Evolutionary scaling and cognitive correlates of primate frontal cortex microstructure.

IF 2.7 3区 医学 Q1 ANATOMY & MORPHOLOGY Brain Structure & Function Pub Date : 2024-11-01 Epub Date: 2023-10-27 DOI:10.1007/s00429-023-02719-7
Cheryl D Stimpson, Jeroen B Smaers, Mary Ann Raghanti, Kimberley A Phillips, Bob Jacobs, William D Hopkins, Patrick R Hof, Chet C Sherwood
{"title":"Evolutionary scaling and cognitive correlates of primate frontal cortex microstructure.","authors":"Cheryl D Stimpson, Jeroen B Smaers, Mary Ann Raghanti, Kimberley A Phillips, Bob Jacobs, William D Hopkins, Patrick R Hof, Chet C Sherwood","doi":"10.1007/s00429-023-02719-7","DOIUrl":null,"url":null,"abstract":"<p><p>Investigating evolutionary changes in frontal cortex microstructure is crucial to understanding how modifications of neuron and axon distributions contribute to phylogenetic variation in cognition. In the present study, we characterized microstructural components of dorsolateral prefrontal cortex, orbitofrontal cortex, and primary motor cortex from 14 primate species using measurements of neuropil fraction and immunohistochemical markers for fast-spiking inhibitory interneurons, large pyramidal projection neuron subtypes, serotonergic innervation, and dopaminergic innervation. Results revealed that the rate of evolutionary change was similar across these microstructural variables, except for neuropil fraction, which evolves more slowly and displays the strongest correlation with brain size. We also found that neuropil fraction in orbitofrontal cortex layers V-VI was associated with cross-species variation in performance on experimental tasks that measure self-control. These findings provide insight into the evolutionary reorganization of the primate frontal cortex in relation to brain size scaling and its association with cognitive processes.</p>","PeriodicalId":9145,"journal":{"name":"Brain Structure & Function","volume":" ","pages":"1823-1838"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Structure & Function","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00429-023-02719-7","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ANATOMY & MORPHOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Investigating evolutionary changes in frontal cortex microstructure is crucial to understanding how modifications of neuron and axon distributions contribute to phylogenetic variation in cognition. In the present study, we characterized microstructural components of dorsolateral prefrontal cortex, orbitofrontal cortex, and primary motor cortex from 14 primate species using measurements of neuropil fraction and immunohistochemical markers for fast-spiking inhibitory interneurons, large pyramidal projection neuron subtypes, serotonergic innervation, and dopaminergic innervation. Results revealed that the rate of evolutionary change was similar across these microstructural variables, except for neuropil fraction, which evolves more slowly and displays the strongest correlation with brain size. We also found that neuropil fraction in orbitofrontal cortex layers V-VI was associated with cross-species variation in performance on experimental tasks that measure self-control. These findings provide insight into the evolutionary reorganization of the primate frontal cortex in relation to brain size scaling and its association with cognitive processes.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
灵长类动物额叶皮层微观结构的进化尺度和认知相关性。
研究额叶皮层微观结构的进化变化对于理解神经元和轴突分布的改变如何促进认知系统发育变化至关重要。在本研究中,我们使用神经胶质分数和快速尖峰抑制性中间神经元、大锥体投射神经元亚型、5-羟色胺能神经支配和多巴胺能神经支配的免疫组织化学标记物,对14种灵长类动物的背外侧前额叶皮层、眶额皮层和初级运动皮层的微观结构成分进行了表征。结果显示,这些微观结构变量的进化变化率相似,除了神经纤毛部分,它进化得更慢,与大脑大小的相关性最强。我们还发现,眶额皮层V-VI层的神经胶质分数与测量自我控制的实验任务表现的跨物种差异有关。这些发现深入了解了灵长类动物额叶皮层的进化重组与大脑大小缩放及其与认知过程的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Brain Structure & Function
Brain Structure & Function 医学-解剖学与形态学
CiteScore
6.00
自引率
6.50%
发文量
168
审稿时长
8 months
期刊介绍: Brain Structure & Function publishes research that provides insight into brain structure−function relationships. Studies published here integrate data spanning from molecular, cellular, developmental, and systems architecture to the neuroanatomy of behavior and cognitive functions. Manuscripts with focus on the spinal cord or the peripheral nervous system are not accepted for publication. Manuscripts with focus on diseases, animal models of diseases, or disease-related mechanisms are only considered for publication, if the findings provide novel insight into the organization and mechanisms of normal brain structure and function.
期刊最新文献
Redefining language networks: connectivity beyond localised regions. Retraction Note: Developmental changes in Notch1 and NLE1 expression in a genetic model of absence epilepsy. Correction: Histamine induces the production of matrix metalloproteinase-9 in human astrocytic cultures via H1-receptor subtype. Towards multi-modal, multi-species brain atlases: part two. A new map of the rat isocortex and proisocortex: cytoarchitecture and M2 receptor distribution patterns.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1