The radical scavenger edaravone counteracts diabetes in multiple low-dose streptozotocin-treated mice

被引:38
作者
Fukudome, Daisuke [1 ]
Matsuda, Maki [1 ]
Kawasaki, Toshiyuki [1 ]
Ago, Yukio [1 ]
Matsuda, Toshio [1 ]
机构
[1] Osaka Univ, Lab Med Pharmacol, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan
关键词
edaravone; multiple low-dose streptozotocin; diabetes; insulitis; thiobarbituric acid reactive substance;
D O I
10.1016/j.ejphar.2008.01.033
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Edaravone is a potent scavenger of hydroxyl radicals and attenuates oxidative damage-related neurodegenerative diseases. Previous studies suggest that oxidative stress plays a key role in the pathogenesis of diabetes. The present study examined the effect of edaravone on diabetes in multiple low-dose streptozotocin-treated mice. Mice treated with low-doses of streptozotocin for five consecutive days showed progressive hyperglycemia and an increased incidence of diabetes. Daily treatment with edaravone during the streptozotocin injections counteracted the multiple low-dose streptozotocin-induced hyperglycemia in a dose-dependent manner. Edaravone protected against the multiple low-dose streptozotocin-induced reduction in pancreatic insulin. The suppressive effects of edaravone were also observed when it was administered after the last injection of streptozotocin. Histochemical examination showed that multiple low-dose streptozotocin treatment caused mononuclear cell infiltration in pancreatic islets, followed by hyperglycemia, and that edaravone significantly inhibited the multiple low-dose streptozotocin-induced insulitis. Multiple low-dose streptozotocin treatment also increased the lipid peroxidation product thiobarbituric acid reactive substance in pancreatic tissues of mice, and this effect was completely inhibited by edaravone. These findings suggest that edaravone, even after streptozotocin treatment, counteracts the development of multiple low-dose streptozotocin-induced diabetes by scavenging free radicals, which are possible mediators of the immune destruction of islet beta cells. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 169
页数:6
相关论文
共 47 条
[1]   Cytokine-induced inhibition of insulin release from mouse pancreatic β-cells deficient in inducible nitric oxide synthase [J].
Andersson, AK ;
Flodström, M ;
Sandler, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 281 (02) :396-403
[2]  
Araki Y, 2003, INT J MOL MED, V12, P121
[3]   Overexpression of metallothionein in pancreatic β-cells reduces streptozotocin-induced DNA damage and diabetes [J].
Chen, HN ;
Carlson, EC ;
Pellet, L ;
Moritz, JT ;
Epstein, PN .
DIABETES, 2001, 50 (09) :2040-2046
[4]   DOES NITRIC-OXIDE MEDIATE AUTOIMMUNE DESTRUCTION OF BETA-CELLS - POSSIBLE THERAPEUTIC INTERVENTIONS IN IDDM [J].
CORBETT, JA ;
MCDANIEL, ML .
DIABETES, 1992, 41 (08) :897-903
[5]  
Eizirik DL, 1997, DIABETES METAB REV, V13, P293, DOI 10.1002/(SICI)1099-0895(199712)13:4<293::AID-DMR195>3.3.CO
[6]  
2-W
[7]   Reduced sensitivity of inducible nitric oxide synthase-deficient mice to multiple low-dose streptozotocin-induced diabetes [J].
Flodström, M ;
Tyrberg, B ;
Eizirik, DL ;
Sandler, S .
DIABETES, 1999, 48 (04) :706-713
[8]   Efficacy of edaravone, a free radical scavenger, on left ventricular function and structure in diabetes mellitus [J].
Hayashi, T ;
Mori, T ;
Sohmiya, K ;
Okada, Y ;
Inamoto, S ;
Okuda, N ;
Mori, H ;
Kitaura, Y .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2003, 41 (06) :923-929
[9]   ANTIOXIDANT MDL 29,311 PREVENTS DIABETES IN NONOBESE DIABETIC AND MULTIPLE LOW-DOSE STZ-INJECTED MICE [J].
HEINEKE, EW ;
JOHNSON, MB ;
DILLBERGER, JE ;
ROBINSON, KM .
DIABETES, 1993, 42 (12) :1721-1730
[10]   AMINOGUANIDINE, AN INHIBITOR OF NITRIC-OXIDE FORMATION, FAILS TO PROTECT AGAINST INSULITIS AND HYPERGLYCEMIA-INDUCED BY MULTIPLE LOW-DOSE STREPTOZOTOCIN INJECTIONS IN MICE [J].
HOLSTAD, M ;
SANDLER, S .
AUTOIMMUNITY, 1993, 15 (04) :311-314