Resistance Training, Recovery and Genetics: AMPD1 the Gene for Recovery

C. Collins
{"title":"Resistance Training, Recovery and Genetics: AMPD1 the Gene for Recovery","authors":"C. Collins","doi":"10.4172/2324-9080.1000256","DOIUrl":null,"url":null,"abstract":"Genetics play a major role in every aspect of our lives; they determine our hair colour, eye colour, height, disease risks, gifts and some of our mannerisms. As such they also play a large function in our response to exercise and physical stressors. The gene AMPD1 is a protein coding gene, encoding adenosine monophosphate deminase 1. AMPD1 catalyses the deamination (the removal of an amine group from a molecule) of AMP to IMP in skeletal muscle, deficiency of the AMPD1 enzyme is a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy. It appears that those with at least one T variant in AMPD1 (rs17602729) require longer rest periods between bouts of weight training, require longer between sessions and have increased perceived pain post training.","PeriodicalId":90574,"journal":{"name":"Journal of athletic enhancement","volume":"2000 1","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2017-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of athletic enhancement","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2324-9080.1000256","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8

Abstract

Genetics play a major role in every aspect of our lives; they determine our hair colour, eye colour, height, disease risks, gifts and some of our mannerisms. As such they also play a large function in our response to exercise and physical stressors. The gene AMPD1 is a protein coding gene, encoding adenosine monophosphate deminase 1. AMPD1 catalyses the deamination (the removal of an amine group from a molecule) of AMP to IMP in skeletal muscle, deficiency of the AMPD1 enzyme is a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy. It appears that those with at least one T variant in AMPD1 (rs17602729) require longer rest periods between bouts of weight training, require longer between sessions and have increased perceived pain post training.
抗阻训练,恢复和遗传学:AMPD1 -恢复基因
基因在我们生活的方方面面都扮演着重要的角色;它们决定了我们的头发颜色、眼睛颜色、身高、患病风险、天赋和一些习惯。因此,它们在我们对运动和身体压力的反应中也起着很大的作用。基因AMPD1是一个蛋白质编码基因,编码单磷酸腺苷脱胺酶1。AMPD1在骨骼肌中催化AMP脱胺(从分子中去除胺基)到IMP,缺乏AMPD1酶是运动诱导肌病的常见原因,可能是代谢性肌病的最常见原因。那些AMPD1 (rs17602729)中至少有一个T变异的人,在举重训练之间需要更长的休息时间,训练之间需要更长的休息时间,训练后的疼痛感也会增加。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信
小红书