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Journal ArticleDOI

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

TLDR
The data suggest that both mu- and kappa-opiate receptors are involved in the stimulation of ACTH release in rats, and the role of different opiate receptors in the control ofACTH release is elucidated.
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 ug/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.

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Citations
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Journal ArticleDOI

Opioid-receptor mRNA expression in the rat CNS: anatomical and functional implications

TL;DR: A broad anatomical maps of the three opioid-receptor mRNAs in relation to their binding sites is provided, and issues of receptor transport, trafficking and pre- versus postsynaptic localization are discussed.
Journal ArticleDOI

Mu, Delta, and Kappa Opioid Receptor mRNA Expression in the Rat CNS: An In Situ Hybridization Study

TL;DR: The μ, δ, and κ opioid receptors are the three main types of opioid receptors round in the central nervous system (CNS) and periphery and are important in a number of physiological functions, including analgesia, respiration, and hormonal regulation.
Journal ArticleDOI

Regulation of the hypothalamic corticotropin-releasing hormone neurosecretory system

TL;DR: The hypothalamo-pituitary-adrenal axis (HPA) and the effects of corticotropin-releasing hormone (CRH) and vasopressin (VP) on anterior pituitary cells and factors regulating CRH neurosecrctory cell activity are studied.
Journal ArticleDOI

Dynorphin, stress, and depression

TL;DR: This review summarizes current data on how KOR systems contribute to the acute, delayed, and cumulative molecular and behavioral effects of stress and focuses on behavioral paradigms that provide insight on interactions between stress and KOR function within each of these temporal categories.
Journal ArticleDOI

Immunohistochemical localization of the cloned μ opioid receptor in the rat CNS

TL;DR: Polyclonal antibodies were generated to the C terminal 63 amino acids of the cloned mu receptor to examine the distribution of the mu receptor-like protein with immunohistochemical techniques, and the anatomical and functional implications of these findings are discussed.
References
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Journal Article

Pharmacology of opioids.

W R Martin
TL;DR: There is considerable variability between species in both the specificity and selectivity of opioid receptors, and better characterization of the pharmacological profiles and receptor binding specificity for different species may help resolve some of the apparent disparities.
Journal ArticleDOI

The binding spectrum of narcotic analgesic drugs with different agonist and antagonist properties

TL;DR: Since each of the four groups of compounds, whether pure agonists, agonist-antagonists, ketazocine-like drugs or pure antagonists, shows independent varittions in the affinities to the μ- and ϰ-binding sites, their different pharmacological behaviour cannot be solely due to difference in the binding spectra.
Journal ArticleDOI

Differentiation of delta and mu opiate receptor localizations by light microscopic autoradiography

TL;DR: It is proposed that mu and delta receptors are respectively the physiologic receptors for [Met]- and [Leu]enkephalin neurons.
Journal ArticleDOI

A classification of opiate receptors that mediate antinociception in animals.

TL;DR: It is concluded that both μ‐ and κ‐opiate receptors mediate antinociception in animals and that the interactions of analgesic drugs with these receptors may be classified in terms of their antinOCiceptive activities against qualitatively different nociceptive stimuli.
Journal Article

Pharmacological characterization in vivo of the novel opiate, beta-funaltrexamine.

TL;DR: The selective long-lasting antagonism of mu-mediated effects by beta-FNA may be of great value in the elucidation of multiple opioid receptor function.
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