1995
DOI: 10.1016/0143-4179(95)90025-x
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Opioid peptide inhibition of endogenous norepinephrine release from the A2 noradrenergic cell group in vitro

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Cited by 11 publications
(5 citation statements)
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“…• Suppression of attention to novelty via the inhibition of NE release [159, 160, 163-166] that would enhance a sense of predictability of the surroundings and of the capacity to handle it.…”
Section: The Roles Of or In Dispositions As A First Sketch Of Directionality Of Behaviour: The “?I!”-systemmentioning
confidence: 99%
See 1 more Smart Citation
“…• Suppression of attention to novelty via the inhibition of NE release [159, 160, 163-166] that would enhance a sense of predictability of the surroundings and of the capacity to handle it.…”
Section: The Roles Of or In Dispositions As A First Sketch Of Directionality Of Behaviour: The “?I!”-systemmentioning
confidence: 99%
“…Instead it is the failure of other systems that gives a way to hormonal systems to control the integration of actions, and DOR simply speeds up whatever was chosen. All 3 axes are suppressed by endorphins and enkephalins that bind to (and activate) MORs and DORs (marked here as “I!”) [93, 159, 160].…”
Section: Towards Taxonomies Of Contingencies In Neurochemical Construction Of Behaviourmentioning
confidence: 99%
“…There is good consensus in neurochemistry on the key role of endorphins binding to mu-opioid receptors (MORs) in positive emotional valence, physical and emotional pain relief (Leknes, 2008;Bodnar, 2018), relaxation, feeling of security, and affiliation (Barr et al, 2008;Curley, 2011). The action of MOR, activated by endorphins, suppresses the activation of the Hypothalamicpituitary-adrenal (HPA) axis (i.e., suppresses mobilisation for an action) and induces the release of dopamine (DA) (Werling et al, 1988;Carr and Gregg, 1995;Degli Uberti et al, 1995;Yamauchi et al, 1997;Bodnar, 2018). There are several sites in the body and the brain that manufacture endorphins, and we can classify these sites into three groups (Figure 2).…”
Section: The Roles Of Opioid Receptor Systems In Emotional Valence and Alertnessmentioning
confidence: 99%
“…The other locations of MOR in the brain, which the endorphins bind to, were linked to behavioural homeostatic maintenance (Golgi cells in the cerebellum and in reticular formation) as well as motivational and programming processes [nucleus accumbens (NAc), ventral tegmental area (VTA), prefrontal cortex (PFC), amygdala (AM), HT, PAG] (Hamel and Beaudet, 1984;Nieuwenhuys, 1985;Peckys and Landwehrmeyer, 1999;Le Merrer et al, 2009). MOR, and also delta-opioid receptors (DORs), are G protein-coupled receptors (GPCRs) regulating the release of MAs, including the facilitation of dopamine release (Werling et al, 1988;Carr and Gregg, 1995;Degli Uberti et al, 1995;Yamauchi et al, 1997;Bodnar, 2018). Considering the "approval" effect of endorphins and their links to positive emotional valence, there is no surprise that these brain structures were noted for their involvement in motivation, planning, and anticipation.…”
Section: Endorphins Are Produced By the Bone Marrow Inmentioning
confidence: 99%
“…Opioid peptides of all three classes (mu-, kappa-and delta-) are known to interact with dopaminergic systems within median eminence. A number of neural systems and estradiol (E) (Ben-Jonathan and Hnasko, 2001) are thought to be involved in opioid-mediated hormone release, including noradrenergic (Carr and Gregg, 1995), cholinergic (Kaur, 2001), GABAergic (Kaur, 2001), serotonergic (Foresta et al, 1986), and dopaminergic systems Schlussman et al, 2002).…”
Section: Prolactin Regulationmentioning
confidence: 99%