Sandra J. Niederschuh, Julia van Beesel , Manuela Schmidt
{"title":"腕窦毛的感觉反馈在大鼠(Rattus norvegicus, Rodentia)在狭窄基质上行走时运动运动学中的作用","authors":"Sandra J. Niederschuh, Julia van Beesel , Manuela Schmidt","doi":"10.1016/j.zool.2022.126055","DOIUrl":null,"url":null,"abstract":"<div><p><span>Carpal sinus hairs on the forearms are assumed to have evolved within the stem lineage of Theria<span>. The presence and similar position of these specialized tactile hairs in scansorial and terrestrial species<span> as well as earlier studies on rats indicate a biological role in sensing substrate irregularities in high structured environments to ensure the dynamic stability of the body during locomotion. While these sensors were considered as one functional unit until so far, the present study deals with the biological role of the single tactile hairs of the trident, assuming a role in sensing substrate diameters and adapting limb coordination and body posture to different arboreal inclinations. To investigate the influence of each hair, we studied the locomotion of rats on poles of two different diameters whereby we selectively removed individual carpal sinus hairs. The rats walked at speeds ranging from 0.12 m/s to 0.58 m/s. Normal-light high-speed cameras and x-ray fluoroscopy visualized the hairs and body dynamics during locomotion. The time lag between first contact of the hairs to the branch until contact of the forepaw was 56–108 ms. Within this time window the pronation/supination of the paw and anterior body posture are adjusted to the substrate diameter. We presume that the most proximal sinus hair (located between the medial and lateral one) senses the paw-substrate distance through the increasing bend from its first branch-contact until the contact of the paw. The medial and the lateral hairs touch the pole sides and thereby, may collect information about the properties of the small-diameter substrate. The removal of single hairs from the group results in minor changes of kinematic parameters, but locomotor stability is seriously impaired when more than one hair is cut. The kinematic responses span from a more crouched body posture and higher forearm </span></span></span>pronation to paw slipping, muscle tremor or complete refusal to walk on the narrow substrate.</p></div>","PeriodicalId":49330,"journal":{"name":"Zoology","volume":"155 ","pages":"Article 126055"},"PeriodicalIF":1.6000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"The role of sensory feedback from carpal sinus hairs in locomotor kinematics of rats (Rattus norvegicus, Rodentia) during walking on narrow substrates\",\"authors\":\"Sandra J. Niederschuh, Julia van Beesel , Manuela Schmidt\",\"doi\":\"10.1016/j.zool.2022.126055\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Carpal sinus hairs on the forearms are assumed to have evolved within the stem lineage of Theria<span>. The presence and similar position of these specialized tactile hairs in scansorial and terrestrial species<span> as well as earlier studies on rats indicate a biological role in sensing substrate irregularities in high structured environments to ensure the dynamic stability of the body during locomotion. While these sensors were considered as one functional unit until so far, the present study deals with the biological role of the single tactile hairs of the trident, assuming a role in sensing substrate diameters and adapting limb coordination and body posture to different arboreal inclinations. To investigate the influence of each hair, we studied the locomotion of rats on poles of two different diameters whereby we selectively removed individual carpal sinus hairs. The rats walked at speeds ranging from 0.12 m/s to 0.58 m/s. Normal-light high-speed cameras and x-ray fluoroscopy visualized the hairs and body dynamics during locomotion. The time lag between first contact of the hairs to the branch until contact of the forepaw was 56–108 ms. Within this time window the pronation/supination of the paw and anterior body posture are adjusted to the substrate diameter. We presume that the most proximal sinus hair (located between the medial and lateral one) senses the paw-substrate distance through the increasing bend from its first branch-contact until the contact of the paw. The medial and the lateral hairs touch the pole sides and thereby, may collect information about the properties of the small-diameter substrate. The removal of single hairs from the group results in minor changes of kinematic parameters, but locomotor stability is seriously impaired when more than one hair is cut. The kinematic responses span from a more crouched body posture and higher forearm </span></span></span>pronation to paw slipping, muscle tremor or complete refusal to walk on the narrow substrate.</p></div>\",\"PeriodicalId\":49330,\"journal\":{\"name\":\"Zoology\",\"volume\":\"155 \",\"pages\":\"Article 126055\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zoology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0944200622000563\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ZOOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zoology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0944200622000563","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ZOOLOGY","Score":null,"Total":0}
The role of sensory feedback from carpal sinus hairs in locomotor kinematics of rats (Rattus norvegicus, Rodentia) during walking on narrow substrates
Carpal sinus hairs on the forearms are assumed to have evolved within the stem lineage of Theria. The presence and similar position of these specialized tactile hairs in scansorial and terrestrial species as well as earlier studies on rats indicate a biological role in sensing substrate irregularities in high structured environments to ensure the dynamic stability of the body during locomotion. While these sensors were considered as one functional unit until so far, the present study deals with the biological role of the single tactile hairs of the trident, assuming a role in sensing substrate diameters and adapting limb coordination and body posture to different arboreal inclinations. To investigate the influence of each hair, we studied the locomotion of rats on poles of two different diameters whereby we selectively removed individual carpal sinus hairs. The rats walked at speeds ranging from 0.12 m/s to 0.58 m/s. Normal-light high-speed cameras and x-ray fluoroscopy visualized the hairs and body dynamics during locomotion. The time lag between first contact of the hairs to the branch until contact of the forepaw was 56–108 ms. Within this time window the pronation/supination of the paw and anterior body posture are adjusted to the substrate diameter. We presume that the most proximal sinus hair (located between the medial and lateral one) senses the paw-substrate distance through the increasing bend from its first branch-contact until the contact of the paw. The medial and the lateral hairs touch the pole sides and thereby, may collect information about the properties of the small-diameter substrate. The removal of single hairs from the group results in minor changes of kinematic parameters, but locomotor stability is seriously impaired when more than one hair is cut. The kinematic responses span from a more crouched body posture and higher forearm pronation to paw slipping, muscle tremor or complete refusal to walk on the narrow substrate.
期刊介绍:
Zoology is a journal devoted to experimental and comparative animal science. It presents a common forum for all scientists who take an explicitly organism oriented and integrative approach to the study of animal form, function, development and evolution.
The journal invites papers that take a comparative or experimental approach to behavior and neurobiology, functional morphology, evolution and development, ecological physiology, and cell biology. Due to the increasing realization that animals exist only within a partnership with symbionts, Zoology encourages submissions of papers focused on the analysis of holobionts or metaorganisms as associations of the macroscopic host in synergistic interdependence with numerous microbial and eukaryotic species.
The editors and the editorial board are committed to presenting science at its best. The editorial team is regularly adjusting editorial practice to the ever changing field of animal biology.