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1 Department of Physiology, Faculty of Medicine of Ribeirao Preto, 2 Department of Morphology, Estomatology and Physiology, Dental School of Ribeirao Preto, University of Sao Paulo, 14040-904 Ribeirao Preto, Sao Paulo, Brazil
Hypoxia evokes
a regulated decrease in body temperature, a response that has been
termed anapyrexia, but the mechanisms involved are poorly understood.
Therefore, the present study was undertaken to test the hypothesis that
hypoxia-induced anapyrexia results from the activation of cAMP- and
cGMP-dependent pathways in the preoptic region (PO). Adult male Wistar
rats weighing 230-260 g were used. Body temperature was monitored
by biotelemetry, and the levels of cAMP and cGMP were determined in the
anteroventral third ventricular region (AV3V), where the PO is located.
Using immunohistochemistry, we observed that the PO contains a high density of cAMP- and cGMP-containing cells. Interestingly, hypoxia exposure raised the levels of cAMP and cGMP in the AV3V. Intra-PO microinjection of Rp-cAMPS, an inhibitor of cAMP-dependent protein kinase, attenuated hypoxia-induced anapyrexia. Similarly, intra-PO microinjection of the mixed
-adrenoceptor/serotonin
(5-HT1A) receptor antagonist propranolol also impaired the
drop in body temperature in response to hypoxia. The reduction in body
temperature evoked by intra-PO serotonin, but not epinephrine, was
blocked by Rp-cAMPS, indicating the involvement of a preoptic
serotonin-cAMP pathway in the development of anapyrexia. Moreover,
microinjection of
NG-monomethyl-L-arginine,
an inhibitor of nitric oxide (NO) synthesis, or Rp-cGMPS, an inhibitor
of cGMP-dependent protein kinase, into the PO also attenuated
hypoxia-induced anapyrexia. In conclusion, the present study supports
that hypoxia-induced anapyrexia results from the activation of the
serotonin-cAMP and NO-cGMP pathways in the PO.
preoptic region; hypothermia; body temperature; adenosine 3',5'-cyclic monophosphate; guanosine 3',5'-cyclic monophosphate; serotonin; nitric oxide
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