Influence of short-term L-arginine supplementation on carbohydrate balance in rats with ischemia-reperfusion syndrome

被引:5
作者
Krauss, Hanna [2 ]
Bogdanski, Pawel [3 ]
Sosnowski, Przemyslaw [2 ]
Suliburska, Joanna [1 ]
Jablecka, Anna [4 ]
Jastak, Rafal [2 ]
Sassek, Maciej [5 ]
Mackowiak, Pawel [5 ]
Cieslewicz, Artur [4 ]
Pupek-Musialik, Danuta [3 ]
机构
[1] Poznan Univ Life Sci, Dept Hyg & Human Nutr, PL-60624 Poznan, Poland
[2] Poznan Univ Med Sci, Dept Physiol, PL-60781 Poznan, Poland
[3] Poznan Univ Med Sci, Dept Internal Med Metab Disorders & Hypertens, PL-60569 Poznan, Poland
[4] Poznan Univ Med Sci, Dept Clin Pharmacol, PL-61848 Poznan, Poland
[5] Poznan Univ Life Sci, Dept Physiol & Biochem, Fac Anim Breeding & Biol, PL-60637 Poznan, Poland
关键词
L-arginine; ischemia; insulin; glucose; INSULIN-RECEPTOR SUBSTRATE-1; NITRIC-OXIDE SYNTHASES; SKELETAL-MUSCLE; AMINO-ACID; ENDOTHELIAL DYSFUNCTION; MTOR; BINDING; PHOSPHORYLATION; RESISTANCE; CELLS;
D O I
10.1016/S1734-1140(12)70859-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: There are studies showing stimulative effect of arginine on insulin secretion. This mechanism is not fully explained. The effects of the impact of arginine on carbohydrate balance under the conditions of ischemia and reperfusion remain to be determined. The aim of this study is the evaluation of the influence of short-term L-arginine supplementation on the concentration of glucose and insulin in blood and insulin binding in rat skeletal muscle under the conditions of ischemia and reperfusion. Methods: The study was conducted on male Wistar rats with average body mass 250 +/- 30g. Animals were divided into four groups: Group I - control, Group II - placebo, Group III - L-arginine 500 mg/kg/24 h for 5 days, Group IV - L-arginine and L-NAME (75 mu mol/rat/24 h) for 5 days. Each group was divided into subgroups depending on duration of ischemia and reperfusion. Acute ischemia of hind limb was induced in each group by putting pneumatic tourniquet on the thigh. Blood samples and skeletal muscles were collected from the rats. Plasma concentrations of glucose and insulin were measured. Insulin binding to insulin receptors was determined in skeletal muscle. Results: A clear reduction of insulin binding to receptor was found in the group of animals without ischemia and the group supplemented with L-arginine and subjected to 4-h ischemia and 30- and 120-min reperfusion. A significant increase in insulin level was found in groups of animals with L-arginine and/or L-NAME subjected to 4-h ischemia at all times of reperfusion. Supplementation with L-arginine and/or L-NAME decreased levels of glucose in blood scrum of animals undergoing ischemia-reperfusion syndrome compared to the control and placebo groups. Conclusion: Under conditions of ischemia-reperfusion, short-term administration of L-arginine causes a decrease in insulin binding capacity of insulin receptors in skeletal muscle, an increase in insulin level and a decrease in the concentration of glucose in blood serum.
引用
收藏
页码:635 / 642
页数:8
相关论文
共 34 条
[1]  
ANTONIOLI JA, 1969, J BIOL CHEM, V244, P1505
[2]   Prevention of Renal Injury and Endothelial Dysfunction by Chronic L-Arginine and Antioxidant Treatment [J].
Arellano-Mendoza, Monica G. ;
Vargas-Robles, Hilda ;
Del Valle-Mondragon, Leonardo ;
Rios, Amelia ;
Escalante, Bruno .
RENAL FAILURE, 2011, 33 (01) :47-53
[3]   Arginine-induced stimulation of protein synthesis and survival in IPEC-J2 cells is mediated by mTOR but not nitric oxide [J].
Bauchart-Thevret, Caroline ;
Cui, Liwei ;
Wu, Guoyao ;
Burrin, Douglas G. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2010, 299 (06) :E899-E909
[4]   Tsc tumour suppressor proteins antagonize amino-acid-TOR signalling [J].
Gao, XS ;
Zhang, Y ;
Arrazola, P ;
Hino, O ;
Kobayashi, T ;
Yeung, RS ;
Ru, BG ;
Pan, DJ .
NATURE CELL BIOLOGY, 2002, 4 (09) :699-704
[5]   DOWN-REGULATION OF INSULIN-RECEPTORS IS RELATED TO INSULIN INTERNALIZATION [J].
GEIGER, D ;
CARPENTIER, JL ;
GORDEN, P ;
ORCI, L .
EXPERIMENTAL CELL RESEARCH, 1989, 185 (01) :33-40
[6]   INSULIN RECEPTORS ARE WIDELY DISTRIBUTED IN CENTRAL NERVOUS-SYSTEM OF RAT [J].
HAVRANKOVA, J ;
ROTH, J .
NATURE, 1978, 272 (5656) :827-829
[7]   Upstream and downstream of mTOR [J].
Hay, N ;
Sonenberg, N .
GENES & DEVELOPMENT, 2004, 18 (16) :1926-1945
[8]   TSC2 mediates cellular energy response to control cell growth and survival [J].
Inoki, K ;
Zhu, TQ ;
Guan, KL .
CELL, 2003, 115 (05) :577-590
[9]   SUPPRESSION BY HIGH GLUCOSE-CONCENTRATION OF INSULIN-RECEPTOR UP-REGULATION IN DIAPHRAGM AND FLEXOR DIGITORUM BREVIS MUSCLES FROM DIABETIC KK-CA(Y) AND STREPTOZOTOCIN-DIABETIC MICE [J].
KOBAYASHI, S ;
NAITOH, T ;
NAKADATE, T ;
KIMURA, I ;
KIMURA, M .
JOURNAL OF PHARMACOBIO-DYNAMICS, 1992, 15 (04) :175-180
[10]   Amino acid-dependent modulation of glucose metabolism in humans [J].
Krebs, M .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2005, 35 (06) :351-354