<?xml version="1.0" encoding="UTF-8"?>
<b:Sources SelectedStyle="" xmlns:b="http://schemas.openxmlformats.org/officeDocument/2006/bibliography"  xmlns="http://schemas.openxmlformats.org/officeDocument/2006/bibliography" >
<b:Source>
<b:Tag>cjs-201509-0003</b:Tag>
<b:SourceType>ArticleInAPeriodical</b:SourceType>
<b:Year>2015</b:Year>
<b:PeriodicalName>Czech Journal of Animal Science</b:PeriodicalName>
<b:Volume>60</b:Volume>
<b:Issue>9</b:Issue>
<b:Pages>400-410</b:Pages>
<b:Author>
<b:Author><b:NameList>
<b:Person><b:Last>Shojaei</b:Last><b:First>M.</b:First></b:Person>
<b:Person><b:Last>Zendehdel</b:Last><b:First>M.</b:First></b:Person>
<b:Person><b:Last>Babapour</b:Last><b:First>V.</b:First></b:Person>
<b:Person><b:Last>Charkhkar</b:Last><b:First>S.</b:First></b:Person>
<b:Person><b:Last>Hassanpour</b:Last><b:First>S.</b:First></b:Person>
</b:NameList></b:Author>
</b:Author>
<b:Title>Opioid-induced hypophagia is mediated by 5-HT&lt;sub&gt;2&lt;/sub&gt;c receptors in neonatal layer-type chicken</b:Title>
<b:Comments>Opioidergic and serotonergic (5-HTergic) systems have crucial role in central regulation of food intake. This study was designed to investigate the role of the opioidergic system and the interaction with the 5-HTergic system in opioid-induced feeding behaviour in 3-h food-deprived (FD&lt;sub&gt;3&lt;/sub&gt;) neonatal layer-type chicks. In total 432 chickens were allocated into 9 experiments, each per 4 treatment groups. In Experiment 1, birds were intracerebroventricularly (ICV) injected with D-Ala2-NMe-Phe4-Glyol5-enkephalin (DAMGO), &#181;-opioid receptor agonist (125, 250, and 500 pmol). In Experiment 2, chickens were ICV treated with D-Pen&lt;sup&gt;2&lt;/sup&gt;, D-Pen&lt;sup&gt;5&lt;/sup&gt;enkephalin (D-Pen&lt;sup&gt;2,5&lt;/sup&gt;enkephalin, DPDPE), &#948;-opioid receptor agonist (20, 40, and 80 pmol). In Experiment 3, the effect of ICV injection of U-50488H, &#954;-opioid receptor agonist (10, 20, and 30 nmol) was investigated in chicks. In Experiment 4, chickens were injected with para-chlorophenylalanine (PCPA), cerebral serotonin depletive (1.5 &#181;g) + DAMGO (125 pmol). In Experiment 5, birds were treated with PCPA (1.5 &#181;g) + DPDPE (40 pmol). In Experiment 6, birds received 1.5 &#181;g PCPA + U-50488H (30 nmol). In Experiments 7-9, birds were injected like in Experiments 4-6, but with SB242084, 5-HT&lt;sub&gt;2&lt;/sub&gt;c receptor antagonist (1.5 &#181;g) instead of the PCPA injection. Cumulative food intake was recorded until 3 h post injection. According to the results, the ICV injection of DAMGO significantly decreased whereas that of DPDPE + U-50488H increased food intake (P &#8804; 0.05). Co-administration of PCPA + DAMGO significantly decreased hypophagia induced by DAMGO (P &#8804; 0.05). PCPA had no effect on DPDPE + U-50488H-induced hyperphagia (P &#8805; 0.05). SB242084 significantly attenuated the hypophagic effect of DAMGO (P &#8804; 0.05), while SB242084 had no modulatory effect on the food intake induced by DPDPE + U-50488H (P &#8805; 0.05). These results suggest that there is an interaction between the opioidergic and 5-HTergic systems mediating the hypophagic effect of &#181;-opioid receptors via the 5-HT&lt;sub&gt;2&lt;/sub&gt;c receptor in neonatal layer-type chicks.</b:Comments>
</b:Source>
</b:Sources>
