Interaction Between Endocannabinoid and Opioidergic Systems Regulates Food Intake in Neonatal Chicken

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• 作者：Morteza Zendehdel ; Shahin Hassanpour…
• 关键词：Cannabinoidergic ; Opioidergic system ; Food intake ; Chicken
• 刊名：International Journal of Peptide Research and Therapeutics
• 出版年：2015
• 出版时间：September 2015
• 年：2015
• 卷：21
• 期：3
• 页码：289-297
• 全文大小：1,341 KB
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• 作者单位：Morteza Zendehdel (1)
  Shahin Hassanpour (2)
  Vahab Babapour (1)
  Saeed Charkhkar (2)
  Mahshid Mahdavi (3)
  
  1. Department of Physiology, Faculty of Veterinary Medicine, University of Tehran, PO Box: 14155-6453, Tehran, Iran
  2. Department of Physiology, Faculty of Veterinary Medicine, Science and Research Branch, Islamic Azad University, Tehran, Iran
  3. Department of Physiology, Faculty of Biology, Zanjan Science and Research Branch, Islamic Azad University, Zanjan, Iran
  
• 刊物类别：Biomedical and Life Sciences
• 刊物主题：Life Sciences
  Biochemistry
  Animal Anatomy, Morphology and Histology
  Polymer Sciences
  
• 出版者：Springer Netherlands
• ISSN：1573-3904

文摘

Endocannabinoids and opiates have regulatory role in some physiological functions in mammals but their interaction(s) have not been studied in avian. This survey is designed to investigate interaction of these systems on feeding behavior in neonatal chickens. In experiment 1, chicken intracerebroventricular (ICV) injected with saline, DAMGO (μ-opioid receptors agonist, 125?pmol), SR141716A (CB1 receptors antagonist, 6.25?μg) and SR141716A?+?DAMGO. In experiment 2, saline, DAMGO, AM630 (CB2 receptors antagonist, 1.25?μg) and DAMGO?+?AM630. Experiments 3- followed the procedure similar to experiments 1 and 2, except DPDPE (δ-opioid receptors agonist, 40?pmol) and U-50488H (κ-opioid receptors agonist, 30?nmol) instead of DAMGO were used. In experiment 7, saline, Naloxone (opioid receptors antagonist, 5?μg), 2-AG (CB1 receptors agonist, 2?μg), Naloxone?+?2-AG were used. Experiment 8 was similar to experiment 7, except CB65 (CB2 receptors agonist, 1.25?μg) used instead of 2-AG. Cumulative food intake was recorded until 120?min post injection. Data provided that, ICV injection of DAMGO decreased food intake and its effect amplified by CB1 and CB2 receptors antagonist (P?<?0.001). DPDPE increased food intake and CB2 receptors antagonist blocked DPDPE-induced hyperphagia (P?<?0.001). U-50488H-induced feeding but its effect did not alter via CB1 and CB2 receptors antagonist (P?>?0.05). Hyperphagia-induced by CB1 and CB2 receptors agonist amplified by naloxone (P?<?0.001). Perhaps there is interaction between endocannabinoid and opioidergic systems on appetite regulation in chicken.