Abstract

Birdsong learning, like human speech, depends on the early memorization of auditory models, yet how initial auditory experiences are formed and consolidated is unclear. In songbirds, a putative cortical locus is the caudomedial nidopallium (NCM), and one mechanism to facilitate auditory consolidation is 17β-estradiol (E2), which is associated with human speech-language development, and is abundant in both NCM and human temporal cortex. Circulating and NCM E2 levels are dynamic during learning, suggesting E2’s involvement in encoding recent auditory experiences. Therefore, we tested this hypothesis in juvenile male songbirds using a comprehensive assessment of neuroanatomy, behavior, and neurophysiology. First, we found that brain aromatase expression, and thus the capacity to synthesize neuroestrogens, remains high in the auditory cortex throughout development. Further, while systemic estrogen synthesis blockade suppressed juvenile song production, neither systemic nor unilateral E2 synthesis inhibition in NCM disrupted eventual song imitation. Surprisingly, early life neuroestrogen synthesis blockade in NCM enhanced the neural representations of both the birds’ own song and the tutor song in NCM and a downstream sensorimotor region, HVC, respectively. Taken together, these findings indicate that E2 plays a multifaceted role during development, and that, contrary to prediction, tutor song memorization is unimpaired by unilateral estrogen synthesis blockade in the auditory cortex.

Highlights

  • Birdsong learning, like human speech, depends on the early memorization of auditory models, yet how initial auditory experiences are formed and consolidated is unclear

  • We first sought to confirm the presence of aromatase in NCM across development

  • Our collective findings indicate that while aromatase is present in developing auditory cortex, systemic and unilateral attenuation of neuroestrogen production does not impair tutor song memorization

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Summary

Introduction

Like human speech, depends on the early memorization of auditory models, yet how initial auditory experiences are formed and consolidated is unclear. The predominant estrogen 17β-estradiol (E2) is a candidate neuromodulator required for auditory memory consolidation, as is evident in a similar role in adult hippocampal-dependent cognition, across taxa[12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28], but see[29] Both circulating and brain-derived estrogens (‘neuroestrogens’) typically enhance hearing in non-human animals[30,31], and estrogens are associated. Current evidence suggests that neuroestrogen signaling may facilitate the consolidation of recent auditory experience[37]

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