Hyperglycemia Inhibits Recovery From Disuse-Induced Skeletal Muscle Atrophy in Rats

被引:8
作者
Kataoka, H. [1 ,2 ]
Nakano, J. [3 ]
Morimoto, Y. [1 ,4 ]
Honda, Y. [1 ,4 ]
Sakamoto, J. [3 ]
Origuchi, T. [1 ]
Okita, M. [1 ]
Yoshimura, T. [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Locomot Rehabil Sci, Unit Rehabil Sci, Nagasaki, Japan
[2] Nagasaki Mem Hosp, Dept Rehabil, Nagasaki, Japan
[3] Nagasaki Univ, Grad Sch Biomed Sci, Unit Phys Therapy & Occupat Therapy Sci, 1-7-1 Sakamoto, Nagasaki, Japan
[4] Nagasaki Univ Hosp, Dept Rehabil, Nagasaki, Japan
关键词
Hyperglycemia; Disuse-induced muscle atrophy; Recovery; DIABETES-MELLITUS; GROWTH-FACTOR; TIME-COURSE; FIBER-TYPE; ANGIOGENESIS; CAPILLARIZATION; REGENERATION; EXPRESSION; PROMOTES; EXERCISE;
D O I
10.33549/physiolres.932687
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The purpose of this study was to evaluate the effects of hyperglycemia on skeletal muscle recovery following disuse-induced muscle atrophy in rats. Wistar rats were grouped as streptozotocin-induced diabetic rats and non-diabetic rats. Both ankle joints of each rat were immobilized to induce atrophy of the gastrocnemius muscles. After two weeks of immobilization and an additional two weeks of recovery, tail blood and gastrocnemius muscles were isolated. Serial cross sections of muscles were stained for myosin ATPase (pH 4.5) and alkaline phosphatase activity. Serum insulin and muscle insulin-like growth factor-1 (IGF-1) levels were also measured. Serum insulin levels were significantly reduced in the diabetic rats compared to the non-diabetic controls. The diameters of type I, IIa, and IIb myofibers and capillary-to-myofiber ratio in the isolated muscle tissue were decreased after immobilization in both treatments. During the recovery period, these parameters were restored in the non-diabetic rats, but not in the diabetic rats. In addition, muscle IGF-1 levels after recovery increased significantly in the non-diabetic rats, but not in the diabetic rats. We conclude that decreased levels of insulin and IGF-1 and impairment of angiogenesis associated with diabetes might be partly responsible for the inhibition of regrowth in diabetic muscle.
引用
收藏
页码:465 / 474
页数:10
相关论文
共 32 条
[1]   Time course of changes in markers of myogenesis in overloaded rat skeletal muscles [J].
Adams, GR ;
Haddad, F ;
Baldwin, KM .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 87 (05) :1705-1712
[2]   ARREST OF DEVELOPMENTAL CONVERSION OF TYPE-II TO TYPE-I FIBERS AFTER SUSPENSION HYPOKINESIA [J].
ASMUSSEN, G ;
SOUKUP, T .
HISTOCHEMICAL JOURNAL, 1991, 23 (07) :312-322
[3]   The pathobiology of diabetic complications - A unifying mechanism [J].
Brownlee, M .
DIABETES, 2005, 54 (06) :1615-1625
[4]   Single-fiber and whole muscle analyses of MHC isoform plasticity: interaction between T-3 and unloading [J].
Caiozzo, VJ ;
Baker, MJ ;
McCue, SA ;
Baldwin, KM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 273 (03) :C944-C952
[5]   Pressure Hyperalgesia in Hind Limb Suspended Rats [J].
Chowdhury, Parimal ;
Soulsby, Michael E. ;
Jayroe, John ;
Akel, Nisreen S. ;
Gaddy, Dana ;
Dobretsov, Maxim .
AVIATION SPACE AND ENVIRONMENTAL MEDICINE, 2011, 82 (10) :988-991
[6]   Role of the insulin-like growth factor I decline in the induction of atrogin-1/MAFbx during fasting and diabetes [J].
Dehoux, M ;
Van Beneden, R ;
Pasko, N ;
Lause, P ;
Verniers, J ;
Underwood, L ;
Ketelslegers, JM ;
Thissen, JP .
ENDOCRINOLOGY, 2004, 145 (11) :4806-4812
[7]   Composition and size of type I, IIA, IID/X, and IIB fibers and citrate synthase activity of rat muscle [J].
Delp, MD ;
Duan, CP .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 80 (01) :261-270
[8]   RESTORATION OF ANGIOGENESIS BY ENALAPRIL IN DIABETIC HINDLIMB ISCHEMC RATS [J].
Fallahzadeh, Ali Reza ;
Khazaei, Majid ;
Sharifi, Mohammad Reza .
BIOMEDICAL PAPERS-OLOMOUC, 2011, 155 (02) :137-142
[9]   Severe diabetes prohibits elevations in muscle protein synthesis after acute resistance exercise in rats [J].
Fedele, MJ ;
Hernandez, JM ;
Lang, CH ;
Vary, TC ;
Kimball, SR ;
Jefferson, LS ;
Farrell, PA .
JOURNAL OF APPLIED PHYSIOLOGY, 2000, 88 (01) :102-108
[10]   Molecular and biological properties of vascular endothelial growth factor [J].
Ferrara, N .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (07) :527-543