Arcopallium, NMDA antagonists and ingestive behaviors in pigeons

Physiology and Behavior

Volumn 98, Issue 5, 2009, Pages 594-601

  da Silva, Amanda Alcaraz ^a   de Azevedo Campanella, Luciane Coutinho ^a   Ramos, Mayara Caldas ^a   Parreira, Caroline ^a   Faria, Moacir Serralvo ^a   Marino Neto, José ^a   Paschoalini, Marta Aparecida ^a  

^a FEDERAL UNIVERSITY OF SANTA CATARINA   (Brazil)

Author keywords

Arcopallium intermedium; Food intake; Glutamate; Nucleus taeniae; Pigeons; Water intake

Indexed keywords

6,7 DINITRO 2,3 QUINOXALINEDIONE; ARCOPALLIUM; DIMETHYL SULFOXIDE; DIZOCILPINE; GLUTAMIC ACID; N METHYL DEXTRO ASPARTIC ACID RECEPTOR BLOCKING AGENT; UNCLASSIFIED DRUG;

AMYGDALOID NUCLEUS; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN FUNCTION; CONTROLLED STUDY; FEEDING BEHAVIOR; FLUID INTAKE; FOREBRAIN; MAMMAL; NONHUMAN; PIGEON; PRIORITY JOURNAL;

AMYGDALA; ANALYSIS OF VARIANCE; ANIMALS; COLUMBIDAE; DIZOCILPINE MALEATE; DOSE-RESPONSE RELATIONSHIP, DRUG; DRINKING; EATING; FEEDING BEHAVIOR; MALE; PROSENCEPHALON; QUINOXALINES; REACTION TIME; RECEPTORS, N-METHYL-D-ASPARTATE;

EID: 70349771166     PISSN: 00319384     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.physbeh.2009.09.009     Document Type: Article

References (104)

