Ranirestat (AS-3201), a potent aldose reductase inhibitor, reduces sorbitol levels and improves motor nerve conduction velocity in streptozotocin-diabetic rats

被引:38
作者
Matsumoto, Takafumi [1 ,2 ]
Ono, Yoshiyuki [3 ]
Kurono, Masuo [4 ]
Kuromiya, Akemi
Nakamura, Keiji [5 ]
Bril, Vera [6 ]
机构
[1] Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
[2] Dainippon Sumitomo Pharma Co Ltd, Genom Sci Labs, Konohana Ku, Osaka 5540022, Japan
[3] Dainippon Sumitomo Pharma Co Ltd, Int Business Management, Fukushima Ku, Osaka 5530001, Japan
[4] Dainippon Sumitomo Pharma Co Ltd, Chem Res Labs, Osaka 5640053, Japan
[5] Nichiei Sangyo Co Ltd, Ctr Analyt Chem, Osaka 5640053, Japan
[6] Univ Toronto, Toronto Gen Hosp, Dept Med, Toronto, ON M5G 2C4, Canada
关键词
aldose reductase inhibitor; ranirestat (AS-3201); polyol pathway; motor nerve conduction velocity; streptozotocin-diabetic rat;
D O I
10.1254/jphs.08061FP
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ranirestat (AS-3201) is a novel aldose reductase (AR) inhibitor with potentially beneficial effects on diabetic sensorimotor polyneuropathy. In this study, we performed a kinetic analysis to determine the mode of inhibition of ranirestat on AR and investigated the effects of ranirestat on sorbitol levels in the sciatic nerves and lens of streptozotocin (STZ)-diabetic rats. We also evaluated the effects on motor nerve conduction velocity (MNCV) in STZ-diabetic rats. Kinetic analyses revealed that the ranirestat inhibition of AR is uncompetitive and reversible. In the sciatic nerve and lens of STZ-diabetic rats, single oral administration of ranirestat slightly reduced sorbitol levels. However, repeated oral administration of ranirestat for 5, 21, or 60 days enhanced the reducing effect of the ranirestat on sorbitol levels in the sciatic nerves and lens of STZ-diabetic rats with maximum effects after 21 days of treatment. Finally, repeated oral administration of ranirestat for 21 or 42 days dose-dependently improved the STZ-induced decrease in MNCV in STZ-diabetic rats. These findings demonstrate that repeated oral administration of ranirestat reduces sorbitol accumulation and improves NMCV in STZ-diabetic rats, indicating that ranirestat is an agent for the management of diabetic sensorimotor polyneuropathy.
引用
收藏
页码:231 / 237
页数:7
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