Alward Beau A, Balthazart Jacques, Ball Gregory F
Department of Psychological and Brain Sciences, Johns Hopkins University, Baltimore, Maryland 21218,
Department of Psychology, University of Maryland, College Park, College Park, Maryland 20742, and.
J Neurosci. 2017 Sep 6;37(36):8612-8624. doi: 10.1523/JNEUROSCI.3371-16.2017. Epub 2017 Aug 14.
The neural basis of how learned vocalizations change during development and in adulthood represents a major challenge facing cognitive neuroscience. This plasticity in the degree to which learned vocalizations can change in both humans and songbirds is linked to the actions of sex steroid hormones during ontogeny but also in adulthood in the context of seasonal changes in birdsong. We investigated the role of steroid hormone signaling in the brain on distinct features of birdsong using adult male canaries (), which show extensive seasonal vocal plasticity as adults. Specifically, we bilaterally implanted the potent androgen receptor antagonist flutamide in two key brain regions that control birdsong. We show that androgen signaling in the motor cortical-like brain region, the robust nucleus of the arcopallium (RA), controls syllable and trill bandwidth stereotypy, while not significantly affecting higher order features of song such syllable-type usage (i.e., how many times each syllable type is used) or syllable sequences. In contrast, androgen signaling in the premotor cortical-like brain region, HVC (proper name), controls song variability by increasing the variability of syllable-type usage and syllable sequences, while having no effect on syllable or trill bandwidth stereotypy. Other aspects of song, such as the duration of trills and the number of syllables per song, were also differentially affected by androgen signaling in HVC versus RA. These results implicate androgens in regulating distinct features of complex motor output in a precise and nonredundant manner. Vocal plasticity is linked to the actions of sex steroid hormones, but the precise mechanisms are unclear. We investigated this question in adult male canaries (), which show extensive vocal plasticity throughout their life. We show that androgens in two cortex-like vocal control brain regions regulate distinct aspects of vocal plasticity. For example, in HVC (proper name), androgens regulate variability in syntax but not phonology, whereas androgens in the robust nucleus of the arcopallium (RA) regulate variability in phonology but not syntax. Temporal aspects of song were also differentially affected by androgen signaling in HVC versus RA. Thus, androgen signaling may reduce vocal plasticity by acting in a nonredundant and precise manner in the brain.
习得的发声在发育过程中和成年期如何变化的神经基础是认知神经科学面临的一项重大挑战。人类和鸣禽中习得发声的可变化程度的这种可塑性,在个体发育过程中与性类固醇激素的作用有关,在成年期也与鸟鸣季节性变化背景下的性类固醇激素作用有关。我们使用成年雄性金丝雀()研究了大脑中类固醇激素信号传导对鸟鸣不同特征的作用,成年雄性金丝雀表现出广泛的季节性发声可塑性。具体而言,我们在控制鸟鸣的两个关键脑区双侧植入了强效雄激素受体拮抗剂氟他胺。我们发现,在类似运动皮层的脑区,即古纹状体粗核(RA)中,雄激素信号传导控制音节和颤音带宽的刻板性,而对歌曲的高阶特征,如音节类型使用情况(即每种音节类型使用的次数)或音节序列没有显著影响。相比之下,在前运动皮层样脑区HVC(专有名称)中,雄激素信号传导通过增加音节类型使用情况和音节序列的变异性来控制歌曲的变异性,而对音节或颤音带宽的刻板性没有影响。歌曲的其他方面,如颤音的持续时间和每首歌曲的音节数量,也受到HVC和RA中雄激素信号传导的不同影响。这些结果表明雄激素以精确且非冗余的方式调节复杂运动输出的不同特征。发声可塑性与性类固醇激素的作用有关,但具体机制尚不清楚。我们在成年雄性金丝雀()中研究了这个问题,成年雄性金丝雀一生都表现出广泛的发声可塑性。我们发现,在两个类似皮层的发声控制脑区中,雄激素调节发声可塑性的不同方面。例如,在HVC(专有名称)中,雄激素调节句法的变异性但不调节音系学的变异性,而在古纹状体粗核(RA)中,雄激素调节音系学的变异性但不调节句法的变异性。歌曲的时间方面也受到HVC和RA中雄激素信号传导的不同影响。因此,雄激素信号传导可能通过在大脑中以非冗余且精确的方式起作用来降低发声可塑性。