Abstract:The Bengalese finch was domesticated more than 250 years ago from the wild whiterumped munia (WRM). Similar to other domesticated species, Bengalese finches show a reduced fear response and have lower corticosterone levels, compared to WRMs.Bengalese finches and munias also have different song types. Since oxytocin (OT) has been found to be involved in stress coping and auditory processing, we tested whether the OT sequence and brain expression pattern and content differ in wild munias and domesticated Bengale… Show more
“…BF is a domesticated strain of the wild ancestor WRM, and a growing body of research suggests that in the course of the domestication process, BFs have acquired behavioral, anatomical, and neuroendocrine changes, including reduced sensitivity to environmental stresses ( Suzuki et al, 2014 ; Suzuki et al, 2021 ; Suzuki and Okanoya, 2021 ; Tobari et al, 2022 ). In particular, BFs exhibit reduced levels of fearfulness related to coping with predation ( Suzuki et al, 2013 ) and lower fecal CORT levels than WRM ( Suzuki et al, 2012 ).…”
The zebra finch (ZF) and the Bengalese finch (BF) are animal models that have been commonly used for neurobiological studies on vocal learning. Although they largely share the brain structure for vocal learning and production, BFs produce more complex and variable songs than ZFs, providing a great opportunity for comparative studies to understand how animals learn and control complex motor behaviors. Here, we performed a comparative study between the two species by focusing on intrinsic motivation for non-courtship singing (“undirected singing”), which is critical for the development and maintenance of song structure. A previous study has demonstrated that ZFs dramatically increase intrinsic motivation for undirected singing when singing is temporarily suppressed by a dark environment. We found that the same procedure in BFs induced the enhancement of intrinsic singing motivation to much smaller degrees than that in ZFs. Moreover, unlike ZFs that rarely sing in dark conditions, substantial portion of BFs exhibited frequent singing in darkness, implying that such “dark singing” may attenuate the enhancement of intrinsic singing motivation during dark periods. In addition, measurements of blood corticosterone levels in dark and light conditions provided evidence that although BFs have lower stress levels than ZFs in dark conditions, such lower stress levels in BFs are not the major factor responsible for their frequent dark singing. Our findings highlight behavioral and physiological differences in spontaneous singing behaviors of BFs and ZFs and provide new insights into the interactions between singing motivation, ambient light, and environmental stress.
“…BF is a domesticated strain of the wild ancestor WRM, and a growing body of research suggests that in the course of the domestication process, BFs have acquired behavioral, anatomical, and neuroendocrine changes, including reduced sensitivity to environmental stresses ( Suzuki et al, 2014 ; Suzuki et al, 2021 ; Suzuki and Okanoya, 2021 ; Tobari et al, 2022 ). In particular, BFs exhibit reduced levels of fearfulness related to coping with predation ( Suzuki et al, 2013 ) and lower fecal CORT levels than WRM ( Suzuki et al, 2012 ).…”
The zebra finch (ZF) and the Bengalese finch (BF) are animal models that have been commonly used for neurobiological studies on vocal learning. Although they largely share the brain structure for vocal learning and production, BFs produce more complex and variable songs than ZFs, providing a great opportunity for comparative studies to understand how animals learn and control complex motor behaviors. Here, we performed a comparative study between the two species by focusing on intrinsic motivation for non-courtship singing (“undirected singing”), which is critical for the development and maintenance of song structure. A previous study has demonstrated that ZFs dramatically increase intrinsic motivation for undirected singing when singing is temporarily suppressed by a dark environment. We found that the same procedure in BFs induced the enhancement of intrinsic singing motivation to much smaller degrees than that in ZFs. Moreover, unlike ZFs that rarely sing in dark conditions, substantial portion of BFs exhibited frequent singing in darkness, implying that such “dark singing” may attenuate the enhancement of intrinsic singing motivation during dark periods. In addition, measurements of blood corticosterone levels in dark and light conditions provided evidence that although BFs have lower stress levels than ZFs in dark conditions, such lower stress levels in BFs are not the major factor responsible for their frequent dark singing. Our findings highlight behavioral and physiological differences in spontaneous singing behaviors of BFs and ZFs and provide new insights into the interactions between singing motivation, ambient light, and environmental stress.
“…The zebra finch exhibits OT mRNA in BNSTm, PVN, and SON, while Bengalese finches ( Lonchura striata var. domestica ) and white‐rumped munias ( Lonchura striata ) have OT mRNA in the SON, PVN, and lateral hypothalamus (Tobari et al., 2022; Vicario et al., 2017). Therefore, OT expression in these areas appears to be shared across avian taxa.…”
Section: Discussionmentioning
confidence: 99%
“…and white-rumped munias (Lonchura striata) have OT mRNA in the SON, PVN, and lateral hypothalamus (Tobari et al, 2022;Vicario et al, 2017).…”
Section: Conserved Distribution In Hypothalamic Nucleimentioning
confidence: 99%
“…Past immunohistochemical investigations of OT peptide expression in birds were performed utilizing antigens produced in laboratory and that are no longer available (Goossens et al., 1977). More recently, several studies have sequenced the OT gene and characterized the expression of OT mRNA in a limited number of brain regions in songbirds via in situ hybridization (Barth et al., 1997; Tobari et al., 2022; Vicario et al., 2017). The gene for OT has been included in the zebra finch atlas (Tobari et al., 2022; Vicario et al., 2017; Zebra Finch Expression Brain Atlas, n.d.).…”
Section: Introductionmentioning
confidence: 99%
“…More recently, several studies have sequenced the OT gene and characterized the expression of OT mRNA in a limited number of brain regions in songbirds via in situ hybridization (Barth et al., 1997; Tobari et al., 2022; Vicario et al., 2017). The gene for OT has been included in the zebra finch atlas (Tobari et al., 2022; Vicario et al., 2017; Zebra Finch Expression Brain Atlas, n.d.). However, these studies have not comprehensively mapped the distribution of the mRNA, and the levels of mRNA expression can differ from peptide abundance due to regulatory posttranscriptional processes.…”
The avian homologue of oxytocin (OT), formerly called mesotocin, influences social behaviors in songbirds and potentially song production. We sought to characterize the distribution of OT peptide in the brain of two songbird species: canaries (Serinus canaria) and zebra finches (Taeniopygia guttata). To visualize OT, we performed immunocytochemistry using an antibody previously shown to identify OT in avian species. In both canaries and zebra finches, dense OT‐ir perikarya were located in the paraventricular nucleus (PVN), preoptic area (POA), supraoptic nucleus (SON), and medial bed nucleus of the stria terminalis (BNSTm). We also observed morphologically distinct OT‐ir cells scattered throughout the mesopallium. OT‐ir fibers were observed in the PVN, ventral medial hypothalamus (VMH), periaqueductal gray (PAG), intercollicular nucleus (ICo), and ventral tegmental area (VTA). We also observed punctate OT‐ir fibers in the song control nucleus HVC. In both male and female canaries, OT‐ir fibers were present in the lateral septum (LS), but innervation was greater in males. We did not observe this sex difference in zebra finches. Much of the OT staining observed is consistent with general distributions within the vertebrate hypothalamus, indicating a possible conserved function. However, some extra‐hypothalamic distributions, such as perikarya in the mesopallium, may be specific to songbirds and play a role in song perception and production. The presence of OT‐ir fibers in HVC and song control nuclei projecting dopaminergic regions provides anatomical evidence in support of the idea that OT can influence singing behavior—either directly via HVC or indirectly via the PAG, VTA, or POA.
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