1. Del Parigi K., Chen A.D., Salbe J.F., Gautier E., Ravussin E.M., and Tataranni P.A. Tasting a liquid meal after a prolonged fast is associated with preferential activation of the left hemisphere. NeuroReport 13 (2002) 1141-1145
2. O'Doherty J.P., Deichmann R., Critchley H.D., and Dolan R.J. Neural responses during anticipation of a primary taste reward. Neuron 33 (2002) 815-826
3. Gottfried J., O'Doherty J.P., and Dolan R.J. Encoding predictive reward value in human amygdala and orbitofrontal cortex. Science 301 (2003) 1104-1107
4. Small D.M., Gerber J.C., Mark Y.E., and Hummel T. Differential neural responses evoked by orthonasal versus retronasal odorant perception in humans. Neuron 47 (2005) 593-605
5. Smeets P.A., de Graaf C., Stafleu A., van Osch M.J., Nievelstein R.A., and van der Grond J. Effect of satiety on brain activation during chocolate tasting in men and women. Am J Clin Nutr 83 (2006) 1297-1305
6. Nakano Y., Oomura Y., Lénárd L., Nishino H., Aou S., Yamamoto T., et al. Feeding-related activity of glucose-and morphine-sensitive neurons in the monkey amygdala. Brain Res 399 (1986) 167-172
7. Rolls E.T. Central nervous mechanisms related to feeding and appetite. Br Med Bull 37 (1981) 131-134
8. Rollins B.L., and King B.M. Amygdala-lesion obesity: what is the role of the various amygdaloid nuclei?. Am J Physiol Regul Integr Comp Physiol 279 (2000) 1348-1356
9. King B.M. Amygdaloid lesion-induced obesity: relation to sexual behavior, olfaction, and the ventromedial hypothalamus. Am J Physiol Regul Integr Comp Physiol 291 (2006) 1201-1214
10. Fonberg E. Hyperphagia produced by lateral amygdala lesions in dogs. Acta Neurobiol Exp 31 (1971) 19-32
11. Green J.D., Clemente C.D., and de Groot J. Rhinencephalic lesions and behavior in cats. J Comp Neurol 108 (1957) 505-545
12. Morgane P.J., and Kosman A.J. Alterations in feline behaviour following bilateral amygdalectomy. Nature 180 (1957) 598-600
13. Morgane P.J., and Kosman A.J. A rhinencephalic feeding center in the cat. Am J Physiol 197 (1959) 158-162
14. Schwartzbaum J.S. Some characteristics of "amygdaloid hyperphagia" in monkeys. Am J Physiol 74 (1961) 252-259
15. Terzian H., and Ore G.D. Syndrome of Kluver and Bucy reproduced in man by bilateral removal of the temporal lobes. Neurology 5 (1955) 373-380
16. Wood C.D. Behavioral changes following discrete lesions of temporal lobe structures. Neurology 8 (1958) 215-220
17. Fonberg E. Aphagia, produced by destruction of the dorsomedial amygdala in dogs. Bull Acad Pol Sci Biol 14 (1966) 719-722
18. Hajnal A., Sandor P., Jando G., Vida I., Czurko A., Karadi Z., et al. Feeding disturbances and EEG activity changes after amygdaleoid kainate lesions in the rat. Brain Res Bull 29 (1992) 909-916
19. Korczynski R., and Fonberg E. Instrumental reactions and food and water intake in medial amygdala rats. Acta Neurobiol Exp 36 (1976) 667-685
20. Box B.M., and Mogenson G.J. Alterations in ingestive behaviors after bilateral lesions of the amygdala in the rat. Physiol Behav 15 (1975) 679-688
21. King B.M., Kass J.M., Cadieux N.L., Sam H., Neville K.L., and Arceneaux E.R. Hyperphagia and obesity in female rats with temporal lobe lesions. Physiol Behav 54 (1993) 759-765
22. King B.M., Kass J.M., Neville K.L., Sam H., Tatford III A.C., and Zansler C.A. Abnormal weight gain in rats with amygdaloid lesions. Physiol Behav 54 (1993) 467-470
23. Rollins B., and King B.M. Amygdala-lesion obesity: what is the role the various amygdaloid nuclei?. Am J Physiol Regul Integr Comp Physiol 279 (2000) 1348-1356
24. King B.M. Amygdaloid lesion-induced obesity: relation to sexual behavior, olfaction, and the ventromedial hypothalamus. Am J Physiol Regul Integr Comp Physiol 291 (2006) 1201-1214
25. Blumberg S., Schroeder M., Haba D., Malkesman O., Torregrossa A.M., Weller A., et al. Effects of CCK-8 on independent ingestion and central c-Fos-like immunoreactivity in rats on postnatal days 10 and 11. Peptides 27 (2006) 2820-2828
