Regulation of glucose kinetics during intense exercise in humans:: Effects of α- and β-adrenergic blockade

被引:10
作者
Howlett, KF [1 ]
Watt, MJ
Hargreaves, M
Febbraio, MA
机构
[1] Deakin Univ, Sch Hlth Sci, Exercise Muscle & Metab Unit, Burwood, Vic 3125, Australia
[2] RMIT Unit, Skeletal Muscle Res Lab, Sch Med Sci, Bundoora, Vic, Australia
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2003年 / 52卷 / 12期
基金
澳大利亚研究理事会;
关键词
D O I
10.1016/S0026-0495(03)00330-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study examined the effect of combined alpha- and beta-adrenergic blockade on glucose kinetics during intense exercise. Six endurance-trained men exercised for 20 minutes at approximately 78% of their peak oxygen consumption (VO2) following ingestion of a placebo (CON) or combined a- (prazosin hydrochloride) and beta- (timolol maleate) adrenoceptor antagonists (BLK). Plasma glucose increased during exercise in CON (0 minutes: 5.5 +/- 0.1; 20 minutes: 6.5 0.3 mmol - L-1, P < .05). In BLK, the exercise-induced increase in plasma glucose was abolished (0 minutes: 5.7 +/- 0.3; 20 minutes: 5.7 +/- 0.1 mmol . L-1). Glucose kinetics were measured using a primed, continuous infusion of [6,6-H-2] glucose. Glucose production wwas not different between trials; on average these values were 25.3 +/- 3.9 and 30.9 +/- 4.4 mumol . kg(-1) - min(-1) in CON and BLK, respectively. Glucose uptake during exercise was greater (P < .05) in BLK (30.6 +/- 4.6 mumol . kg(-1) . min(-1)) compared with CON (18.4 +/- 2.5 mumol . kg(-1) . min(-1)). In BLIK, plasma insulin and catecholamines were higher (P < .05), while plasma glucagon was unchanged from CON. Free fatty acids (FFA) and glycerol were lower (P < .05) in BLK. These findings demonstrate that adrenergic blockade during intense exercise results in a blunted plasma glucose response that is due to enhanced glucose uptake, with no significant change in glucose production. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1615 / 1620
页数:6
相关论文
共 33 条
[1]   GLUCAGON LEVELS IN NORMAL AND DIABETIC SUBJECTS - USE OF A SPECIFIC IMMUNOABSORBENT FOR GLUCAGON RADIOIMMUNOASSAY [J].
ALFORD, FP ;
BLOOM, SR ;
NABARRO, JDN .
DIABETOLOGIA, 1977, 13 (01) :1-6
[2]   ADRENERGIC REGULATION OF LIPOLYSIS INSITU AT REST AND DURING EXERCISE [J].
ARNER, P ;
KRIEGHOLM, E ;
ENGFELDT, P ;
BOLINDER, J .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (03) :893-898
[3]   SENSITIVITY OF EXERCISE-INDUCED INCREASE IN HEPATIC GLUCOSE-PRODUCTION TO GLUCOSE SUPPLY-AND-DEMAND [J].
BERGER, CM ;
SHARIS, PJ ;
BRACY, DP ;
LACY, DB ;
WASSERMAN, DH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (03) :E411-E421
[4]   Splanchnic blood flow and hepatic glucose production in exercising humans:: role of renin-angiotensin system [J].
Bergeron, R ;
Kjær, M ;
Simonsen, L ;
Bülow, J ;
Skovgaard, D ;
Howlett, K ;
Galbo, H .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2001, 281 (06) :R1854-R1861
[5]   RELEASE AND CLEARANCE RATES OF EPINEPHRINE IN MAN - IMPORTANCE OF ARTERIAL MEASUREMENTS [J].
BEST, JD ;
HALTER, JB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1982, 55 (02) :263-268
[6]   EPINEPHRINE ADMINISTRATION STIMULATES GLUT4 TRANSLOCATION BUT REDUCES GLUCOSE-TRANSPORT IN MUSCLE [J].
BONEN, A ;
MEGENEY, LA ;
MCCARTHY, SC ;
MCDERMOTT, JC ;
TAN, MH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 187 (02) :685-691
[7]  
Chernick S, 1969, METH ENZYMOLOGY, V14, P627
[8]   SLEEP-ASSOCIATED FALL IN GLUCOSE DISPOSAL AND HEPATIC GLUCOSE OUTPUT IN NORMAL HUMANS - PUTATIVE SIGNALING MECHANISM LINKING PERIPHERAL AND HEPATIC EVENTS [J].
CLORE, JN ;
NESTLER, JE ;
BLACKARD, WG .
DIABETES, 1989, 38 (03) :285-290
[9]   Regulation of glucose production during exercise at 80% of VO2peak in untrained humans [J].
Coggan, AR ;
Raguso, CA ;
Gastaldelli, A ;
Williams, BD ;
Wolfe, RR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (02) :E348-E354
[10]   Role of hepatic alpha- and beta-adrenergic receptor stimulation on hepatic glucose production during heavy exercise [J].
Coker, RH ;
Krishna, MG ;
Lacy, DB ;
Bracy, DP ;
Wasserman, DH .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (05) :E831-E838