Hindlimb unloading decreases thioredoxin-related antioxidant proteins and increases thioredoxin-binding protein-2 in rat skeletal muscle

被引:14
作者
Matsushima, Yasuyuki [1 ]
Nanri, Hiroki
Nara, Soichiro
Okufuji, Tatsuya
Ohta, Masanori
Hachisuka, Kenji
Ikeda, Masaharu
机构
[1] Univ Occupat & Environm Hlth, Dept Rehabil Med, Yahatanishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[2] Univ Occupat & Environm Hlth, Dept Hlth Dev, Yahatanishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[3] Seinan Jogakuin Univ, Dept Nutr Sci, Kitakyushu, Fukuoka 8030835, Japan
关键词
oxidative stress; antioxidant defense system; thioredoxin-1; peroxiredoxin-3/SP-22; thioredoxin-binding protein-2/vitamin D3 up-regulated protein 1;
D O I
10.1080/10715760600580488
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To investigate role(s) of thioredoxin-related antioxidant proteins in disuse muscle atrophy, we examined the levels of thioredoxin-1 (Trx-1), peroxiredoxin-3/SP-22 (Prx-3) and thioredoxin-binding protein-2 (TBP-2) in rat soleus muscle subjected to hindlimb unloading (HU) for 2, 4, 7 or 14 days. The muscle weight loss was initially observed on day 4. The increases in aclorein- and malondialdehyde-modified proteins, and the decreases in the levels of Trx-1, Prx-3 and Mn-SOD were observed in the late phase of muscle atrophy, whereas, the increase in mRNA expression of TBP-2, a negative regulator of thioredoxin, preceded muscle atrophy. These findings suggest that the decrease of those antioxidant proteins, particularly a marked decrease of Trx-1, may be responsible for the enhanced oxidative damage during the late phase of disuse muscle atrophy. Furthermore, the increase in TBP-2 preceding the muscle atrophy may suppress the thioredoxin-mediated redox signaling, which can be an initial trigger leading to disuse muscle atrophy.
引用
收藏
页码:715 / 722
页数:8
相关论文
共 42 条
[1]  
Appell HJ, 1997, INT J SPORTS MED, V18, P157
[2]   Antioxidant function of the mitochondrial protein SP-22 in the cardiovascular system [J].
Araki, M ;
Nanri, H ;
Ejima, K ;
Murasato, Y ;
Fujiwara, T ;
Nakashima, Y ;
Ikeda, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2271-2278
[3]  
CHAE HZ, 1994, J BIOL CHEM, V269, P27670
[4]   ISOLATION AND CHARACTERIZATION OF A NOVEL CDNA FROM HL-60 CELLS TREATED WITH 1,25-DIHYDROXYVITAMIN D-3 [J].
CHEN, KS ;
DELUCA, HF .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1994, 1219 (01) :26-32
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]  
DAVIES KJA, 1987, J BIOL CHEM, V262, P9895
[7]   Localization of thioredoxin reductase and thioredoxin in normal human placenta and their protective effect against oxidative stress [J].
Ejima, K ;
Nanri, H ;
Toki, N ;
Kashimura, M ;
Ikeda, M .
PLACENTA, 1999, 20 (01) :95-101
[8]   THIOREDOXIN REGENERATES PROTEINS INACTIVATED BY OXIDATIVE STRESS IN ENDOTHELIAL-CELLS [J].
FERNANDO, MR ;
NANRI, H ;
YOSHITAKE, S ;
NAGATAKUNO, K ;
MINAKAMI, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 209 (03) :917-922
[9]   THE EFFECT OF HYPOKINESIA AND HYPODYNAMIA ON PROTEIN-TURNOVER AND THE GROWTH OF 4 SKELETAL-MUSCLES OF THE RAT [J].
GOLDSPINK, DF ;
MORTON, AJ ;
LOUGHNA, P ;
GOLDSPINK, G .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1986, 407 (03) :333-340
[10]   Disuse muscle atrophy of lower limbs in hemiplegic patients [J].
Hachisuka, KJ ;
Umezu, YC ;
Ogata, HJ .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 1997, 78 (01) :13-18