Intrinsic motoneuron properties in typical human development

Author:

Mohammadalinejad Ghazaleh123ORCID,Afsharipour Babak123ORCID,Yacyshyn Alex12ORCID,Duchcherer Jennifer12,Bashuk Jack12,Bennett Erin12ORCID,Pearcey Gregory E. P.4ORCID,Negro Francesco5ORCID,Quinlan Katharina A.6ORCID,Bennett David J.27ORCID,Gorassini Monica A.123ORCID

Affiliation:

1. Department of Medicine, Faculty of Medicine and Dentistry University of Alberta Edmonton AB Canada

2. Neuroscience and Mental Health Institute University of Alberta Edmonton AB Canada

3. Women and Children's Health Research Institute University of Alberta Edmonton AB Canada

4. School of Human Kinetics and Recreation, Memorial University of Newfoundland, St John's Canada and Physical Therapy & Human Movement Sciences Northwestern University Chicago IL USA

5. Clinical and Experimental Sciences Universita degli Studi di Brescia Brescia Italia

6. George and Anne Ryan Institute for Neuroscience, Biomedical and Pharmaceutical Sciences, College of Pharmacy University of Rhode Island Kingston RI USA

7. Faculty of Rehabilitation Medicine University of Alberta Edmonton AB Canada

Abstract

AbstractMotoneuron properties and their firing patterns undergo significant changes throughout development and in response to neuromodulators such as serotonin. Here, we examined the age‐related development of self‐sustained firing and general excitability of tibialis anterior motoneurons in a young development (7–17 years), young adult (18–28 years) and adult (32–53 years) group, as well as in a separate group of participants taking selective serotonin reuptake inhibitors (SSRIs, aged 11–28 years). Self‐sustained firing, as measured by ΔF, was larger in the young development (∼5.8 Hz, n = 20) compared to the young adult (∼4.9 Hz, n = 13) and adult (∼4.8 Hz, n = 8) groups, consistent with a developmental decrease in self‐sustained firing mediated by persistent inward currents (PIC). ΔF was also larger in participants taking SSRIs (∼6.5 Hz, n = 9) compared to their age‐matched controls (∼5.3 Hz, n = 26), consistent with increased levels of spinal serotonin facilitating the motoneuron PIC. Participants in the young development and SSRI groups also had higher firing rates and a steeper acceleration in initial firing rates (secondary ranges), consistent with the PIC producing a steeper acceleration in membrane depolarization at the onset of motoneuron firing. In summary, both the young development and SSRI groups exhibited increased intrinsic motoneuron excitability compared to the adults, which, in the young development group, was also associated with a larger unsteadiness in the dorsiflexion torque profiles. We propose several intrinsic and extrinsic factors that affect both motoneuron PICs and cell discharge which vary during development, with a time course similar to the changes in motoneuron firing behaviour observed in the present study. imageKey points Neurons in the spinal cord that activate muscles in the limbs (motoneurons) undergo increases in excitability shortly after birth to help animals stand and walk. We examined whether the excitability of human ankle flexor motoneurons also continues to change from child to adulthood by recording the activity of the muscle fibres they innervate. Motoneurons in children and adolescents aged 7–17 years (young development group) had higher signatures of excitability that included faster firing rates and more self‐sustained activity compared to adults aged ≥18 years. Participants aged 11–28 years of age taking serotonin reuptake inhibitors had the highest measures of motoneuron excitability compared to their age‐matched controls. The young development group also had more unstable contractions, which might partly be related to the high excitability of the motoneurons.

Funder

Natural Sciences and Engineering Research Council of Canada

Women and Children's Health Research Institute

Publisher

Wiley

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3