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	<source-app name="Actavia">Actavia</source-app>
	<ref-type name="Journal Article">0</ref-type>
	<contributors>
		<authors>
			<author>Shojaei, M.</author>
			<author>Zendehdel, M.</author>
			<author>Babapour, V.</author>
			<author>Charkhkar, S.</author>
			<author>Hassanpour, S.</author>
		</authors>
		<secondary-authors></secondary-authors>
	</contributors>
	<titles><title>Opioid-induced hypophagia is mediated by 5-HT&lt;sub&gt;2&lt;/sub&gt;c receptors in neonatal layer-type chicken</title></titles>
	<dates>
		<year>2015</year>
		<pub-dates><date>2015-9-30</date></pub-dates>
	</dates>
	<pages>400-410</pages>
	<abstract>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), µ-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), δ-opioid receptor agonist (20, 40, and 80 pmol). In Experiment 3, the effect of ICV injection of U-50488H, κ-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 µg) + DAMGO (125 pmol). In Experiment 5, birds were treated with PCPA (1.5 µg) + DPDPE (40 pmol). In Experiment 6, birds received 1.5 µg 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 µg) 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 ≤ 0.05). Co-administration of PCPA + DAMGO significantly decreased hypophagia induced by DAMGO (P ≤ 0.05). PCPA had no effect on DPDPE + U-50488H-induced hyperphagia (P ≥ 0.05). SB242084 significantly attenuated the hypophagic effect of DAMGO (P ≤ 0.05), while SB242084 had no modulatory effect on the food intake induced by DPDPE + U-50488H (P ≥ 0.05). These results suggest that there is an interaction between the opioidergic and 5-HTergic systems mediating the hypophagic effect of µ-opioid receptors via the 5-HT&lt;sub&gt;2&lt;/sub&gt;c receptor in neonatal layer-type chicks.</abstract>
	<number>9</number>
	<volume>60</volume>
</record>
</records>
</xml>
