Oxidative stress participates in the breakdown of neuronal phenotype in experimental diabetic neuropathy

Diabetologia

Volumn 44, Issue 4, 2001, Pages 424-428

  Hounsom, L ^a   Corder, R ^a   Patel, J ^a   Tomlinson, D R ^b  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

Diabetic neuropathy; Nerve conduction velocity; Nerve growth factor; Neuropeptide Y; Oxidative stress; Primaquine; Substance P; Vitamin E deficiency; lipoic acid; linolenic acid

Indexed keywords

ALPHA TOCOPHEROL; GAMMA LINOLENIC ACID; NERVE GROWTH FACTOR; NEUROPEPTIDE; NEUROPEPTIDE Y; PRIMAQUINE; STREPTOZOCIN; SUBSTANCE P; THIOCTIC ACID;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DIABETIC NEUROPATHY; MALE; MOTOR NERVE CONDUCTION; NERVE CELL; NONHUMAN; NUTRITIONAL DEFICIENCY; OXIDATIVE STRESS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; RAT; SCIATIC NERVE; SENSORY NERVE CONDUCTION;

ANIMALS; DIABETES MELLITUS, EXPERIMENTAL; DIABETIC NEUROPATHIES; GAMMA-LINOLENIC ACID; MALE; NERVE GROWTH FACTOR; NEURAL CONDUCTION; NEURONS; NEUROPEPTIDE Y; OXIDATIVE STRESS; PHENOTYPE; PRIMAQUINE; RATS; RATS, WISTAR; SCIATIC NERVE; SUBSTANCE P; THIOCTIC ACID; VITAMIN E;

EID: 0035054480     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001250051638     Document Type: Article

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