利用解剖和切片技术对埃及果蝠(Rousettus aegyptiacus)翅膀肌肉进行功能解剖。

IF 1.8 3区 医学 Q2 ANATOMY & MORPHOLOGY
Roger W P Kissane, Amy Griffiths, Alana C Sharp
{"title":"利用解剖和切片技术对埃及果蝠(Rousettus aegyptiacus)翅膀肌肉进行功能解剖。","authors":"Roger W P Kissane, Amy Griffiths, Alana C Sharp","doi":"10.1111/joa.14145","DOIUrl":null,"url":null,"abstract":"<p><p>Bats are unique among mammals for evolving powered flight. However, very little data are available on the muscle properties and architecture of bat flight muscles. Diffusible iodine contrast-enhanced computed tomography (diceCT) is an established tool for 3D visualisation of anatomy and is becoming a more readily accessible and widely used technique. Here, we combine this technique with gross dissection of the Egyptian fruit bat (Rousettus aegyptiacus) to compare muscle masses, fibre lengths and physiological cross-sectional areas (PCSA) of muscles with published forelimb data from an array of non-flying mammals and flying birds. The Egyptian fruit bat has a highly specialised pectoralis (pars posterior) architecturally optimised to generate power. The elbow flexion/extension muscles (biceps brachii and triceps brachii) have comparable PCSAs to the pectoralis, but shorter fibre lengths, which are optimised to generate large forces. Our data also show that the Egyptian fruit bat is more similar to flying birds than non-flying mammals with its highly disparate muscle architecture. Specifically, the Egyptian fruit bat have uniquely enlarged pectoralis muscles and elbow flexion and extension muscles (bicep brachii and triceps brachii) to aid powered flight. Finally, while the Egyptian fruit bat has a comparable heterogeneity in pectoralis (pars posterior) fibre length across the cranial-caudal axis to that seen in birds, the average normalised fibre length is larger than that seen in any of the surveyed birds. Our data here provide a greater understanding of the anatomy and functional specialisation of the forelimb musculature that powers flight.</p>","PeriodicalId":14971,"journal":{"name":"Journal of Anatomy","volume":" ","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Functional anatomy of the wing muscles of the Egyptian fruit bat (Rousettus aegyptiacus) using dissection and diceCT.\",\"authors\":\"Roger W P Kissane, Amy Griffiths, Alana C Sharp\",\"doi\":\"10.1111/joa.14145\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bats are unique among mammals for evolving powered flight. However, very little data are available on the muscle properties and architecture of bat flight muscles. Diffusible iodine contrast-enhanced computed tomography (diceCT) is an established tool for 3D visualisation of anatomy and is becoming a more readily accessible and widely used technique. Here, we combine this technique with gross dissection of the Egyptian fruit bat (Rousettus aegyptiacus) to compare muscle masses, fibre lengths and physiological cross-sectional areas (PCSA) of muscles with published forelimb data from an array of non-flying mammals and flying birds. The Egyptian fruit bat has a highly specialised pectoralis (pars posterior) architecturally optimised to generate power. The elbow flexion/extension muscles (biceps brachii and triceps brachii) have comparable PCSAs to the pectoralis, but shorter fibre lengths, which are optimised to generate large forces. Our data also show that the Egyptian fruit bat is more similar to flying birds than non-flying mammals with its highly disparate muscle architecture. Specifically, the Egyptian fruit bat have uniquely enlarged pectoralis muscles and elbow flexion and extension muscles (bicep brachii and triceps brachii) to aid powered flight. Finally, while the Egyptian fruit bat has a comparable heterogeneity in pectoralis (pars posterior) fibre length across the cranial-caudal axis to that seen in birds, the average normalised fibre length is larger than that seen in any of the surveyed birds. Our data here provide a greater understanding of the anatomy and functional specialisation of the forelimb musculature that powers flight.</p>\",\"PeriodicalId\":14971,\"journal\":{\"name\":\"Journal of Anatomy\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2024-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Anatomy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/joa.14145\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ANATOMY & MORPHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Anatomy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/joa.14145","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ANATOMY & MORPHOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

