Purpose: Recently, it was shown that glycogen supercompensation tended (P =
0.06) to be greater if creatine and glycogen were loaded simultaneously. B
ecause the authors suggested that creatine loading increased cell volumes a
nd, therefore. enhanced glycogen supercompensation, we decided to determine
whether an enhanced glycogen supercompensation could be realized if the gl
ycogen loading protocol was preceded by a 5-d creatine load. Methods: Twelv
e men (19-28 yr) performed two standard glycogen loading protocols interspe
rsed with a standard creatine load of 20 g .d(-1) for 5 d. The vastus later
alis muscle was biopsied before and after each loading protocol. Results: T
he initial glycogen loading protocol showed a significant 4% increase (P <
0.05) in muscle glycogen (<Delta> up arrow 161 +/- 87 mmol . kg(-1) d.m.),
and no change (P > 0.05) in total muscle creatine. Biopsies pre- and post-c
reatine loading showed significant increases in total muscle creatine level
s in both the left leg (Delta up arrow 41.1 +/- 31.1 mmol . kg(-1) d.m.) an
d the right leg (Delta up arrow 36.6 +/- 19.8 mmol . kg(-1) d.m.), with no
change in either leg's muscle glycogen content. After the final glycogen lo
ading, a significant 53% increase in muscle glycogen (Delta up arrow 241 +/
- 150 mmol . kg(-1) d.m.) was detected. Finally, the postcreatine load tota
l glycogen content (694 +/- 156 mmol . kg(-1) d.m.) was significantly (P <
0.05) greater than the precreatine load total glycogen content (597 +/- 142
mmol . kg(-1) d.m.). Conclusion: It is suggested that a muscle's glycogen
loading capacity is influenced by its initial levels of creatine and the ac
companying alterations in cell volume.