2018
DOI: 10.1590/1806-9061-2018-0785
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Central Opioidergic System Interplay with Histamine on Food Intake in Neonatal Chicks: Role of µ-Opioid and H1/H3 Receptors

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Cited by 7 publications
(3 citation statements)
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References 44 publications
(55 reference statements)
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“…In this study, orofacial nociception intensity was not changed by intra-NAc microinjection of naloxone; however, it reversed the antinociceptive effect of histamine, dimaprit and thioperamide. Central opioidergic system interaction with histamine system was documented in several studies (Tamaddonfard et al ., 2011; Jaefari-Anari et al ., 2018; Salimi et al ., 2021). In this regard, an interaction was found when naloxone was applied with histamine H 2 and H 3 receptors at the cerebral cortex areas (Tamaddonfard and Hamzeh-Gooshchi, 2014; Hamzeh-Gooshchi et al ., 2015), hippocampus (Khalilzadeh et al ., 2010a; Tamaddonfard et al ., 2011), and thalamic submedius nucleus (Erfanparast et al ., 2015) in modulation of formalin-induced nociception in rats.…”
Section: Discussionmentioning
confidence: 99%
“…In this study, orofacial nociception intensity was not changed by intra-NAc microinjection of naloxone; however, it reversed the antinociceptive effect of histamine, dimaprit and thioperamide. Central opioidergic system interaction with histamine system was documented in several studies (Tamaddonfard et al ., 2011; Jaefari-Anari et al ., 2018; Salimi et al ., 2021). In this regard, an interaction was found when naloxone was applied with histamine H 2 and H 3 receptors at the cerebral cortex areas (Tamaddonfard and Hamzeh-Gooshchi, 2014; Hamzeh-Gooshchi et al ., 2015), hippocampus (Khalilzadeh et al ., 2010a; Tamaddonfard et al ., 2011), and thalamic submedius nucleus (Erfanparast et al ., 2015) in modulation of formalin-induced nociception in rats.…”
Section: Discussionmentioning
confidence: 99%
“…The µ receptor of opioid declines food consumption in chicken; however, other receptors enhance food desire (Zendehdel et al 2016). There are some interactions between opioids and other brain mediators such as 5-HT (Shojaei et al 2015), histamine (Jaefari et al 2018), NE (Nayebzadeh et al 2020), CBs (Zendehdel et al 2015c), glutamate (Torkzaban et al 2018), nitric oxide (NO) (Alimohammadi et al 2015), and OT (Raji-Dahmardeh); given this, the reduction effect of DAMGO (µ-opioid receptor agonist) is amplified by CB 1 and CB 2 receptors antagonist, H 3 receptor antagonist, and L-arginine (the precursor of NO) whereas that is diminished by NMDA and mGlu1 receptors antagonist, OT antagonist, β 2 receptor antagonist, H 1 receptors antagonist, and 5-HT 2c receptor antagonist. Also, DPDPE (δ-opioid receptors agonist) induced hyperphagia is decreased by α 1 receptor antagonist, while that is increased by AMPA glutamate receptors antagonist.…”
Section: Opioidsmentioning
confidence: 99%
“…Opioids are known as inhibitory neurotransmitters that have been connected to several acts, including pain adjustment, respiratory function, neuroendocrine and reward situation, and feeding regulation (Jaefari-Anari et al 2018). Nutrition intake was demonstrated to be changed at the time that treatments with opioid receptors agonists such as mu (µ), delta (δ), and kappa (κ) were started.…”
Section: Introductionmentioning
confidence: 99%