蝙蝠是哺乳动物中唯一进化出动力飞行的动物。然而,有关蝙蝠飞行肌肉特性和结构的数据却很少。可扩散碘对比增强计算机断层扫描(骰CT)是一种用于解剖学三维可视化的成熟工具,正在成为一种更容易获得和广泛使用的技术。在这里,我们将这一技术与埃及果蝠(Rousettus aegyptiacus)的大体解剖相结合,将肌肉质量、纤维长度和肌肉生理横截面积(PCSA)与已发表的一系列非飞行哺乳动物和飞行鸟类的前肢数据进行比较。埃及果蝠的胸肌(后副肌)高度特化,其结构经过优化,能够产生力量。肘部屈/伸肌(肱二头肌和肱三头肌)的 PCSA 与胸肌相当,但纤维长度较短,可产生较大的力量。我们的数据还显示,埃及果蝠的肌肉结构与非飞行哺乳动物相比,更类似于飞行鸟类。具体来说,埃及果蝠的胸肌和肘部屈伸肌(肱二头肌和肱三头肌)独特地增大,有助于动力飞行。最后,虽然埃及果蝠的胸肌(后副肌)纤维长度在头颅-尾轴的异质性与鸟类相当,但其平均归一化纤维长度大于任何一种调查鸟类。我们在此获得的数据使我们对前肢肌肉组织的解剖结构和功能特化有了更深入的了解,这些肌肉组织为飞行提供了动力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional anatomy of the wing muscles of the Egyptian fruit bat (Rousettus aegyptiacus) using dissection and diceCT.

Bats are unique among mammals for evolving powered flight. However, very little data are available on the muscle properties and architecture of bat flight muscles. Diffusible iodine contrast-enhanced computed tomography (diceCT) is an established tool for 3D visualisation of anatomy and is becoming a more readily accessible and widely used technique. Here, we combine this technique with gross dissection of the Egyptian fruit bat (Rousettus aegyptiacus) to compare muscle masses, fibre lengths and physiological cross-sectional areas (PCSA) of muscles with published forelimb data from an array of non-flying mammals and flying birds. The Egyptian fruit bat has a highly specialised pectoralis (pars posterior) architecturally optimised to generate power. The elbow flexion/extension muscles (biceps brachii and triceps brachii) have comparable PCSAs to the pectoralis, but shorter fibre lengths, which are optimised to generate large forces. Our data also show that the Egyptian fruit bat is more similar to flying birds than non-flying mammals with its highly disparate muscle architecture. Specifically, the Egyptian fruit bat have uniquely enlarged pectoralis muscles and elbow flexion and extension muscles (bicep brachii and triceps brachii) to aid powered flight. Finally, while the Egyptian fruit bat has a comparable heterogeneity in pectoralis (pars posterior) fibre length across the cranial-caudal axis to that seen in birds, the average normalised fibre length is larger than that seen in any of the surveyed birds. Our data here provide a greater understanding of the anatomy and functional specialisation of the forelimb musculature that powers flight.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Anatomy
Journal of Anatomy 医学-解剖学与形态学
CiteScore
4.80
自引率
8.30%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Journal of Anatomy is an international peer-reviewed journal sponsored by the Anatomical Society. The journal publishes original papers, invited review articles and book reviews. Its main focus is to understand anatomy through an analysis of structure, function, development and evolution. Priority will be given to studies of that clearly articulate their relevance to the anatomical community. Focal areas include: experimental studies, contributions based on molecular and cell biology and on the application of modern imaging techniques and papers with novel methods or synthetic perspective on an anatomical system. Studies that are essentially descriptive anatomy are appropriate only if they communicate clearly a broader functional or evolutionary significance. You must clearly state the broader implications of your work in the abstract. We particularly welcome submissions in the following areas: Cell biology and tissue architecture Comparative functional morphology Developmental biology Evolutionary developmental biology Evolutionary morphology Functional human anatomy Integrative vertebrate paleontology Methodological innovations in anatomical research Musculoskeletal system Neuroanatomy and neurodegeneration Significant advances in anatomical education.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信