Previous studies in avian species have reported time-dependent losses in mu
scle glycogen with prolonged feed withdrawal (FW). However, cervical disloc
ation was used to collect tissues, a method that results in significant inv
oluntary muscle convulsions. In this study, cervical dislocation alone was
found to reduce muscle glycogen by 23%, therefore, barbiturate overdose was
used to collect tissue samples before and after FW, at the end of refeedin
g, and from continuously fed controls at each interval. Additionally, plasm
a samples from 6-wk-old male chickens were taken at the initiation and end
of a 24-hr feed withdrawal, and at various times during refeeding. After 24
hr of FW, liver glycogen decreased markedly (77%; P < 0.05), whereas muscl
e glycogen decreased slightly and transiently, such that it returned to and
remained at control levels, even after prolonged (72 hr) FW. Plasma glucos
e was decreased, whereas glucagon was elevated after a 24-hr feed withdrawa
l (P < 0.05), when compared with control concentrations. Muscle glycogen le
vels were not significantly increased over control levels after refeeding,
but liver glycogen was increased by 380% (P < 0.05). Feed deprivation follo
wed by refeeding resulted in increased circulating insulin and glucose leve
ls when compared with control levels. Therefore, by using methods of tissue
collection that ensure that muscle glycogen determinations are not confoun
ded by artifactual degradation, these results verify that regulation of avi
an muscle glycogen stores is similar to that in mammals. (C) Elsevier Scien
ce Inc. 1999.