26. Becskei C., Grabler V., Edwards G.L., Riediger T., and Lutz T.A. Lesion of the lateral parabrachial nucleus attenuates the anorectic effect of peripheral amylin and CCK. Brain Res 1162 (2007) 76-84
27. Rowland N.E., Crews E.C., and Gentry R.M. Comparison of Fos induced in rat brain by GLP-1 and amylin. Regul Pept 71 (1997) 171-174
28. Smith B.K., York D.A., and Bray G.A. Effects of dietary preference and galanin administration in the paraventricular or amygdaloid nucleus on diet self-selection. Brain Res Bull 39 (1996) 149-154
29. Lin L., and York D.A. Enterostatin actions in the amygdala and PVN to suppress feeding in the rat. Peptides 18 (1997) 1341-1347
30. Vigh J., Lenard L., and Fekete E. Bombesin microinjection into the basolateral amygdala influences feeding behavior in the rat. Brain Res 847 (1999) 253-261
31. Fekete E., Vigh J., Bagi E.E., and Lenard L. Gastrin-releasing peptide microinjected into the amygdala inhibits feeding. Brain Res 955 (2002) 55-63
32. Levine A.S., Olszewski P.K., Mullett M.A., Pomonis J.D., Grace M.K., Kotz C.M., et al. Intra-amygdalar injection of DAMGO: effects on c-Fos levels in brain sites associated with feeding behavior. Brain Res 1015 (2004) 9-14
33. Primeaux S.D., York D.A., and Bray G.A. Neuropeptide Y administration into the amygdala alters high fat food intake. Peptides 27 (2006) 1644-1651
34. Fekete E.M., Bagi E.E., Toth K., and Lenard L. Neuromedin C microinjected into the amygdala inhibits feeding. Brain Res Bull 71 (2007) 386-392
35. Tóth K., László K., Bagi E.E., Lukács E., and Lénárd L. Effects of intraamygdaloid microinjections of acylated-ghrelin on liquid food intake of rats. Brain Res Bull 77 (2008) 105-111
36. Lenard L., Hahn Z., and Karadi Z. Body weight changes after neurochemical manipulations of lateral amygdala: noradrenergic and dopaminergic mechanisms. Brain Res 249 (1982) 95-101
37. Parker G.C., Bishop C., and Coscina D.V. Estrous cycle and food availability affect feeding induced by amygdala 5-HT receptor blockade. Pharmacol Biochem Behav 71 (2002) 701-707
38. Lee S.W., and Stanley B.G. NMDA receptors mediate feeding elicited by neuropeptide Y in the lateral and perifornical hypothalamus. Brain Res 1063 (2005) 1-8
39. Stanley B.G., Willett V.L., Donias H.W., Ha L.H., and Spears L.C. The lateral hypothalamus: a primary site mediating excitatory amino acid-elicited eating. Brain Res 630 (1993) 41-49
40. Stanley B.G., Ha L.H., Spears L.C., and Dee M.G. Lateral hypothalamus injections of glutamate, kainic acid, d, l-alpha-amino-3-hydroxy-5-methyl-isoxazole propionic acid or N-methyl-d-aspartic acid rapidly elicit intense transient eating in rats. Brain Res 613 (1993) 88-95
41. Stanley B.G., Willett V.L., Donias H.W., Dee M.G., and Duva M.A. Lateral hypothalamus NMDA receptors and glutamate as physiological mediators of eating and weight control. Am J Physiol 270 (1996) 443-449
42. Stanley B.G., Butterfield B.S., and Grewal R.S. NMDA receptor coagonist glycine site: evidence for a role in lateral hypothalamic stimulation of feeding. Am J Physiol 273 (1997) R790-R796
43. Kelley A.E., and Swanson C.J. Feeding induced by blockade of AMPA and kainite receptors within the ventral striatum: a microinfusion mapping study. Behav Brain Res 89 (1997) 107-113
44. Rada P., Tucci S., Murzi E., and Hernandéz L. Extracelular glutamate increases in the lateral hypothalamus and decrease in the nucleus accumbens during feeding. Brain Res 768 (1997) 338-340
45. Saulskaya N.B., and Mikhailova M.O. Feeding-induced decrease in extracelular glutamate level in the rat nucleus accumbens: dependence on glutamate uptake. Neuroscience 112 (2002) 791-801
46. Zeni L.R., Seidler H.B.K., De Carvalho N.A.S., Freitas C.G., Marino-Neto J., and Paschoalini M.A. Glutamatergic control of food intake in pigeons: effects of central injections of glutamate, NMDA, and AMPA receptor agonists and antagonists. Pharmacol Biochem Behav 65 (2000) 67-74
