Abstract
Aminoguanidine inhibits the formation of advanced glycation end-products, and has
been extensively examined in animals. However, administration of aminoguanidine decreases
the hepatic content of pyridoxal phosphate. In order to avoid this problem, we developed
an aminoguanidine pyridoxal Schiff base adduct and examined its efficacy in vitro as well as in a model of diabetic nephropathy. Mice with streptozotocin-induced diabetes
were treated with aminoguanidine or aminoguanidine pyridoxal adduct for 9 weeks. An
in vitro study was also performed to assess the antioxidant activity of aminoguanidine and
its pyridoxal adduct. Neither drug altered glycemic control. Aminoguanidine pyridoxal
adduct significantly improved urinary albumin excretion by 78.1 % compared with the
diabetic control, and also had a better preventive effect on the progression of renal
pathology than aminoguanidine did. Inhibition of glycation by both drugs was similar,
but the antioxidant activity of the pyridoxal adduct was far superior. These findings
suggest that aminoguanidine pyridoxal adduct may be superior to aminoguanidine, as
it not only prevents vitamin B6 deficiency but is also better at controlling diabetic nephropathy, as this adduct
inhibits oxidation as well as glycation.
Key words
Aminoguanidine - Pyridoxal - Vitamin B6
- Glycation - Antioxidant - Nephropathy
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K. Yanagisawa, M.D., Ph.D.
Department of Internal Medicine II, Hokkaido University School of Medicine
Sapporo, 060-8638 · Japan
Phone: + 81 (11) 716 11 61 (Ex. 59 17)
Fax: + 81 (11) 706 77 10 ·
Email: kyanagi@med.hokudai.ac.jp