Endocannabinoid and nitric oxide interaction mediates food intake in neonatal chicken

REFERENCES

• Alimohammadi, S., Zendehdel, M. & Babapour, V. (2015) Modulation of opioid-induced feeding behavior by endogenous nitric oxide in neonatal layer-type chicks. Veterinary Research Communications, 39: 105–113. doi:10.1007/s11259-015-9631-8
   PubMed Web of Science ®Google Scholar
• Azad, S.C., Marsicano, G., Eberlein, I., Putzke, J., Zieglgaènsberger, W., Spanagel, R. & Lutz, B. (2001) Differential role of the nitric oxide pathway on ∆9-THC-induced central nervous system effects in the mouse. European Journal of Neuroscience, 13: 561–568. doi:10.1046/j.1460-9568.2001.01431.x
   PubMed Web of Science ®Google Scholar
• Chen, R.Z., Frassetto, A. & Fong, T.M. (2006) Effects of the CB1 cannabinoid receptor inverse agonist AM251 on food intake and body weight in mice lacking μ-opioid receptors. Brain Research, 1108: 176–178. doi:10.1016/j.brainres.2006.06.006
   PubMed Web of Science ®Google Scholar
• Choi, Y.H., Furuse, M., Okumura, J. & Denbow, D.M. (1995) The interaction of clonidine and nitric oxide on feeding behavior in the chicken. Brain Research, 699: 161–164. doi:10.1016/0006-8993(95)01057-3
   PubMed Web of Science ®Google Scholar
• Díaz-Arteaga, A., Vázquez, M.J., Vazquez-Martínez, R., Pulido, M.R., Suarez, J., Velásquez, D.A., López, M., Ross, R.A., Rodriguez de Fonseca, F., Bermudez-Silva, F.J., Malagón, M.M., Diéguez, C. & Nogueiras, R. (2012) The atypical cannabinoid O-1602 stimulates food intake and adiposity in rats. Diabetes Obesity and Metabolism, 14: 234–243. doi:10.1111/j.1463-1326.2011.01515.x
   PubMed Web of Science ®Google Scholar
• D’addario, C., Micioni Di Bonaventura, M.V., Pucci, M., Romano, A., Gaetani, S., Ciccocioppo, R., Cifani, C. & Maccarrone, M. (2014) Endocannabinoid signaling and food addiction. Neuroscience & Biobehavioral Reviews, 47: 203–224. doi:10.1016/j.neubiorev.2014.08.008
   PubMed Web of Science ®Google Scholar
• Davis, J.L., Masuoka, D.T., Gerbrandt, L.K. & Cherkin, A. (1979) Autoradiographic distribution of l-proline in chicks after intracerebral injection. Physiology & Behavior, 22: 693–695. doi:10.1016/0031-9384(79)90233-6
   PubMed Web of Science ®Google Scholar
• De Luca, B., Monda, M. & Sullo, A. (1995) Changes in eating behavior and thermogenic activity following inhibition of nitric oxide formation. American Journal of Physiology, 268: R1533–R1538.
   PubMed Web of Science ®Google Scholar
• Denbow, D.M. (1994) Peripheral regulation of food intake in poultry. Journal of Nutrition, 124: 1349S–1354S.
