Hypertension, Vol 5, 663-671, Copyright © 1983 by American Heart Association
G Feuerstein, RL Zerbe and AI Faden
This study examined the cardiovascular, respiratory, and sympathetic
effects of selective mu and delta opioid agonists microinjected into the
hypothalamic nucleus preopticus medialis (POM) of conscious SHR and WKY
rats. The mu receptor agonist D-Ala2-MePhe4-Gly5-ol-enkephalin (DAGO) at a
dose of 0.6 or 6.0 nanomoles (Nmol) increased the blood pressure and heart
rate in WKY rats. In SHR rats, the lower dose of DAGO similarly had a
pressor effect whereas the higher dose was depressor; heart rat was
increased only by the 6.0 nmol dose in these animals. In both SHR and WKY
rats, this opioid caused respiratory acidosis and elevation of plasma
norepinephrine (NE) and epinephrine (E); plasma vasopressin was reduced by
the higher dose of DAGO. All of these effects of the mu agonist were
reversed by the opiate receptor antagonist naloxone (0.5 mg/kg, i.a.). The
delta opiate-receptor agonist D-Ala2-D-leu5-eukephalin at a dose of 6.0 or
20.0 nmol increased blood pressure and heart rate in both SHR and WKY rats
without affecting respiratory variables. Plasma NE and EPI were elevated at
the peak of the pressor period. These studies suggest that the
anteroventral hypothalamic region may be an important site in central
autonomic regulation by opioid peptides. The mu-receptor agonist was more
potent than the delta agonist in eliciting cardiovascular and respiratory
effects and associated sympatho- adrenomedullary activation.(ABSTRACT
TRUNCATED AT 250 WORDS)
ARTICLES
Opiate receptors and cardiovascular control in conscious SHR and WKY rats
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