DeVoogd T J
J Neurobiol. 1986 May;17(3):177-201. doi: 10.1002/neu.480170305.
Following the pioneering work of Nottebohm, the brain regions involved in song production in songbirds have become a focus of extensive research in several laboratories. As both singing behavior and the neuroanatomy of song control regions are strongly affected by sex steroids in many songbird species, this system has become regarded as an ideal model system in which one can potentially determine how steroids affect neuronal anatomy, how altered anatomy leads to altered physiology, and how the altered physiology causes changes in singing. In the initial part of this review, I shall focus on canaries and zebra finches as most of our knowledge of the song system has been obtained from these two species. I shall describe singing behavior, the constituents of the song system, what is known of how these nuclei contribute to song, and how each is affected by steroid fluctuations. I shall then speculate on new ways of posing questions on hormone--anatomy interaction in this system (which I will illustrate with preliminary data from my own lab). This review will be brief as several reviews of aspects of the song system have recently been published (Arnold, 1982; Nottebohm, 1984; Arnold and Gorski, 1984; DeVoogd, 1984; Konishi, 1985).
继诺特博姆的开创性工作之后,鸣禽中参与歌曲产生的脑区已成为多个实验室广泛研究的焦点。在许多鸣禽物种中,由于歌唱行为和歌曲控制区域的神经解剖结构都受到性类固醇的强烈影响,这个系统已被视为一个理想的模型系统,在其中人们有可能确定类固醇如何影响神经元解剖结构,解剖结构的改变如何导致生理变化,以及生理变化如何引起歌唱的改变。在本综述的第一部分,我将重点讨论金丝雀和斑胸草雀,因为我们对歌曲系统的大部分了解都来自这两个物种。我将描述歌唱行为、歌曲系统的组成部分、这些核团如何对歌曲产生作用的已知情况,以及每个核团如何受到类固醇波动的影响。然后,我将推测在这个系统中提出关于激素与解剖结构相互作用问题的新方法(我将用我自己实验室的初步数据进行说明)。由于最近已经发表了几篇关于歌曲系统各方面的综述(阿诺德,1982年;诺特博姆,1984年;阿诺德和戈尔斯基,1984年;德沃格德,1984年;小西,1985年),所以本综述将较为简短。