   PubMed Web of Science ®Google Scholar
• Emadi, L., Jonaidi, H. & Hosseini Amir Abad, E. (2011) The role of central CB2 cannabinoid receptors on food intake in neonatal chicks. Journal of Comparative Physiology A, 197: 1143–1147. doi:10.1007/s00359-011-0676-z
   Web of Science ®Google Scholar
• Fattore, L., Fadda, P., Spano, M.S., Pistis, M. & Fratta, W. (2008) Neurobiological mechanisms of cannabinoid addiction. Molecular and Cellular Endocrinology, 286: S97–S107. doi:10.1016/j.mce.2008.02.006
   PubMed Web of Science ®Google Scholar
• Fowler, C.J., Nilsson, O., Andersson, M., Disney, G., Jacobsson, S.O. & Tiger, G. (2001) Pharmacological properties of cannabinoid receptors in the avian brain: similarity of rat and chicken cannabinoid1 receptor recognition sites and expression of cannabinoid2 receptor-like immunoreactivity in the embryonic chick brain. Pharmacology and Toxicology, 88: 213–222. doi:10.1034/j.1600-0773.2001.d01-107.x
   PubMedGoogle Scholar
• Furuse, M., Matsumoto, M., Saito, N., Sugahara, K. & Hasegawa, S. (1997) The central corticotropin-releasing factor and glucagon-like peptide-1 in food intake of the neonatal chick. European Journal of Pharmacology, 339: 211–213. doi:10.1016/S0014-2999(97)01391-5
   PubMed Web of Science ®Google Scholar
• Jonaidi, H. & Noori, Z. (2012) Neuropeptide Y-induced feeding is dependent on GABAA receptors in neonatal chicks. Journal of Comparative Physiology A, 198: 827–832. doi:10.1007/s00359-012-0753-y
   PubMed Web of Science ®Google Scholar
• Kangas, B.D., Delatte, M.S., Vemuri, V.K., Thakur, G.A., Nikas, S.P., Subramanian, K.V., Shukla, V.G., Makriyannis, A. & Bergman, J. (2013) Cannabinoid discrimination and antagonism by cb1 neutral and inverse agonist antagonists. Journal of Pharmacology and Experimental Therapeutics, 344: 561–567. doi:10.1124/jpet.112.201962
   PubMed Web of Science ®Google Scholar
• Khan, M.S.I., Nakano, Y., Tachibana, T. & Ueda, H. (2008) Nitric oxide synthase inhibitor attenuates the anorexigenic effect of corticotropin-releasing hormone in neonatal chicks. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 149(3): 325–329. doi:10.1016/j.cbpa.2008.01.011
   PubMed Web of Science ®Google Scholar
• Khan, M.S.I., Tachibana, T., Hasebe, Y., Masuda, N. & Ueda, H. (2007) Peripheral or central administration of nitric oxide synthase inhibitor affects feeding behavior in chicks. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 148: 458–462. doi:10.1016/j.cbpa.2007.06.006
   PubMed Web of Science ®Google Scholar
• Lim, C.T., Kola, B. & Korbonits, M. (2010) AMPK as a mediator of hormonal signalling. Journal of Molecular Endocrinology, 44: 87–97. doi:10.1677/JME-09-0063
   PubMed Web of Science ®Google Scholar
• López, H.H. (2010) Cannabinoid–hormone interactions in the regulation of motivational processes. Hormones and Behavior, 58: 100–110. doi:10.1016/j.yhbeh.2009.10.005
   PubMed Web of Science ®Google Scholar
• Manzanedo, C., Aguilar, M.A., Do Couto, B.R., Rodríguez-Arias, M. & Miñarro, J. (2009) Involvement of nitric oxide synthesis in sensitization to the rewarding effects of morphine. Neuroscience Letters, 464: 67–70. doi:10.1016/j.neulet.2009.08.017
   PubMed Web of Science ®Google Scholar
• Morley, J.E., Farr, S.A., Sell, R.L., Hileman, S.M. & Banks, W.A. (2011) Nitric oxide is a central component in neuropeptide regulation of appetite. Peptides, 32: 776–780. doi:10.1016/j.peptides.2010.12.015
   PubMed Web of Science ®Google Scholar
