Contractile function in vitro of slow-twitch skeletal muscle from weanling mice subjected to wasting malnutrition

Author:

Fischer J W,Reading S A,Hillyer L,Woodward B,Barclay J K

Abstract

Our hypothesis was that malnutrition sufficient to produce weight loss in weanling mice would decrease the ability of slow-twitch skeletal muscle to develop and maintain force. We isolated muscles from 3 groups (n = 5) of weanling C57BL/6J mice of both sexes (i) mice at 19 days of age serving as zero-time or baseline controls (CONT) (ii) mice fed for the next 14 days with a low-protein diet that produces features of incipient kwashiorkor (LPD) and (iii) mice fed for the next 14 days with a complete diet (NORM). Muscles were also obtained from 5 adult mice 7–9 months of age (MAT). We stimulated the soleus at 50 Hz for 500 ms at 0.6 tetanic contractions per min (tet·min–1), 6 tet·min–1, and 30 tet·min–1in Krebs-Henseleit bicarbonate buffer at 27°C gassed with 95% O2and 5% CO2. The initial developed force (mN·mm–2) at 0.6 tet·min–1did not differ across groups (CONT 211.7 ± 16.0, LPD 274.2 ± 41.6, NORM 246.8 ± 38.0, MAT 210.8 ± 10.6). The fatigue rate (mN·mm–2·min–1) at 6 tet·min–1was significantly slower in muscles from CONT (0.6 ± 0.3) and LPD (0.6 ± 0.4) than in NORM (2.4 ± 0.6) and MAT (2.3 ± 0.2). At 30 tet·min–1, the fatigue rate (mN·mm–2·min–1) did not differ across groups (CONT 2.4 ± 0.5, LPD 2.7 ± 0.5, NORM 2.5 ± 0.4, MAT 2.0 ± 0.2). After stimulation at 6 tet· min–1and 30 tet·min–1, only muscles from CONT and LPD recovered to 100%. Because muscles from LPD mice developed equal force, fatigued less, and recovered from fatigue to a greater extent than muscles from NORM mice, we rejected the hypothesis. The function of the tissue remaining in the muscles from LPD mice approximated that of muscles from mice at 19 days of age rather than muscles from either mice of the same age fed a complete diet or adult mice.Key words: developed force, fatigue, recovery from fatigue.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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