular structural changes, and indexes of early and late
nonenzymatic glycation in 7-month streptozotocin-induced diabetic rats.
Kidney weight, glomerular volume, fractional mesangial volume, glomerular
capillary basement membrane width, and urinary albumin excretion were
increased in diabetic rats. Diabetes also 1) increased vascular albumin
permeation twofold in retina, sciatic nerve, aorta, skin, and kidney; 2)
decreased renal collagenase-soluble collagen; 3) increased
collagen-associated fluorescence in kidney and skin but not in aorta; and
4) increased glycated hemoglobin levels and aortic pentosidine levels.
Aminoguanidine reduced albuminuria by 70% after 4 months, and both
guanidines 1) normalized aortic pentosidine levels and renal
collagenase-soluble collagen, 2) had no effect on glycated hemoglobin
levels or collagen-associated fluorescence (in aorta, kidney, or skin), and
3) had little or no effect on regional albumin permeation. These discordant
effects of aminoguanidine on diabetes-induced vascular changes versus
parameters of nonenzymatic glycation are consistent with a multifactorial
pathogenesis of diabetic complications, including roles for metabolic
imbalances independent of nonenzymatic glycation. To the extent that
glomerular matrix accumulation and increased regional albumin permeation in
chronically diabetic rats are sequelae of nonenzymatic glycation, these
findings point to an important role for early glycation reactions and
products.