Contact-call driven and tone-driven zenk expression in the nucleus ovoidalis of the budgerigar (Melopsittacus undulatus)

NeuroReport

Volumn 17, Issue 13, 2006, Pages 1407-1410

  Brauth, Steven E ^a   Liang, Wenru ^a   Hall, William S ^a  

^a UNIVERSITY OF MARYLAND   (United States)

Author keywords

Auditory perception; egr 1; Immediate early gene; Vocal learning

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; AUDITORY STIMULATION; GENE EXPRESSION; HEARING; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; TELENCEPHALON; THALAMUS; VISION;

ACOUSTIC STIMULATION; ANIMAL COMMUNICATION; ANIMALS; AUDITORY PATHWAYS; EARLY GROWTH RESPONSE PROTEIN 1; GENE EXPRESSION; GENE EXPRESSION REGULATION; IMMUNOHISTOCHEMISTRY; MELOPSITTACUS; SOUND SPECTROGRAPHY; THALAMIC NUCLEI;

EID: 33748048132     PISSN: 09594965     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.wnr.0000233105.28279.fa     Document Type: Article

References (23)

1. Brauth SE, Reiner A. Calcitonin-gene related peptide is an evolutionarily conserved marker within the amniote thalamo-telencephalic auditory pathway. J Comp Neurol 1991; 313:227-239.
2. Durand SE, Brauth SE, Liang W. Calcitonin gene-related peptide immunoreactive cells and fibers in forebrain vocal and auditory nuclei of the budgerigar (Melopsittacus undulatus). Brain Behav Evol 2001; 58:61-79.
3. Durand SE, Tepper JM, Cheng MF. The shell region of the nucleus ovoidalis: a subdivision of the avian auditory thalamus. J Comp Neurol 1992; 323:495-518.
4. Lanuza E, Davies DC, Landete JM, Novejarque A, Martinez-Garcia F. Distribution of CGRP-like immunoreactivity in the chick and quail brain. J Comp Neurol 2000; 421:515-532.
5. Martinez-Garcia F, Novejarque A, Landete JM,Moncho-Bogani J, Lanuza E. Distribution of calcitonin gene-related peptide-like immunoreactivity in the brain of the lizard Podarcis hispanica. J Comp Neurol 2002; 447:99-113.
6. Zeng SJ, Zhang XW, Peng WM, and Zuo MX. Immunohistochemistry and neural connectivity of the Ov shell in the songbird and their evolutionary implications. J Comp Neurol 2004; 470:192-209.
7. Coolen LM, Veening JG, Petersen DW, Shipley MT. Parvocellular subparafascicular thalamic nucleus in the rat: anatomical and functional compartmentalization. J Comp Neurol 2003; 463:117-131.
8. Linke R, Braune G, Schwegler H. Differential projection of the posterior paralaminar thalamic nuclei to the amygdaloid complex in the rat. Exp Brain Res 2000; 134:520-532.
9. Linke R, Schwegler H. Convergent and complementary projections of the caudal paralaminar thalamic nuclei to rat temporal and insular cortex. Cereb Cortex 2000; 10:753-771.
10. Karten HJ. The ascending auditory pathway in the pigeon (Columba livia). II. Telencephalic projections of the nucleus ovoidalis thalami. Brain Res 1968; 11:134-153.
11. Wild JM, Karten HJ, Frost BJ. Connections of the auditory forebrain in the pigeon (Columba livia). J Comp Neurol 1993; 337:32-62.
12. Bigalke-Kunz B, Rubsamen R, Dorrscheidt GJ. Tonotopic organization and functional characterization of the auditory thalamus in a songbird, the European starling. J Comp Physiol [A] 1987; 161:255-265.
13. Bonke BA, Bonke D, Scheich H. Connectivity of the auditory forebrain nuclei in the guinea fowl (Numida meleagris).Cell Tissue Res 1979; 200:101-121.
14. Brauth SE, McHale CM. Auditory pathways in the budgerigar. II. Intratelencephalic pathways. Brain Behav Evol 1988; 32:193-207.
15. Brauth SE, McHale CM, Brasher CA, Dooling RJ. Auditory pathways in the budgerigar. I. Thalamo-telencephalic projections. Brain Behav Evol 1987; 30:174-199.
16. Striedter GF. The vocal control pathways in budgerigars differ from those in songbirds. J Comp Neurol 1994; 343:35-56.
17. Hile AG, Plummer TK, Striedter GF. Male vocal imitation produces call convergence during pair bonding in budgerigars, Melopsittacus undulatus. Anim Behav 2000; 59:1209-1218.
18. Jarvis ED, Mello CV. Molecular mapping of brain areas involved in parrot vocal communication. J Comp Neurol 2000; 419:1-31.
19. Brauth S, Liang W, Roberts TF, Scott LL, Quinlan EM. Contact call-driven Zenk protein induction and habituation in telencephalic auditory pathways in the budgerigar (Melopsittacus undulatus): implications for understanding vocal learning processes. Learn Mem 2002; 9:76-88.
20. Brauth SE, LiangW, Beru Y, Roberts TF, Hall WS. Feeding and contact call stimulation both induce zenk and cfos expression in a higher order telencephalic area necessary for vocal learning in budgerigars. Behav Brain Res 2006; 168:331-338.
21. Dooling RJ, Brown SD, Park TJ, Okanoya K, Soli SD. Perceptual organization of acoustic stimuli by budgerigars (Melopsittacus undulatus): I. Pure tones. J Comp Psychol 1987a; 101:139-149.
22. Dooling RJ, Park TJ, Brown SD, Okanoya K, Soli SD. Perceptual organization of acoustic stimuli by budgerigars (Melopsittacus undulatus): II. Vocal signals. J Comp Psychol 1987b; 101:367-381.
23. Scheich H, Bonke BA. Tone-versus FM-induced patterns of excitation and suppression in the 14-C-2-deoxyglucose labeled auditory 'cortex' of the guinea fowl. Exp Brain Res 1981; 44:445-449.