Mj. Smith et Rv. Gallo, FURTHER-STUDIES ON THE SUPPRESSION OF LUTEINIZING-HORMONE RELEASE DUETO ACTIVATION OF MEDIAL PREOPTIC-ANTERIOR HYPOTHALAMIC AREA MU-OPIOIDRECEPTORS, Brain research bulletin, 42(1), 1997, pp. 1-7
Our laboratory has previously demonstrated that specific activation of
mu-opioid receptors in the medial preoptic-anterior hypothalamic area
with [D-Ala(2), N Me-Phe(4), Gly-ol(5)]-enkephalin (DAGO) suppresses
luteinizing hormone secretion in the ovariectomized rat [29]. In the p
resent study, three experiments were undertaken to ascertain whether c
hanges in the activity of norepinephrine or dopamine neurons modulate
the decrease in luteinizing hormone release in response to DAGO. The f
irst experiment utilized push-pull perfusion in conjunction with HPLC
to assess in vivo norepinephrine release in the medial preoptic-anteri
or hypothalamic area in response to perfusion of this site with DAGO (
5 mu g/h). DAGO significantly decreased luteinizing hormone release, b
ut perfusate norepinephrine levels did not change. In the second exper
iment, push-pull perfusion in the medial preoptic-anterior hypothalami
c area with cerebrospinal fluid (CSF) or CSF containing DAGO was done
in rats pretreated with the norepinephrine synthesis inhibitor, FLA-63
. This drug pretreatment had no effect on the DAGO-induced suppression
of luteinizing hormone secretion. In Experiment 3, push-pull perfusio
n in the medial preoptic-anterior hypothalamic area with CSF followed
by CSF containing DAGO was done in rats pretreated with vehicle, or a
dopamine receptor antagonist, either pimozide or d-butaclamol. Neither
dopamine receptor antagonist had any effect on the DAGO-induced suppr
ession of luteinizing hormone release. Thus, these studies do not supp
ort a role for alterations in the activity of norepinephrine or dopami
ne neurons in mediating the suppression of luteinizing hormone release
in response to activation of mu-opioid receptors in the medial preopt
ic-anterior hypothalamic area in the ovariectomized rat. Copyright (C)
1997 Elsevier Science Inc.