Effects of chronic AICAR administration on the metabolic and contractile phenotypes of rat slow- and fast-twitch skeletal muscles

被引:22
作者
Bamford, JA
Lopaschuk, GD
MacLean, IM
Reinhart, ML
Dixon, WT
Putman, CT [1 ]
机构
[1] Univ Alberta, Fac Phys Educ & Recreat, Edmonton, AB T6G 2H9, Canada
[2] Univ Alberta, Ctr Neurosci, Fac Med & Dent, Van Vliet Ctr E417, Edmonton, AB T6G 2H9, Canada
[3] Univ Alberta, Heritage Med Res Ctr, Dept Paediat, Fac Med & Dent, Edmonton, AB T6G 2S2, Canada
[4] Univ Alberta, Heritage Med Res Ctr, Dept Pharmacol, Fac Med & Dent, Edmonton, AB T6G 2S2, Canada
[5] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB T6G 2S2, Canada
关键词
AMP-activated protein kinase; myosin heavy chain; metabolism; RT-PCR; SDS-PAGE;
D O I
10.1139/Y03-110
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study examined the effects of chronic activation of 5'-AMP-activated protein kinase (AMPK) on the oxidative capacity and myosin heavy chain (MHC) based fibre phenotype of rodent fast- and slow-twitch muscles. Sprague-Dawley rats received daily injections for 4 weeks of the known AMPK activator 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR) or vehicle (control). The AICAR group displayed increases in hexokinase-II (HXK-II) activity, expression, and phosphorylation in fast-twitch muscles (P < 0.001) but not in the slow-twitch soleus (SOL). In the AICAR group, citrate synthase (EC 4.1.3.7) and 3-hydroxyacyl-CoA-dehydrogenase (EC 1.1.1.35) were elevated 1.6- and 2.1-fold (P < 0.05), respectively, in fast-twitch medial gastrocnemius (MG), and by 1.2- and 1.4-fold (P < 0.05) in the slower-twitch plantaris (PLANT). No changes were observed in the slow-twitch SOL. In contrast, the activity of glyceraldehyde phosphate dehydrogenase (EC 1.2.1.12) remained unchanged in all muscles. AICAR treatment did not alter the MHC-based fibre type composition in fast- or slow-twitch muscles, as determined by immunohistochemical and electrophoretic analytical methods or by RT-PCR. We conclude that chronic activation of AMPK mimics the metabolic changes associated with chronic exercise training (increased oxidative capacity) in the fast-twitch MG and PLANT, but does not coordinately alter MHC isoform content or mRNA expression.
引用
收藏
页码:1072 / 1082
页数:11
相关论文
共 39 条
[1]   RAPID-DETERMINATION OF CREATINE, PHOSPHOCREATINE, PURINE-BASES AND NUCLEOTIDES (ATP, ADP, AMP, GTP, GDP) IN HEART BIOPSIES BY GRADIENT ION-PAIR REVERSED-PHASE LIQUID-CHROMATOGRAPHY [J].
ALLY, A ;
PARK, G .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1992, 575 (01) :19-27
[2]   AMP-activated protein kinase suppresses protein synthesis in rat skeletal muscle through down-regulated mammalian target of rapamycin (mTOR) signaling. [J].
Bolster, DR ;
Crozier, SJ ;
Kimball, SR ;
Jefferson, LS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (27) :23977-23980
[3]   MAXIMUM SHORTENING VELOCITY AND COEXISTENCE OF MYOSIN HEAVY-CHAIN ISOFORMS IN SINGLE SKINNED FAST FIBERS OF RAT SKELETAL-MUSCLE [J].
BOTTINELLI, R ;
BETTO, R ;
SCHIAFFINO, S ;
REGGIANI, C .
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1994, 15 (04) :413-419
[4]   NPS@:: Network Protein Sequence Analysis [J].
Combet, C ;
Blanchet, C ;
Geourjon, C ;
Deléage, G .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :147-150
[5]   Energy state and myosin heavy chain isoforms in single fibres of normal and transforming rabbit muscles [J].
Conjard, A ;
Peuker, H ;
Pette, D .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1998, 436 (06) :962-969
[6]   Phosphocreatine as a marker of contractile activity in single muscle fibres [J].
Conjard, A ;
Pette, D .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1999, 438 (03) :278-282
[7]   METABOLITE PATTERNS RELATED TO EXHAUSTION, RECOVERY AND TRANSFORMATION OF CHRONICALLY STIMULATED RABBIT FAST-TWITCH MUSCLE [J].
GREEN, HJ ;
DUSTERHOFT, S ;
DUX, L ;
PETTE, D .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1992, 420 (3-4) :359-366
[8]   The effects of AICAR on adipocyte differentiation of 3T3-L1 cells [J].
Habinowski, SA ;
Witters, LA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 286 (05) :852-856
[9]  
Hardie DG, 1999, BIOCHEM SOC SYMP, P13
[10]   Stimulation of rat liver AMP-activated protein kinase by AMP analogues [J].
Henin, N ;
Vincent, MF ;
VandenBerghe, G .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1996, 1290 (02) :197-203