Gender-Dimorphic Regulation of Skeletal Muscle Proteins in Streptozotocin-Induced Diabetic Rats

被引:19
作者
Choi, Minji [1 ]
Choi, Jung-Won [1 ]
Chaudhari, Harmesh N. [1 ]
Aseer, Kanikkai Raja [1 ]
Mukherjee, Rajib [1 ]
Yun, Jong Won [1 ]
机构
[1] Daegu Univ, Dept Biotechnol, Kyungsan 712714, Kyungbuk, South Korea
基金
新加坡国家研究基金会;
关键词
2-DE; Diabetes; Gender differences; Muscle proteome; Streptozotocin; HIGH-FAT-DIET; GLYCOGEN-PHOSPHORYLASE; INSULIN SENSITIVITY; EXPRESSION; INHIBITION; INDUCTION; ESTROGENS; PROTEOME; MELLITUS; CELLS;
D O I
10.1159/000343378
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Despite the fact that sexual differences increase diabetic risk and contribute to the need for gender-specific care, there remain contradictory results as to whether or not sexual dimorphism increases susceptibility to the development of type 1 diabetes mellitus. Methods: To examine gender-dimorphic regulation of skeletal muscle proteins between healthy control and STZ-induced diabetic rats of both genders, we performed differential proteome analysis using two-dimensional electrophoresis combined with mass spectrometry. Results: Animal experiments revealed that STZ treatment rendered female rats more susceptible to induction of diabetes than their male littermates with significantly lower plasma insulin levels due to hormonal regulation. Proteomic analysis of skeletal muscle identified a total of 21 proteins showing gender-dimorphic differential expression patterns between healthy controls and diabetic rats. Most interestingly, gender-specific proteome comparison showed that male and female rats displayed differential regulation of proteins involved in muscle contraction, carbohydrate, and lipid metabolism, as well as oxidative phosphorylation and cellular stress. Conclusion: The current proteomic study revealed that impaired protein regulation was more prominent in the muscle tissue of female diabetic rats, which were more susceptible to STZ-induced diabetes. We expect that the present proteomic data can provide valuable information for evidence-based gender-specific treatment of diabetes. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:408 / 420
页数:13
相关论文
共 52 条
[1]   Exercise training modulates heat shock protein response in diabetic rats [J].
Atalay, M ;
Oksala, NKJ ;
Laaksonen, DE ;
Khanna, S ;
Nakao, C ;
Lappalainen, J ;
Roy, S ;
Hänninen, O ;
Sen, CK .
JOURNAL OF APPLIED PHYSIOLOGY, 2004, 97 (02) :605-611
[2]   Gender-specific care of diabetes mellitus: particular considerations in the management of diabetic women [J].
Auryan, Szalat ;
Itamar, Raz .
DIABETES OBESITY & METABOLISM, 2008, 10 (12) :1135-1156
[3]   Glycogen phosphorylase inhibition in type 2 diabetes therapy - A systematic evaluation of metabolic and functional effects in rat skeletal muscle [J].
Baker, DJ ;
Timmons, JA ;
Greenhaff, PL .
DIABETES, 2005, 54 (08) :2453-2459
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   PARTIAL PURIFICATION AND PROPERTIES OF ATP - GMP PHOSPHOTRANSFERASE FROM RAT LIVER [J].
BUCCINO, RJ ;
ROTH, JS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1969, 132 (01) :49-&
[6]   Skeletal muscle and liver oxidative metabolism in response to a voluntary isocaloric intake of a high fat diet in male and female rats [J].
Catala-Niell, Antoni ;
Estrany, Maria Elena ;
Proenza, Ana Maria ;
Gianotti, Magdalena ;
Llado, Isabel .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2008, 22 (1-4) :327-336
[7]   Skeletal muscle myosin heavy chain synthesis in type 1 diabetes [J].
Charlton, MR ;
Balagopal, P ;
Nair, KS .
DIABETES, 1997, 46 (08) :1336-1340
[8]   Gender differences in skeletal muscle fatigability are related to contraction type and EMG spectral compression [J].
Clark, BC ;
Manini, TM ;
Thé, DJ ;
Doldo, NA ;
Ploutz-Snyder, LL .
JOURNAL OF APPLIED PHYSIOLOGY, 2003, 94 (06) :2263-2272
[9]   Skeletal muscle of female rats exhibit higher mitochondrial mass and oxidative-phosphorylative capacities compared to males [J].
Colom, Bartomeu ;
Alcolea, Maria Pilar ;
Valle, Adamo ;
Oliver, Jordi ;
Roca, Pilar ;
Garcia-Palmer, Francisco J. .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2007, 19 (1-4) :205-212
[10]   α-Enolase, a Multifunctional Protein: Its Role on Pathophysiological Situations [J].
Diaz-Ramos, Angels ;
Roig-Borrellas, Anna ;
Garcia-Melero, Ana ;
Lopez-Alemany, Roser .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2012,