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Vol. 281, Issue 2, 648-654, 1997
Department of Biological Research, Boehringer Ingelheim KG, D-55216
Ingelheim am Rhein, Federal Republic of Germany
In this study, the ability of the nonselective adenosine receptor
antagonist caffeine to influence the concentration of noradrenaline in
the central nervous system was investigated, and its effects compared
with those of alpha-2 adrenoceptor modulation. The
technique of microdialysis in association with microbore
high-performance liquid chromatography and electrochemical detection
was used to measure the extracellular concentrations of noradrenaline
in the hippocampus of awake, freely moving rats. Neither the oral
administration of caffeine nor its local perfusion influenced the
base-line hippocampal levels of noradrenaline. Furthermore, the levels
of noradrenaline were not influenced by local perfusion of the
selective adenosine A1 agonist
N6-cyclopentyladenosine or by the selective adenosine
A2 agonist CGS 21680. In contrast, the extracellular levels
of noradrenaline could be increased by the perfusion of the selective
alpha-2 adrenoceptor antagonist idazoxan and decreased
by local perfusion of Ca++-free phosphate buffered saline,
a Na+-channel blocker, tetrodotoxin, or the selective
2-adrenoceptor agonist clonidine. The extracellular
levels of noradrenaline were stimulated by the local perfusion of
different concentrations of K+ (10-100 mmol/l). The
K+-dependent increase in the extracellular levels of
noradrenaline was potentiated by local perfusion of idazoxan and
inhibited by local perfusion of clonidine. In contrast, neither the
oral administration of caffeine nor its local perfusion influenced the
K+-stimulated increases in hippocampal noradrenaline.
Furthermore, local perfusion of N6-cyclopentyladenosine or
CGS 21680 did not influence the K+-stimulated levels of
noradrenaline either. These results indicate that base-line and
K+-stimulated extracellular levels of noradrenaline in the
hippocampus of awake, freely moving rats are regulated by
alpha-2 adrenoceptors and not by adenosine receptors.
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