Training intensity-dependent and tissue-specific increases in lactate uptake and MCT-1 in heart and muscle

被引:103
作者
Baker, SK [1 ]
McCullagh, KJA [1 ]
Bonen, A [1 ]
机构
[1] Univ Waterloo, Dept Kinesiol, Waterloo, ON N2L 3G1, Canada
关键词
citrate synthase; soleus; extensor digitorum longus; red gastrocnemius; white gastrocnemius;
D O I
10.1152/jappl.1998.84.3.987
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We investigated the effects of 3 wk of moderate-(21 m/min, 8% grade) and high-intensity treadmill training (31 m/min, 15% grade) on 1) monocarboxylate transporter 1 (MCT-1) content in rat hindlimb muscles and the heart and 2) lactate uptake in isolated soleus (Sol) muscles and perfused hearts. In the moderately trained group MCT-1 was not increased in any of the muscles [Sol, extensor digitorum longus (EDL), and red (RG) and white gastrocnemius (WG)] (P > 0.05). Similarly, lactate uptake in Sol strips was also not increased (P > 0.05). In contrast, in the heart, MCT-1 (+36%, P < 0.05) and lactate uptake (+72% P < 0.05) were increased with moderate training. In the highly trained group, MCT-1 (+70%, P < 0.05) and lactate uptake (+79%, P < 0.05) were increased in Sol. MCT-1 was also increased in RG (+ 94%, P < 0.05) but not in WG and EDL (P > 0.05). In the highly trained group, heart MCT-1 (+44%, P < 0.05) and lactate uptake (+173%, P < 0.05) were increased. In conclusion, it has been shown that I) in both heart and skeletal muscle lactate uptake is increased only when MCT-1 is increased; 2) training-induced increases in MCT-1 occurred at a lower training intensity in the heart than in skeletal muscle; 3) in the heart, lactate uptake was increased much more after high-intensity training than after moderate-intensity training, despite similar increases in heart MCT-1 with these two training intensities; and 4) the increases in MCT-1 occurred independently of any changes in the heart's oxidative capacity (as measured by citrate synthase activity).
引用
收藏
页码:987 / 994
页数:8
相关论文
共 40 条
[31]   CDNA CLONING AND FUNCTIONAL-CHARACTERIZATION OF RAT INTESTINAL MONOCARBOXYLATE TRANSPORTER [J].
TAKANAGA, H ;
TAMAI, I ;
INABA, S ;
SAI, Y ;
HIGASHIDA, H ;
YAMAMOTO, H ;
TSUJI, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 217 (01) :370-377
[32]   PARTICIPATION OF A PROTON-COTRANSPORTER, MCT1, IN THE INTESTINAL TRANSPORT OF MONOCARBOXYLIC ACIDS [J].
TAMAI, I ;
TAKANAGA, H ;
OGIHARA, T ;
HIGASHIDA, H ;
MAEDA, H ;
SAI, Y ;
TSUJI, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 214 (02) :482-489
[33]  
TIIDUS PM, 1994, MED SCI SPORT EXER, V26, P354
[34]   FUNCTIONAL-CHARACTERISTICS OF THE CARDIAC SARCOLEMMAL MONOCARBOXYLATE TRANSPORTER [J].
TROSPER, TL ;
PHILIPSON, KD .
JOURNAL OF MEMBRANE BIOLOGY, 1989, 112 (01) :15-23
[35]   LACTATE TRANSPORT BY CARDIAC SARCOLEMMAL VESICLES [J].
TROSPER, TL ;
PHILIPSON, KD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (05) :C483-C489
[36]   MECHANISMS OF PH(I) RECOVERY AFTER GLOBAL-ISCHEMIA IN THE PERFUSED HEART [J].
VANDENBERG, JI ;
METCALFE, JC ;
GRACE, AA .
CIRCULATION RESEARCH, 1993, 72 (05) :993-1003
[37]   Substrate and inhibitor specificities of the monocarboxylate transporters of single rat heart cells [J].
Wang, X ;
Levi, AJ ;
Halestrap, AP .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 270 (02) :H476-H484
[38]   KINETICS OF THE SARCOLEMMAL LACTATE CARRIER IN SINGLE HEART-CELLS USING BCECF TO MEASURE PH(I) [J].
WANG, XM ;
LEVI, AJ ;
HALESTRAP, AP .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1994, 267 (05) :H1759-H1769
[39]   CHARACTERIZATION OF THE INHIBITION BY STILBENE DISULPHONATES AND PHLORETIN OF LACTATE AND PYRUVATE TRANSPORT INTO RAT AND GUINEA-PIG CARDIAC MYOCYTES SUGGESTS THE PRESENCE OF 2 KINETICALLY DISTINCT CARRIERS IN HEART-CELLS [J].
WANG, XM ;
POOLE, RC ;
HALESTRAP, AP ;
LEVI, AJ .
BIOCHEMICAL JOURNAL, 1993, 290 :249-258
[40]   L(+)-LACTATE TRANSPORT IN PERFUSED RAT SKELETAL-MUSCLE - KINETIC CHARACTERISTICS AND SENSITIVITY TO PH AND TRANSPORT INHIBITORS [J].
WATT, PW ;
MACLENNAN, PA ;
HUNDAL, HS ;
KURET, CM ;
RENNIE, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 944 (02) :213-222