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1 School of Biomedical Sciences, University Medical School, Queen's Medical Center, Nottingham NG7 2UH; 2 Dept. of Pharmacology, Queen Mary and Westfield College, University of London, London E1 4NS; and 3 Muscle and Exercise Physiology Group, Manchester Metropolitan University, Alsager ST7 2HL, United Kingdom
Prolonged treatment with the
2-adrenoceptor agonist clenbuterol (1-2
mg · kg body mass
1 · day
1)
is known to induce the hypertrophy of fast-contracting fibers and the
conversion of slow- to fast-contracting fibers. We investigated the effects of administering a lower dose of clenbuterol (250 µg · kg body mass
1 · day
1) on skeletal muscle myosin heavy chain (MyHC)
protein isoform content and adenine nucleotide (ATP, ADP, and AMP)
concentrations. Male Wistar rats were administered clenbuterol
(n = 8) or saline (n = 6)
subcutaneously for 8 wk, after which the extensor digitorum longus
(EDL) and soleus muscles were removed. We demonstrated an increase of
type IIa MyHC protein content in the soleus from ~0.5% in controls
to ~18% after clenbuterol treatment (P < 0.05), which was accompanied by an increase in the total adenine nucleotide pool (TAN; ~19%, P < 0.05) and energy charge
[E-C = (ATP + 0.5 ADP)/(ATP + ADP + AMP); ~4%;
P < 0.05]. In the EDL, a reduction in the content of
the less prevalent type I MyHC protein from ~3% in controls to 0%
after clenbuterol treatment (P < 0.05) occurred without any alterations in TAN and E-C. These findings demonstrate that
the phenotypic changes previously observed in slow muscle after
clenbuterol administration at 1-2 mg · kg body
mass
1 · day
1 are also observed at a
substantially lower dose and are paralleled by concomitant changes in
cellular energy metabolism.
2-adrenoceptor agonist; adenosine 5'-triphosphate; energy charge; myosin heavy chain protein composition
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