CHANGES IN PLASMA-FREE FATTY-ACIDS AND GLYCEROLS DURING PROLONGED EXERCISE IN TRAINED AND HYPERTENSIVE PERSONS TAKING PROPRANOLOL AND PINDOLOL

被引:12
作者
JESEK, JK [1 ]
MARTIN, NB [1 ]
BROEDER, CE [1 ]
THOMAS, EL [1 ]
WAMBSGANS, KC [1 ]
HOFMAN, Z [1 ]
IVY, JL [1 ]
WILMORE, JH [1 ]
机构
[1] UNIV TEXAS,DEPT KINESIOL & HLTH EDUC,HUMAN PERFORMANCE LAB,BELLMONT HALL 222,AUSTIN,TX 78712
关键词
D O I
10.1016/0002-9149(90)91164-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The extent to which lipolysis is attenuated during prolonged submaximal exercise during β blockade was determined in 12 normotensive endurance-trained and 12 hypertensive sedentary men using nonselective drugs with and without intrinsic sympathomimetic activity (ISA). Initially, subjects performed a graded treadmill test to determine maximal oxygen uptake (V̇O2max). This was followed by 2-hour walks at 25 and 45% of the subject's V̇O2max under each of 3 treatments: pindolol (ISA), propranolol (non-ISA) and placebo. The distribution of medication was randomized and double blinded. Blood samples taken at rest and every 30 minutes during the 2-hour walks were analyzed to determine the concentrations of free fatty acids (FFA) and glycerol. On the basis of the respective changes in FFA, glycerols and the respiratory exchange ratio, β-adrenergic blockade did not attenuate lipolysis in the untrained hypertensive subjects when compared with the placebo administration. However, β blockade did demonstrate a tendency to attenuate lipolysis in the trained, normotensive subjects when compared with results after placebo administration. This was particularly evident at 30 minutes of exercise, when both glycerol and FFA concentrations were not increased above resting values under both conditions of β blockade. No differences between pindolol and propranolol were observed. Therefore, a β-blocking agent with ISA properties appears to have no clear benefit with respect to lipid metabolism during low and moderate intensity exercise. Furthermore, these data demonstrate that β blockade does not inhibit exercise-induced lipolysis at low and moderate intensities of exercise as formerly believed, and is unlikely to be the cause of fatigue normally observed during work in patient populations taking β-blocking medication. © 1990.
引用
收藏
页码:1336 / 1341
页数:6
相关论文
共 25 条
[1]   CONCENTRATION OF TRIGLYCERIDES, PHOSPHOLIPIDS AND GLYCOGEN IN SKELETAL MUSCLE AND OF FREE FATTY ACIDS AND BETA-HYDROXYBUTYRIC ACID IN BLOOD IN MAN IN RESPONSE TO EXCERCISE [J].
CARLSON, LA ;
EKELUND, LG ;
FROBERG, SO .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1971, 1 (04) :248-&
[2]   EFFECTS OF BETA-1-BETA-2-BLOCKADE VS BETA-1+BETA-2-BLOCKADE ON EXERCISE ENDURANCE AND MUSCLE METABOLISM IN HUMANS [J].
CLEROUX, J ;
VANNGUYEN, P ;
TAYLOR, AW ;
LEENEN, FHH .
JOURNAL OF APPLIED PHYSIOLOGY, 1989, 66 (02) :548-554
[3]   COLORIMETRIC MICRO-DETERMINATION OF NON-ESTERIFIED FATTY ACIDS IN PLASMA [J].
DUNCOMBE, WG .
CLINICA CHIMICA ACTA, 1964, 9 (02) :122-&
[4]   ASPECTS OF HORMONAL-REGULATION OF LIPOLYSIS DURING EXERCISE - EFFECTS OF CHRONIC BETA-RECEPTOR BLOCKADE [J].
FRANZ, IW ;
LOHMANN, FW ;
KOCH, G ;
QUABBE, HJ .
INTERNATIONAL JOURNAL OF SPORTS MEDICINE, 1983, 4 (01) :14-20
[5]   DIFFERENCE BETWEEN BETA-1-SELECTIVE AND NON-SELECTIVE BETA-BLOCKADE DURING CONTINUOUS AND INTERMITTENT EXERCISE [J].
GULLESTAD, L ;
DOLVA, LO ;
SOYLAND, E ;
KJEKSHUS, J .
CLINICAL PHYSIOLOGY, 1988, 8 (05) :487-499
[6]   THE INFLUENCE OF BETA-ADRENOCEPTOR BLOCKADE ON THE LIPOLYTIC RESPONSE TO EXERCISE [J].
HALL, PE ;
SMITH, SR ;
JACK, DB ;
KENDALL, MJ .
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS, 1987, 12 (02) :101-106
[7]  
HESPEL P, 1986, MED SCI SPORT EXER, V18, P186
[8]  
Holloszy J O, 1977, Ann N Y Acad Sci, V301, P440, DOI 10.1111/j.1749-6632.1977.tb38220.x
[9]  
JUHLINDANNFELT A, 1982, ACTA MED SCAND S, V665, P113
[10]   EFFECTS OF SHORT-TERM AND LONG-TERM TREATMENT WITH CARDIOSELECTIVE AND NON-SELECTIVE BETA-RECEPTOR BLOCKADE ON CARBOHYDRATE AND LIPID-METABOLISM AND ON PLASMA-CATECHOLAMINES AT REST AND DURING EXERCISE [J].
KOCH, G ;
FRANZ, IW ;
LOHMANN, FW .
CLINICAL SCIENCE, 1981, 61 :S433-S435