47. Da Silva A.A., Marino-Neto J., and Paschoalini M.A. Feeding induced by microinjections of NMDA and AMPA-kainate receptor antagonists into ventral striatal and ventral pallidal areas of the pigeons. Brain Res 996 (2003) 76-83
48. Da Silva A.A., Campanella L.C., Ramos M.C., Farias M.S., Paschoalini M.A., and Marino-Neto J. Ingestive effects of NMDA and AMPA-kainate receptor antagonists microinjections into the lateral hypothalamus of the pigeons (Columba livia). Brain Res 1115 (2006) 75-82
49. Reiner A., Perkel D.J., Bruce L.L., Butler A.B., Csillag A., Kuenzel W., et al. Revised nomenclature for avian telecephalon and some related brainstem nuclei. J Comp Neurol 473 (2004) 377-414
50. Yamamoto K., Sun Z., Wang H.B., and Reiner A. Subpallial amygdala and nucleus taeniae in birds resemble extended amygdala and medial amygdala in mammals in their expression of markers of regional identity. Brain Res Bull 66 (2005) 341-347
51. Reiner A., and Karten H.J. Comparison of olfactory bulb projections in pigeons and turtles. Brain Behav 27 (1985) 11-27
52. Canteras N.S., Simerly R.B., and Swanson L.W. Organization of projections from the medial nucleus of the amygdale: a PHAL study in the rat. J Comp Neurol 360 (1995) 213-245
53. Casini G., Bingman V.P., and Bagnoli P. Connections of the pigeon dorsomedial forebrain studied with WGA-HRP and 3H-proline. J Comp Neurol 245 (1986) 454-470
54. Cheng M., Chaiken M., Zuo M., and Miller H. Nucleus taeniae of the amygdale of birds: anatomical and fuctional studies in ring doves (Streptopelia risoria) and European starlings (Sturnus vulgaris). Brain Behav 53 (1999) 243-270
55. Balthazart J., Foidart A., Houbart M., Prins G.S., and Ball G.F. Distribution of androgen receptor-immunoreactive cells in the quail forebrain and their relationship with aromatase immunoreactivity. J Neurobiol 35 (1998) 323-340
56. Balthazart J., Foidart A., Houbart M., Prins G.S., and Ball G.F. Immunocytochemical localization of androgen receptors in the male songbird and quail brain. J Comp Neurol 317 (1992) 407-420
57. Bernard D.J., Bentley G.E., Balthazart J., Turek F.W., and Ball G.F. Androgen receptor, estrogen receptor alpha, and estrogen receptor beta show distict patterns of expression in forebrain song control nuclei of European starlings. Endocrinology 140 (1999) 4633-4643
58. Martinez-Vargas M.C., Stumpf W.E., and Sar M. Anatomical distribution of estrogen target cells in the avian CNS: a comparison with the mammalian CNS. J Comp Neurol 167 (1976) 83-103
59. Absil P., Braquenier J.B., Balthazart J., and Ball G.F. Effects of lesions of nucleus taeniae on appetitive and consummatory aspects of male sexual behavior in Japanese quail. Brain Behav Evol 60 (2002) 13-35
60. Thompson R.R., Goodson J.L., Ruscio M.G., and Adkins-Regan E. Role of the archistriatal nucleus taeniae in the sexual behavior of male Japanese quail (Coturnix japonica): a comparison of function with the medial nucleus of the amygdale in mammals. Brain Behav 51 (1998) 215-229
61. Cornil C., Foidart A., Minet A., and Balthazart J. Immunocytochemical localization of ionotropic glutamate receptors subunits in the adult quail forebrain. J Comp Neurol 428 (2000) 577-608
62. Gibbs M.E., Johnston A.N., Mileusnic R., and Criwe S.F. A comparison of protocols for passive and discriminative avoidance learning tasks in the domestic chick. Brain Res Bull 76 (2008) 198-207
63. Butler A.B. Evolution of brains, cognition and consciousness. Brain Res Bull 75 (2008) 442-449
64. Sun Z., Wang H.B., Laverghetta A., Yamamoto K., and Reiner A. The distribution and cellular localization of glutamic acid decarboxylase-65 (GAD65) mRNA in the forebrain and midbrain of domestic chick. J Chem Neuroanat 29 (2005) 265-281
65. Martinez-García F., Novejarque A., and Lanuza E. Two interconnected functional systems in the amygdala of amniote vertebrales. Brain Res Bull 75 (2008) 206-213
