Literature DB >> 26362886

Critical role of the neural pathway from the intermediate medial mesopallium to the intermediate hyperpallium apicale in filial imprinting of domestic chicks (Gallus gallus domesticus).

N Aoki1, S Yamaguchi1, T Kitajima1, A Takehara1, S Katagiri-Nakagawa1, R Matsui2, D Watanabe2, T Matsushima3, K J Homma4.   

Abstract

Filial imprinting in precocial birds is a useful model for studying early learning and cognitive development, as it is characterized by a well-defined sensitive or critical period. We recently showed that the thyroid hormone 3,5,3'-triiodothyronine (T3) determines the onset of the sensitive period. Moreover, exogenous injection of T3 into the intermediate medial mesopallium (IMM) region (analogous to the associative cortex in mammals) enables imprinting even on post-hatch day 4 or 6 when the sensitive period has been terminated. However, the neural mechanisms downstream from T3 action in the IMM region remain elusive. Here, we analyzed the functional involvement of the intermediate hyperpallium apicale (IMHA) in T3 action. Bilateral excitotoxic ablation of the IMHA prevented imprinting in newly hatched chicks, and also suppressed the recovery of the sensitive period by systemic intra-venous or localized intra-IMM injection of T3 in day-4 chicks. In contrast to the effect in the IMM, direct injection of T3 into the IMHA did not enable imprinting in day-4 chicks. Moreover, bilateral ablation of IMHA after imprinting training impaired recall. These results suggest that the IMHA is critical for memory acquisition downstream following T3 action in the IMM and further, that it receives and retains information stored in the IMM for recall. Furthermore, both an avian adeno-associated viral construct containing an anterograde tracer (wheat-germ agglutinin) and a retrograde tracer (cholera toxin subunit B) revealed neural connections from the IMM to the IMHA. Taken together, our findings suggest that hierarchical processes from the primary area (IMM) to the secondary area (IMHA) are required for imprinting.
Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  critical period; filial imprinting; memory priming; memory trace; sensitive period; thyroid hormone

Mesh:

Substances:

Year:  2015        PMID: 26362886     DOI: 10.1016/j.neuroscience.2015.09.014

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  5 in total

1.  Expression of oxytocin receptors in the zebra finch brain during vocal development.

Authors:  Matthew T Davis; Kathleen E Grogan; Isabel Fraccaroli; Timothy J Libecap; Natalie R Pilgeram; Donna L Maney
Journal:  Dev Neurobiol       Date:  2021-12-04       Impact factor: 3.964

2.  Imprintability of Newly Hatched Domestic Chicks on an Artificial Object: A Novel High Time-Resolution Apparatus Based on a Running Disc.

Authors:  Naoya Aoki; Chihiro Mori; Toshiyuki Fujita; Shouta Serizawa; Shinji Yamaguchi; Toshiya Matsushima; Koichi J Homma
Journal:  Front Physiol       Date:  2022-03-11       Impact factor: 4.566

3.  Combined predisposed preferences for colour and biological motion make robust development of social attachment through imprinting.

Authors:  Momoko Miura; Daisuke Nishi; Toshiya Matsushima
Journal:  Anim Cogn       Date:  2019-11-11       Impact factor: 2.899

4.  Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting.

Authors:  Giorgi Margvelani; Maia Meparishvili; Tamar Kiguradze; Brian J McCabe; Revaz Solomonia
Journal:  Sci Rep       Date:  2018-11-28       Impact factor: 4.379

5.  A high sensitivity ZENK monoclonal antibody to map neuronal activity in Aves.

Authors:  Gregory Charles Nordmann; Erich Pascal Malkemper; Lukas Landler; Lyubov Ushakova; Simon Nimpf; Robert Heinen; Stefan Schuechner; Egon Ogris; David Anthony Keays
Journal:  Sci Rep       Date:  2020-01-22       Impact factor: 4.379

  5 in total

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