• Novoseletsky, N., Nussinovitch, A. & Friedman-Einat, M. (2011) Attenuation of food intake in chicks by an inverse agonist of cannabinoid receptor 1 administered by either injection or ingestion in hydrocolloid carriers. General and Comparative Endocrinology, 170: 522–527. doi:10.1016/j.ygcen.2010.11.011
   PubMed Web of Science ®Google Scholar
• Olanrewaju, H.A., Thaxton, J.P., Dozier, W.A., Purswell, J., Roush, W.B. & Branton, S.L. (2006) A review of lighting programs for broiler production. International Journal of Poultry Science, 5(4): 301–308. doi:10.3923/ijps.2006.301.308
   Google Scholar
• Onaivi, E.S., Carpio, O., Ishiguro, H., Schanz, N., Uhl, G.R. & Benno, R. (2008) Behavioral effects of CB2 cannabinoid receptor activation and its influence on food and alcohol consumption. Annals of the New York Academy of Sciences, 1139: 426–433. doi:10.1196/nyas.2008.1139.issue-1
   PubMed Web of Science ®Google Scholar
• Pacher, P. & Mackie, K. (2012) Interplay of cannabinoid 2 (CB2) receptors with nitric oxide synthases, oxidative and nitrative stress, and cell death during remote neurodegeneration. Journal of Molecular Medicine, 90: 347–351. doi:10.1007/s00109-012-0884-1
   PubMed Web of Science ®Google Scholar
• Parker, K.E., Johns, H.W., Floros, T.G. & Will, M.J. (2014) Central amygdala opioid transmission is necessary for increased high-fat intake following 24-h food deprivation, but not following intra-accumbens opioid administration. Behavioural Brain Research, 260: 131–138. doi:10.1016/j.bbr.2013.11.014
   PubMed Web of Science ®Google Scholar
• Pertwee, R.G. (2005) Inverse agonism and neutral antagonism at cannabinoid CB1 receptors. Life Sciences, 76: 1307–1324. doi:10.1016/j.lfs.2004.10.025
   PubMed Web of Science ®Google Scholar
• Riediger, T., Giannini, P., Erguven, E. & Lutz, T. (2006) Nitric oxide directly inhibits ghrelin-activated neurons of the arcuate nucleus. Brain Research, 1125: 37–45. doi:10.1016/j.brainres.2006.09.049
   PubMed Web of Science ®Google Scholar
• Rocchitta, G., Migheli, R., Mura, M.P., Grella, G., Esposito, G., Marchetti, B., Miele, E., Desole, M.S., Miele, M. & Serra, P.A. (2005) Signaling pathways in the nitric oxide and iron-induced dopamine release in the striatum of freely moving rats: role of extracellular Ca2+ and L-type Ca2+ channels. Brain Research, 1047: 18–29. doi:10.1016/j.brainres.2005.04.008
   PubMed Web of Science ®Google Scholar
• Roohbakhsh, A., Hajizadeh Moghaddam, A., Massoudi, R. & Zarrindast, M.R. (2007) Role of dorsal hippocampal cannabinoid receptors and nitric oxide in anxiety like behaviours in rats using the elevated plus-maze test. Clinical and Experimental Pharmacology and Physiology, 34: 223–229. doi:10.1111/j.1440-1681.2007.04576.x
   PubMed Web of Science ®Google Scholar
• Saito, E.S., Kaiya, H., Tachibana, T., Tomonaga, S., Denbow, D.M., Kangawa, K. & Furuse, M. (2005) Inhibitory effect of ghrelin on food intake is mediated by the corticotropin-releasing factor system in neonatal chicks. Regulatory Peptides, 125: 201–208. doi:10.1016/j.regpep.2004.09.003
   PubMed Web of Science ®Google Scholar
• Sharkey, K.A., Darmani, N.A. & Parker, L.A. (2014) Regulation of nausea and vomiting by cannabinoids and the endocannabinoid system. European Journal of Pharmacology, 722: 134–146. doi:10.1016/j.ejphar.2013.09.068
   PubMed Web of Science ®Google Scholar
• Shujaa, N., Zadori, Z.S., Ronai, A.Z., Barna, I., Mergl, Z., Mozes, M.M. & Gyires, K. (2009) Analysis of the effect of neuropeptides and cannabinoids in gastric mucosal defense initiated centrally in the rat. Journal of Physiology and Pharmacology, 60(7): 93–100.