66. Kleven M.S., and Koek W. Discriminative stimulus effects of 8-hydroxy-2-(di-n-propylamino) tetralin in pigeon and rats: species similarities and differences. J Pharmacol Exp Ther 284 (1998) 238-249
67. Barret J.E., Zhang L., Gleeson S., and Gamble E.H. Anxiolytic and antidepressant mechanisms of 5-HT1A drugs in the pigeon: contributions from behavioral studies. Neurosci Biobehav Rev 18 (1994) 73-83
68. Barbato G.F. Genetic control of food intake in chickens. J Nutr 124 (1994) 1341-1348
69. Kuenzel W.J., and Blähser S. Vasoactive intestinal polypeptide (VIP)-containing neurons: distribution throughout the brain of the chick (Galllus domesticus) with focus upon the lateral septal organ. Cell Tissue Res 275 (1994) 91-107
70. Kruzelock R.P., and Barbato G.F. Genotype differences in catecholamine concentrations in hypothalamus intramedial hyperstriatum ventrale and optic tectum of newly hatched chicks. Neurochem Res 16 (1991) 105-112
71. Karten H.J., and Hodos W.A. A stereotaxic atlas of the brain of the pigeon (Columba livia) (1967), Johns Hopkins Press, Baltimore, Maryland
72. Canelo M., Ravazio M.R., Paschoalini M.A., and Marino-Neto J. Food deprivation vs. intraventricular adrenaline. Induced feeding and postprandial behaviors in the pigeons (Columba livia). Physiol Behav 84 (1993) 1075-1079
73. Dario A.J.S., Lopes P.R.C., Freitas C.G., Paschoalini M.A., and Marino-Neto J. Electrografic patterns of postprandial sleep after food deprivation or intraventricular adrenaline injections in pigeons. Brain Res Bull 39 (1996) 249-254
74. Gelsema A.J., McKitrick D.J., and Calaresu F.R. Cardiovascular responses to chemical and electrical stimulation of amygdale in rats. Am J Physiol 253 (1987) 712-718
75. Gentil C.G., Peres V.L., Tufik S., Antunes-Rodrigues J., and Covian M.R. Effects of electrical and chemical stimulation of the central nervous system on sodium chloride and water intake. Acta Physiol Lat Am Supl 23 (1973) 475-476
76. Galaverna O., De Luca Jr. L.A., Schulkin J., Yao S.Z., and Epstein A.N. Deficits in NaCl ingestion after damage to the central nucleus of the amygdala in the rat. Brain Res Bull 28 (1992) 89-98
77. Zardetto-Smith A.M., Beltz T.G., and Johnson A.K. Role of the central nucleus of the amygdala and bed nucleus of the stria terminalis in experimentally-induced salt appetite. Brain Res 645 (1994) 123-134
78. Godino A., Giusti-Paiva A., Antunes-Rodrigues J., and Vivas L. Neurochemical brain groups activated after an isotonic blood volume expansion in rats. Neuroscience 133 (2005) 493-505
79. Margatho L.O., Godino A., Oliveira F.R., Vivas L., and Antunes-Rodrigues J. Lateral parabrachial afferent areas and serotonin mechanisms activated by volume expansion. J Neurosci Res 86 (2008) 3613-3621
80. Margatho L.O., Elias L.L.K., and Antunes-Rodrigues J. GABA in the central amygdaloid nucleus modulates the electrolyte excretion and hormonal responses to blood volume expansion in rats. Braz J Med Biol Res 42 (2009) 114-121
81. Wieroñska J.M., Stachowicz K., Klodziñska M., Smialowska M., and Pilc A. Intraamygdaloid administration of BIBO 3304 increases water intake and extends anxiolytic effects. Pol J Pharmacol 56 (2004) 867-870
82. Synnayah P., Blair-West J.R., McBurnie M.I., McKinley M.J., Oldfield B.J., Rivier J., et al. The effect of urocortin on ingestive behaviours and brain Fos immunoreactivity in mice. Eur J NeuroSci 18 (2003) 373-382
83. Hagiwara Y., Nishigori Y., Fukumori R., and Kubo T. The medial amygdaloid area is envolved in activation of angiotensin II-sensitive neurons in the hypothalamic area. Brain Res 1033 (2005) 128-134
84. Maldonado-Irizarry C.S., Swanson C.J., and Kelley A.E. Glutamate receptors in the nucleus accumbens shell control feeding behavior via lateral hypothalamus. J Neurosci 10 (1995) 6779-6788
85. Reynolds S.M., and Berridge K.C. Glutamate motivational ensembles in nucleus accumbens: rostrocaudal shell gradients of fear and feeding. Eur J NeuroSci 17 (2003) 2187-2200
