Oxidative stress in the latissimus dorsi muscle of diabetic rats

被引:21
作者
De Angelis, KLD
Cestari, IA
Barp, J
Dall'Ago, P
Fernandes, TG
de Bittencourt, PIH
Belló-Klein, A
Belló, AA
Llesuy, S
Irigoyen, MC
机构
[1] Univ Sao Paulo, Fac Med, HC, Inst Coracao,Unidade Hipertensao, BR-05043000 Sao Paulo, Brazil
[2] Univ Sao Paulo, Fac Med, HC, Inst Coracao,Div Expt, BR-05043000 Sao Paulo, Brazil
[3] Univ Fed Rio Grande do Sul, Inst Ciencias Basicas Saude, Dept Fisiol, Lab Fisiol Cardiovasc, Porto Alegre, RS, Brazil
[4] Univ Sao Paulo, Fac Med, Inst Coracao, Div Bioengn, BR-05043000 Sao Paulo, Brazil
关键词
streptozotocin-diabetes; latissimus dorsi muscle; oxidative stress; catalase; glutathione;
D O I
10.1590/S0100-879X2000001100016
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The purpose of the present study was to investigate the effects of experimental diabetes on the oxidant and antioxidant status of latissimus dorsi (LD) muscles of male Wistar rats (220 +/- 5 g, N = 11). Shortterm (5 days) diabetes was induced by a single injection of streptozotocin (STZ, 50 mg/kg, iv; glycemia >300 mg/dl). LD muscle of STZ-diabetic rats presented higher levels of thiobarbituric acid reactive substances (TEARS) and chemiluminescence (0.36 +/- 0.02 nmol/mg protein and 14706 +/- 1581 cps/mg protein) than LD muscle of normal rats (0.23 +/- 0.04 nmol/mg protein and 7389 +/- 1355 cps/mg protein). Diabetes induced a 92% increase in catalase and a 27% increase in glutathione S-transferase activities in LD muscle. Glutathione peroxidase activity was reduced (58%) in STZ-diabetic rats and superoxide dismutase activity was similar in LD muscle of both groups. A positive correlation was obtained between catalase activity and the oxidative stress of LD, as evaluated in terms of TEARS (r = 0.78) and by chemiluminescence (r = 0.89). Catalase activity also correlated inversely with glutathione peroxidase activity (r = 0.79). These data suggest that an increased oxidative stress in LD muscle of diabetic rats may be related to skeletal muscle myopathy.
引用
收藏
页码:1363 / 1368
页数:6
相关论文
共 21 条
[1]
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]
Chemiluminescence and antioxidant levels during peroxisome proliferation by fenofibrate [J].
Arnaiz, SL ;
Travacio, M ;
Monserrat, AJ ;
Cutrin, JC ;
Llesuy, S ;
Boveris, A .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1997, 1360 (03) :222-228
[3]
ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[4]
Buege J A, 1978, Methods Enzymol, V52, P302
[5]
CHANGES IN SKELETAL-MUSCLE CONTRACTILE PROPERTIES IN STREPTOZOCIN-INDUCED DIABETIC RATS AND ROLE OF POLYOL PATHWAY AND HYPOINSULINEMIA [J].
CAMERON, NE ;
COTTER, MA ;
ROBERTSON, S .
DIABETES, 1990, 39 (04) :460-465
[6]
Metabolic and vascular factors in the pathogenesis of diabetic neuropathy [J].
Cameron, NE ;
Cotter, MA .
DIABETES, 1997, 46 :S31-S37
[7]
Dynamic cardiomyoplasty: clinical follow-up at 12 years [J].
Chachques, JC ;
Marino, JP ;
Lajos, P ;
Zegdi, R ;
DAttellis, N ;
Fornes, P ;
Fabiani, JN ;
Carpentier, A .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 1997, 12 (04) :560-567
[8]
CHRISTIE KN, 1979, J HISTOCHEM CYTOCHEM, V27, P814, DOI 10.1177/27.4.376691
[9]
D'Avila KP, 1997, ARTIF ORGANS, V2, P485
[10]
FLECHA BG, 1991, FREE RADICAL BIO MED, V10, P93