Central kappa- and mu-opiate receptors mediate ACTH-release in rats.

Abstract:

:The control of ACTH secretion by opiates seems to involve stimulatory and inhibitory pathways, since opiate agonists and antagonists are capable of releasing ACTH in conscious rats. To elucidate the role of different opiate receptors in the control of ACTH release, rats were treated with receptor-selective opiate agonists and antagonists. The mu-opiate agonists, morphine and (D-Ala2, MePhe4, Gly5-ol)enkephalin, and the benzomorphan kappa-opiate agonists, MR 2034 and MRZ 2549, both stimulated ACTH release after central or peripheral injection. The effects of morphine, but not those of MR 2034, were blocked by a low dose of naloxone (50 micrograms/kg) and by the mu-receptor antagonist, beta-funaltrexamine. A 20 times higher dose of naloxone also blocked the effects of the kappa-agonist. Our data suggest that both mu- and kappa-opiate receptors are involved in the stimulation of ACTH release in rats.

journal_name

Endocrinology

journal_title

Endocrinology

authors

Pfeiffer A,Herz A,Loriaux DL,Pfeiffer DG

doi

10.1210/endo-116-6-2688

subject

Has Abstract

pub_date

1985-06-01 00:00:00

pages

2688-90

issue

6

eissn

0013-7227

issn

1945-7170

journal_volume

116

pub_type

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