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<mods ID="cjs-201509-0003">
	<titleInfo><title>Opioid-induced hypophagia is mediated by 5-HT&lt;sub&gt;2&lt;/sub&gt;c receptors in neonatal layer-type chicken</title></titleInfo>
	<name type="personal">
		<namePart type="family">Shojaei</namePart>
		<namePart type="given">M.</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">Zendehdel</namePart>
		<namePart type="given">M.</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">Babapour</namePart>
		<namePart type="given">V.</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">Charkhkar</namePart>
		<namePart type="given">S.</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">Hassanpour</namePart>
		<namePart type="given">S.</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<typeOfResource>text</typeOfResource>
	<genre>journal article</genre>
	<originInfo><dateIssued>2015</dateIssued></originInfo>
	<language></language>
	<abstract lang="English">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>
	<subject><topic>opioidergic; 5-HTergic system; food intake; layer-type chicks</topic></subject>
	<identifier type="doi">10.17221/8458-CJAS</identifier>
	<identifier type="uri">https://cjas.agriculturejournals.cz/artkey/cjs-201509-0003.php</identifier>
	<location><url>https://cjas.agriculturejournals.cz/artkey/cjs-201509-0003.php</url></location>
	<relatedItem type="host">
		<titleInfo><title>Czech Journal of Animal Science</title></titleInfo>
		<originInfo><issuance>continuing</issuance></originInfo>
		<part>
			<detail type="volume"><number>60</number></detail>
			<detail type="issue"><number>9</number></detail>
			<extent unit="pages">
				<start>400</start>
				<end>410</end>
			</extent>
			<date>2015</date>
		</part>
		<identifier type="issn">12121819</identifier>
		<genre authority="marc">periodical</genre>
		<genre>academic journal</genre>
	</relatedItem>
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