Segado Melanie, Hollinger Avrum, Thibodeau Joseph, Penhune Virginia, Zatorre Robert J
Montreal Neurological Institute, Montreal, QC, Canada.
BRAMS International Laboratory for Brain, Music, and Sound Research, Montreal, QC, Canada.
Front Neurosci. 2018 May 28;12:351. doi: 10.3389/fnins.2018.00351. eCollection 2018.
This research uses an MR-Compatible cello to compare functional brain activation during singing and cello playing within the same individuals to determine the extent to which arbitrary auditory-motor associations, like those required to play the cello, co-opt functional brain networks that evolved for singing. Musical instrument playing and singing both require highly specific associations between sounds and movements. Because these are both used to produce musical sounds, it is often assumed in the literature that their neural underpinnings are highly similar. However, singing is an evolutionarily old human trait, and the auditory-motor associations used for singing are also used for speech and non-speech vocalizations. This sets it apart from the arbitrary auditory-motor associations required to play musical instruments. The pitch range of the cello is similar to that of the human voice, but cello playing is completely independent of the vocal apparatus, and can therefore be used to dissociate the auditory-vocal network from that of the auditory-motor network. While in the MR-Scanner, 11 expert cellists listened to and subsequently produced individual tones either by singing or cello playing. All participants were able to sing and play the target tones in tune (<50C deviation from target). We found that brain activity during cello playing directly overlaps with brain activity during singing in many areas within the auditory-vocal network. These include primary motor, dorsal pre-motor, and supplementary motor cortices (M1, dPMC, SMA),the primary and periprimary auditory cortices within the superior temporal gyrus (STG) including Heschl's gyrus, anterior insula (aINS), anterior cingulate cortex (ACC), and intraparietal sulcus (IPS), and Cerebellum but, notably, exclude the periaqueductal gray (PAG) and basal ganglia (Putamen). Second, we found that activity within the overlapping areas is positively correlated with, and therefore likely contributing to, both singing and playing in tune determined with performance measures. Third, we found that activity in auditory areas is functionally connected with activity in dorsal motor and pre-motor areas, and that the connectivity between them is positively correlated with good performance on this task. This functional connectivity suggests that the brain areas are working together to contribute to task performance and not just coincidently active. Last, our findings showed that cello playing may directly co-opt vocal areas (including larynx area of motor cortex), especially if musical training begins before age 7.
本研究使用一台与磁共振成像(MR)兼容的大提琴,比较同一受试者在唱歌和演奏大提琴时大脑的功能激活情况,以确定像演奏大提琴所需的那种任意听觉 - 运动关联在多大程度上会占用为唱歌而进化的功能性脑网络。演奏乐器和唱歌都需要声音与动作之间高度特定的关联。由于二者都用于产生音乐声音,文献中常常假定它们的神经基础高度相似。然而,唱歌是人类一种古老的进化特征,用于唱歌的听觉 - 运动关联也用于言语和非言语发声。这使其有别于演奏乐器所需的任意听觉 - 运动关联。大提琴的音域与人声相似,但演奏大提琴完全不依赖于发声器官,因此可用于区分听觉 - 发声网络和听觉 - 运动网络。在磁共振成像扫描仪中,11位专业大提琴演奏者聆听并随后通过唱歌或演奏大提琴发出各个音调。所有参与者都能够准确唱出和奏出目标音调(与目标偏差<50音分)。我们发现,在听觉 - 发声网络的许多区域中,演奏大提琴时的大脑活动与唱歌时的大脑活动直接重叠。这些区域包括初级运动皮层、背侧前运动皮层和辅助运动皮层(M1、dPMC、SMA),颞上回(STG)内的初级和周边初级听觉皮层,包括颞横回、前岛叶(aINS)、前扣带回皮层(ACC)和顶内沟(IPS),以及小脑,但值得注意地排除了导水管周围灰质(PAG)和基底神经节(壳核)。其次,我们发现重叠区域内的活动与通过表现测量确定的唱歌和准确演奏均呈正相关,因此可能对二者都有贡献。第三,我们发现听觉区域的活动与背侧运动和前运动区域的活动在功能上相连,并且它们之间连接性与该任务的良好表现呈正相关。这种功能连接表明这些脑区共同协作以促进任务表现,而不仅仅是同时活跃。最后,我们的研究结果表明,演奏大提琴可能会直接占用发声区域(包括运动皮层的喉部区域),特别是如果音乐训练在7岁之前开始的话。