Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1α)PDH gene expression in rat

被引:52
作者
Lombardi, AM
Fabris, R
Bassetto, F
Serra, R
Leturque, A
Federspil, G
Girard, J
Vettor, R
机构
[1] Univ Padua, Ist Semeiot Med, Endocrine Metab Lab, Dept Med & Surg Sci, I-35100 Padua, Italy
[2] CNRS, Ctr Rech Endocrinol & Dev, F-92190 Meudon, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1999年 / 276卷 / 05期
关键词
pyruvate dehydrogenase; insulin resistance; substrate competition;
D O I
10.1152/ajpendo.1999.276.5.E922
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An increased basal plasma lactate concentration is present in many physiological and pathological conditions, including obesity and diabetes. We previously demonstrated that acute lactate infusion in rats produced a decrease in overall glucose uptake. The present study was carried out to further investigate the effect of lactate on glucose transport and utilization in skeletal muscle. In chronically catheterized rats, a 24-h sodium lactate or bicarbonate infusion was performed. To study glucose uptake in muscle, a bolus of 2-deoxy-[H-3]glucose was injected in basal condition and during euglycemic-hyperinsulinemic clamp. Our results show that hyperlactatemia decreased glucose uptake in muscles (i.e., red quadriceps; P < 0.05). Moreover in red muscles, both GLUT-4 mRNA (-30% in red quadriceps and -60% in soleus; P < 0.025) and protein (-40% in red quadriceps; P < 0.05) were decreased, whereas the (E1 alpha)pyruvate dehydrogenase (PDH) mRNA was increased (+40% in red quadriceps; P < 0.001) in lactate-infused animals. PDH protein was also increased (4-fold in red gastrocnemius and 2-fold in red quadriceps). These results indicate that chronic hyperlactatemia reduces glucose uptake by affecting the expression of genes involved in glucose metabolism in muscle, suggesting a role for lactate in the development of insulin resistance.
引用
收藏
页码:E922 / E929
页数:8
相关论文
共 52 条
[21]   DIFFERENTIAL REGULATION OF 2 GLUCOSE TRANSPORTERS IN ADIPOSE-CELLS FROM DIABETIC AND INSULIN-TREATED DIABETIC RATS [J].
KAHN, BB ;
CHARRON, MJ ;
LODISH, HF ;
CUSHMAN, SW ;
FLIER, JS .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (02) :404-411
[22]   SUPPRESSION OF GLUT4 EXPRESSION IN SKELETAL-MUSCLE OF RATS THAT ARE OBESE FROM HIGH-FAT FEEDING BUT NOT FROM HIGH-CARBOHYDRATE FEEDING OR GENETIC OBESITY [J].
KAHN, BB ;
PEDERSEN, O .
ENDOCRINOLOGY, 1993, 132 (01) :13-22
[23]  
Katzen H M, 1967, Adv Enzyme Regul, V5, P335, DOI 10.1016/0065-2571(67)90025-8
[24]   INTERACTION BETWEEN GLUCOSE AND FREE FATTY-ACID METABOLISM IN HUMAN SKELETAL-MUSCLE [J].
KELLEY, DE ;
MOKAN, M ;
SIMONEAU, JA ;
MANDARINO, LJ .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :91-98
[25]  
KRANDALL DL, 1983, HORM METAB RES, V15, P326
[26]  
KREISBERG RA, 1972, NEW ENGL J MED, V287, P132, DOI 10.1056/NEJM197207202870307
[27]   EFFECTS OF GLYCOGEN STORES AND NONESTERIFIED FATTY-ACID AVAILABILITY ON INSULIN-STIMULATED GLUCOSE-METABOLISM AND TISSUE PYRUVATE-DEHYDROGENASE ACTIVITY IN THE RAT [J].
KRUSZYNSKA, YT ;
MCCORMACK, JG ;
MCINTYRE, N .
DIABETOLOGIA, 1991, 34 (04) :205-211
[28]   Improvement of insulin action in diabetic transgenic mice selectively overexpressing GLUT4 in skeletal muscle [J].
Leturque, A ;
Loizeau, M ;
Vaulont, S ;
Salminen, M ;
Girard, J .
DIABETES, 1996, 45 (01) :23-27
[29]   NUTRITIONAL REGULATION OF GLUCOSE TRANSPORTER IN MUSCLE AND ADIPOSE-TISSUE OF WEANED RATS [J].
LETURQUE, A ;
POSTIC, C ;
FERRE, P ;
GIRARD, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (04) :E588-E593
[30]   PARALLEL INSULIN-LIKE GROWTH-FACTOR-I AND INSULIN-RESISTANCE IN MUSCLES OF RATS FED A HIGH-FAT DIET [J].
LIU, S ;
BARACOS, VE ;
QUINNEY, HA ;
LEBRICON, T ;
CLANDININ, MT .
ENDOCRINOLOGY, 1995, 136 (08) :3318-3324