The roles of oxidative stress and antioxidant treatment in experimental diabetic neuropathy

被引:306
作者
Low, PA [1 ]
Nickander, KK [1 ]
Tritschler, HJ [1 ]
机构
[1] ASTA MED, FRANKFURT, GERMANY
关键词
D O I
10.2337/diab.46.2.S38
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oxidative stress is present in the diabetic state, Our work has focused on its presence in peripheral nerves, Antioxidant enzymes are reduced in peripheral nerves and are further reduced in diabetic nerves, That lipid peroxidation will cause neuropathy is supported by evidence of the development of neuropathy Be novo when normal nerves are rendered alpha-tocopherol deficient and by the augmentation of the conduction deficit in diabetic nerves subjected to this insult, Oxidative stress appears to be primarily due to the processes of nerve ischemia and hyperglycemia auto-oxidation. The indexes of oxidative stress include an increase in nerve, dorsal root, and sympathetic ganglia lipid hydroperoxides and conjugated dienes. The: most reliable and sensitive index, however is a reduction in reduced glutathione, Experimental diabetic neuropathy results in myelinopathy of dorsal roots and a vacuolar neuropathy of dorsal root ganglion. The vacuoles are mitochondrial; we posit that lipid peroxidation causes mitochondrial DNA mutations that increase reduced oxygen species, causing further damage to mitochondrial respiratory chain and function and resulting in a sensory neuropathy, alpha-lipoic acid is a potent antioxidant that prevents Lipid peroxidation in vitro and in vivo, We evaluated the efficacy of the drug in doses of 20, 50, and 100 mg/kg administered intraperitoneally in preventing the biochemical, electrophysiological, and nerve blood flow deficits in the peripheral nerves of experimental diabetic neuropathy, alpha-lipoic acid dose- and time-dependently prevented the deficits in nerve conduction and nerve blood flow and biochemical abnormalities (reductions in reduced glutathione and lipid peroxidation), The nerve blood flow deficit was 50% (P < 0.001), Supplementation dose-dependently prevented the deficit; at the highest concentration, nerve blood flow was not different from that of control nerves, Digital nerve conduction underwent; a dose-dependent improvement at 1 month (P < 0.05), By 3 months, all treated groups had lost their deficit, The antioxidant drug is potentially efficacious for human diabetic sensory neuropathy.
引用
收藏
页码:S38 / S42
页数:5
相关论文
共 43 条
[1]   ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[2]   POTENTIAL USE OF GLUTATHIONE FOR THE PREVENTION AND TREATMENT OF DIABETIC NEUROPATHY IN THE STREPTOZOTOCIN-INDUCED DIABETIC RAT [J].
BRAVENBOER, B ;
KAPPELLE, AC ;
HAMERS, FPT ;
VANBUREN, T ;
ERKELENS, DW ;
GISPEN, WH .
DIABETOLOGIA, 1992, 35 (09) :813-817
[3]  
BROWNLEE M, 1988, NEW ENGL J MED, V318, P1315
[4]  
BUSSE E, 1992, ARZNEIMITTELFORSCH, V42-1, P829
[5]   NERVE BLOOD-FLOW IN EARLY EXPERIMENTAL DIABETES IN RATS - RELATION TO CONDUCTION DEFICITS [J].
CAMERON, NE ;
COTTER, MA ;
LOW, PA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (01) :E1-E8
[6]   ANTIOXIDANT AND PROOXIDANT EFFECTS ON NERVE-CONDUCTION VELOCITY, ENDONEURIAL BLOOD-FLOW AND OXYGEN-TENSION IN NONDIABETIC AND STREPTOZOTOCIN-DIABETIC RATS [J].
CAMERON, NE ;
COTTER, MA ;
ARCHIBALD, V ;
DINES, KC ;
MAXFIELD, EK .
DIABETOLOGIA, 1994, 37 (05) :449-459
[7]   ANTIOXIDANT TREATMENT PREVENTS THE DEVELOPMENT OF PERIPHERAL-NERVE DYSFUNCTION IN STREPTOZOTOCIN-DIABETIC RATS [J].
CAMERON, NE ;
COTTER, MA ;
MAXFIELD, EK .
DIABETOLOGIA, 1993, 36 (04) :299-304
[8]   NEUROVASCULAR DYSFUNCTION IN DIABETIC RATS - POTENTIAL CONTRIBUTION OF AUTOXIDATION AND FREE-RADICALS EXAMINED USING TRANSITION-METAL CHELATING-AGENTS [J].
CAMERON, NE ;
COTTER, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (02) :1159-1163
[9]  
COTTER MA, 1995, N-S ARCH PHARMACOL, V351, P630
[10]   THIOCTIC ACID INDUCES DOSE-DEPENDENT SPROUTING OF NEURITES IN CULTURED RAT NEUROBLASTOMA-CELLS [J].
DIMPFEL, W ;
SPULER, M ;
PIERAU, FK ;
ULRICH, H .
DEVELOPMENTAL PHARMACOLOGY AND THERAPEUTICS, 1990, 14 (03) :193-199