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疲劳和氧化对完整肌纤维和从小鼠膈肌分离的肌原纤维收缩功能的影响。

The effects of fatigue and oxidation on contractile function of intact muscle fibers and myofibrils isolated from the mouse diaphragm.

机构信息

Dept Experimental and Clinical Medicine, University of Firenze, Florence, Italy.

Dept Kinesiology and Physical Education, Faculty of Education, McGill University, Montreal, Canada.

出版信息

Sci Rep. 2019 Mar 14;9(1):4422. doi: 10.1038/s41598-019-39353-5.

Abstract

The goal of this study was to investigate the effects of repetitive stimulation and the oxidant HO on fatigue of diaphragm intact fibers and in myofibrils measured with different Ca concentrations. Intact fibers were isolated from mice diaphragm, and twitch and tetanic contractions (500 ms duration) were performed at different frequencies of stimulation ranging from 15 Hz to 150 Hz to establish a force-frequency relation before and after a fatigue and recovery protocol, without or after a treatment with HO. Fatigue was induced with isometric contractions (500 ms, 40 Hz) evoked every 0.8 seconds, with a total of 625 tetani. After the fatigue, the force recovery was followed by invoking tetanic contractions (500 ms, 40 Hz) every 1 min, with a total duration of 30 min. Individual myofibrils were also isolated from the mouse diaphragm and were tested for isometric contractions before and after treatment with HO and NAC. In a second series of experiments, myofibrils were activated at different pCa (pCa = -log [Ca]), before and after HO treatment. After 15 minutes of HO treatment, the myofibrillar force was decreased to 54 ± 12% of its control, maximal value, and a result that was reversed by NAC treatment. The force was also decreased after myofibrils were treated with HO and activated in pCa ranging between 4.5 and 5.7. These results suggest that fatigue in diaphragm intact fibers and at the myofibrils level is caused partially by oxidation of the contractile proteins that may be responsible for changing the force in various levels of Ca activation.

摘要

本研究旨在探讨重复刺激和氧化剂 HO 对完整纤维和不同 Ca 浓度下肌原纤维疲劳的影响。从小鼠膈肌中分离出完整纤维,在 15 Hz 至 150 Hz 的不同刺激频率下进行单次收缩和强直收缩(500 ms 时程),以建立力-频率关系,然后在疲劳和恢复方案前后进行,不进行或进行 HO 处理。通过等长收缩(500 ms,40 Hz)进行疲劳诱导,每 0.8 秒收缩一次,总共进行 625 次收缩。疲劳后,通过每隔 1 分钟进行一次强直收缩(500 ms,40 Hz)来跟踪力的恢复,总共持续 30 分钟。还从小鼠膈肌中分离出单个肌原纤维,并在 HO 和 NAC 处理前后进行等长收缩测试。在第二系列实验中,在 HO 处理前后,用不同的 pCa(pCa = -log [Ca])激活肌原纤维。HO 处理 15 分钟后,肌原纤维的力降低至其对照的 54±12%,最大值,这一结果通过 NAC 处理得到逆转。当肌原纤维在 pCa 范围为 4.5 和 5.7 之间被 HO 处理并激活时,力也会降低。这些结果表明,膈肌完整纤维和肌原纤维水平的疲劳部分是由收缩蛋白的氧化引起的,这可能是导致不同 Ca 激活水平下力变化的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99c2/6418105/c60697c6cf97/41598_2019_39353_Fig1_HTML.jpg

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