   PubMed Web of Science ®Google Scholar
• Tambaro, S., Tomasi, M.L. & Bortolato, M. (2013) Long-term CB1 receptor blockade enhances vulnerability to anxiogenic-like effects of cannabinoids. Neuropharmacology, 70: 268–277. doi:10.1016/j.neuropharm.2013.02.009
   PubMed Web of Science ®Google Scholar
• Tedesco, L., Valerio, A., Cervino, C., Cardile, A., Pagano, C., Vettor, R., Pasquali, R., Carruba, M.O., Marsicano, G., Lutz, B., Pagotto, U. & Nisoli, E. (2008) Cannabinoid type 1 receptor blockade promotes mitochondrial biogenesis through endothelial nitric oxide synthase expression in white adipocytes. Diabetes, 57: 2028–2036. doi:10.2337/db07-1623
   PubMed Web of Science ®Google Scholar
• Toda, N., Kishioka, S., Hatano, Y. & Toda, H. (2009) Interactions between morphine and nitric oxide in various organs. Journal of Anesthesia, 23: 554–568. doi:10.1007/s00540-009-0793-9
   PubMed Web of Science ®Google Scholar
• Van Tienhoven, A. & Juhasz, L.P. (1962) The chicken telencephalon, diencephalon and mesencephalon in stereotaxic coordinates. The Journal of Comparative Neurology, 118: 185–197. doi:10.1002/(ISSN)1096-9861
   PubMedGoogle Scholar
• Waksman, Y., Olson, J.M., Carlisle, S.J. & Cabral, G.A. (1999) The central cannabinoid receptor (cb1) mediates inhibition of nitric oxide production by rat microglial cells. Journal of Pharmacology and Experimental, 288(3): 1357–1366.
   PubMed Web of Science ®Google Scholar
• Wang, C., Hou, S.S., Huang, W., Xu, T.S., Rong, G.H. & Xie, M. (2014) Arginine affects appetite via nitric oxide in ducks. Poultry Science, 93(8): 2048–2053. doi:10.3382/ps.2013-03812
   PubMed Web of Science ®Google Scholar
• Wittmann, G., Deli, L., Kalló, I., Hrabovszky, E., Watanabe, M., Liposits, Z. & Fekete, C. (2007) Distribution of type 1 cannabinoid receptor (CB1)-immunoreactive axons in the mouse hypothalamus. The Journal of Comparative Neurology, 503: 270–279. doi:10.1002/(ISSN)1096-9861
   PubMed Web of Science ®Google Scholar
• Yang, S.J. & Denbow, D.M. (2007) Interaction of leptin and nitric oxide on food intake in broilers and Leghorns. Physiology & Behavior, 92(4): 651–657. doi:10.1016/j.physbeh.2007.05.009
   PubMed Web of Science ®Google Scholar
• Zendehdel, M., Hasani, K., Babapour, V., Seyedali Mortezaei, S., Khoshbakht, Y. & Hassanpour, S. (2014a) Dopamine-induced hypophagia is mediated by D1 and 5HT-2c receptors in chicken. Veterinary Research Communications, 38: 11–19. doi:10.1007/s11259-013-9581-y
   PubMed Web of Science ®Google Scholar
• Zendehdel, M., Hamidi, F. & Hassanpour, S. (2014b) The effect of histaminergic system on nociceptin/orphanin FQ induced food intake in chicken. International Journal of Peptide Research and Therapeutics, doi:10.1007/s10989-014-9445-5
   Web of Science ®Google Scholar
• Zendehdel, M. & Hassanpour, S. (2014) Ghrelin-induced hypophagia is mediated by the β2 adrenergic receptor in chicken. The Journal of Physiological Sciences, 64: 383–391. doi:10.1007/s12576-014-0330-y
   PubMed Web of Science ®Google Scholar
• Zendehdel, M., Hassanpour, S., Babapour, V., Charkhkar, S. & Mahdavi, M. (2015) Interaction between endocannabinoid and opioidergic systems regulates food intake in neonatal chicken. International Journal of Peptide Research and Therapeutics, doi:10.1007/s10989-015-9457-9
   PubMed Web of Science ®Google Scholar