86. Blevins J.E., Stanley B.G., and Reidelberger R.D. DMSO as a vehicle for central injections: tests with feeding elicited by norepinephrine injected into the paraventricular nucleus. Pharmacol Biochem Behav 71 (2002) 277-282
87. Matheus M.G., and Guimarães F.S. Antagonism of non-NMDA receptors in the dorsal periaqueductal grey induces anxiolytic effect in the elevated plus maze. Psychopharmacology 132 (1997) 14-18
88. Tsvyetlynska N.A., Hill R.H., and Grillner S. Role of AMPA receptor desensitization and the side effects of a DMSO vehicle on reticulospinal EPSPs and locomotor activity. Neurophysiol 94 (2005) 3951-3960
89. Lu C., and Mattson M.P. Dimethyl sulfoxide suppresses NMDA-and AMPA-induced ion currents and calcium influx and protects against excitotoxic death in hippocampal neurons. Exp Neurol 170 (2001) 180-185
90. Fekete E.M., Inoue K., Zhao Y., Rivier J.E., Vale W.W., Szucs A., et al. Delayed satiety-like actions and altered feeding microstructure by a selective type 2 corticotropin-releasing factor agonist in rats: intra-hypothalamic urocortin 3 administration reduces food intake by prolonging the post-meal interval. Neuropsychopharmacology 32 (2007) 1052-1068
91. Diekamp B., Gagliardo A., and Güntürkün O. Nonspatial and subdivision-specific working memory deficits after selective lesions of the avian prefrontal cortex. J Neurosci 22 (2002) 9573-9580
92. Güntürkün O. The avian 'prefrontal cortex' and cognition. Cur Opin Neurobiol 15 (2005) 686-693
93. Kalenscher T., Windmann S., Diekamp B., Rose J., Güntürkün O., and Colombo M. Single units in the pigeon brain integrate reward amount and time-to-reward in an impulsive choice task. Cur Biol 15 (2005) 594-602
94. Lowndes M., Davies D.C., and Johnson M.H. Archistriatal lesions impair the acquisition of filial preferences during imprinting in the domestic chick. Eur J Neurosci 6 (1994) 1143-1148
95. Lowndes M., and Davies D.C. The effects of archistriatal lesions on one-trial passive avoidance learning in the chick. Eur J NeuroSci 6 (1994) 525-530
96. Aoki N., Izawa E., Yanagihara S., and Matsushima T. Neural correlates of memorized associations and cued movements in archistriatum of the domestic chick. Eur J NeuroSci 17 (2003) 1935-1946
97. Aoki N., Csillag A., and Matsushima T. Localized lesions of arcopallium intermedium of the lateral forebrain caused a handling-cost aversion in the domestic chick performing a binary choice task. Eur J NeuroSci 24 (2006) 2314-2326
98. Matsushima T., Kawamori A., and Bem-Sojka T. Neuro-economics in chicks: foraging choices based on amount, delay and cost. Brain Res Bull 76 (2008) 245-252
99. Davies D.C., Csillag A., Szekely A.D., and Kabai P. Efferent connections of the domestic chick archistriatum: a phaseolus lectin anterograde tracing study. J Comp Neurol 389 (1997) 679-693
100. Veenman C.L., Wild J.M., and Reiner A. Organization of the avian "corticostriatal" projection system: a retrograde and anterograde pathway tracing study in pigeon. J Comp Neurol 354 (1995) 87-126
101. Martínez-García F., Martínez-Marcos A., and Lanuza E. The pallial amygdala of amniote vertebrales: evolution on the concept, evolutions of the structure. Brain Res Bull 57 (2002) 463-469
102. Zeier H., and Karten H.J. The archistriatum of the pigeon: organization of afferent and efferent connections. Brain Res 31 (1971) 313-326
103. Atoji Y., and Wild J.M. Fiber connections of the hippocampal formation and septum and subdivisions of the hippocampal formation in the pigeons as revealed by tract tracing and kainic acid lesions. J Com Neurol 475 (2004) 426-461
104. Campanella L.C., Silva A.A., Gellert D.S., Parreira C., Ramos M.C., Paschoalini M.A., et al. Tonic serotonergic control of ingestive behaviours in the pigeon (Columba livia): The role of the arcopallium. Behav Brain Res (2009) [available online 24 July 2009, Electronic publication ahead of print]