Je. Schneider et al., CENTRAL VS PERIPHERAL METABOLIC CONTROL OF ESTROUS CYCLES IN SYRIAN-HAMSTERS .2. GLUCOPRIVATION, American journal of physiology. Regulatory, integrative and comparative physiology, 41(1), 1997, pp. 406-412
Estrous cycles in Syrian hamsters are inhibited by food deprivation or
treatment with pharmacological inhibitors of intracellular glucose ut
ilization (glucoprivic treatments). These same metabolic challenges in
crease neural stimulation in areas of the caudal brain stem thought to
be involved in detection of metabolic signals. Experiment 1 was desig
ned to examine whether vagally transmitted signals are important for g
lucoprivic effects on estrous cycles and on neural stimulation in the
caudal brain stem. Vagotomized or sham-operated hamsters were treated
with 2-deoxy-D-glucose (2-DG) at a dose known to decrease cellular glu
cose utilization and inhibit estrous cycles (1,750 mg/kg). Vagotomized
and sham-operated hamsters did not differ significantly in incidence
of 2-DG-induced anestrus or in neural stimulation in the caudal brain
stem, but the effects of 2-DG on estrous cycles and neural stimulation
appeared to have been attenuated in vagotomized hamsters. In experime
nt 2, hamsters were injected intracerebroventricularly with 2-DG or gl
ucose at doses that did not induce anestrus when injected systemically
(125 and 250 mg/kg). Groups treated with intracerebroventricular inje
ctions of 2-DG showed a significantly higher incidence of anestrus tha
n those treated with glucose. In experiment 3, effects of systemic inj
ections of 2-DG were prevented by prior injection of glucose on fructo
se at the same concentration, indicating that 2-DG acts via effects on
glucose metabolism, rather than via a nonspecific pharmacological eff
ect or generalized stress response. Results of these experiments and t
hose reported elsewhere [J. E. Schneider, A. J. Hall, and G. N. Wade.
Am. J. Physiol. 272 (Regulatory Integrative Comp. Physiol. 41): R400-R
405, 1997] are consistent with the notion that central glucoprivation
is sufficient, whereas peripheral lipoprivation is not critical, for m
etabolic effects on estrous cycles.