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Vacuole formation in fatigued skeletal muscle fibres from frog and mouse: effects of extracellular lactate

机译:青蛙和小鼠疲劳骨骼肌纤维中的液泡形成:细胞外乳酸的影响

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摘要

class="enumerated" style="list-style-type:decimal">Isolated, living muscle fibres from either Xenopus or mouse were observed in a confocal microscope and t-tubules were visualized with sulforhodamine B. Observations were made before and after fatiguing stimulation. In addition, experiments were performed on fibres observed in an ordinary light microscope with dark-field illumination.In Xenopus fibres, recovering after fatigue, t-tubules started to show dilatations 2-5 min post-fatigue. These swellings increased in size over the next 10-20 min to form vacuoles. After 2-3 h of recovery the appearance of the fibres was again normal and force production, which had been markedly depressed 10-40 min post-fatigue, was close to control. Vacuoles were not observed in mouse fibres, fatigued with the same protocol and allowed to recover.In Xenopus fibres, fatigued in normal Ringer solution and allowed to recover in Ringer solution with 30-50 mM L-lactate substituting for chloride (lactate-Ringer), the number and size of vacuoles were markedly reduced. Also, force recovery was significantly faster. Replacement of chloride by methyl sulphate or glucuronate had no effect on vacuolation.Resting Xenopus fibres exposed to 50 mm lactate-Ringer and transferred to normal Ringer solution displayed vacuoles within 5-10 min, but to a smaller extent than after fatigue. Vacuolation was not associated with marked force reduction.Mouse fibres, fatigued in 50 mm lactate-Tyrode (l-lactate substituting for chloride in Tyrode solution) and recovering in normal Tyrode solution, displayed vacuoles for a limited period post-fatigue. Vacuolation had no effect on force production.The results are consistent with the view that lactate, formed during fatigue, is transported into the t-tubules where it attracts water and causes t-tubule swelling and vacuolation. This vacuolation may be counteracted in vivo due to a gradual extracellular accumulation of lactate during fatigue.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在共聚焦显微镜下观察到来自非洲爪蟾或小鼠的分离的活肌纤维,并用磺基罗丹明B观察T管。在刺激疲劳之前和之后进行观察。此外,还对用普通光学显微镜在暗场照明下观察到的纤维进行了实验。 在非洲爪蟾的纤维中,疲劳后恢复,t形小管在疲劳后2-5分钟开始显示出膨胀。这些肿胀在接下来的10-20分钟内增大,形成液泡。恢复2-3小时后,纤维的外观再次恢复正常,并且在疲劳后10-40分钟显着降低的力产生接近于对照。在小鼠纤维中未观察到液泡,经相同实验方案疲劳并恢复。 在非洲爪蟾纤维中,在正常林格溶液中疲劳并在林格溶液中用30-50 mM L-乳酸替代恢复。对于氯化物(乳酸-林格),液泡的数量和大小显着减少。同样,力量恢复明显更快。硫酸甲酯或葡糖醛酸酯代替氯化物对空泡没有影响。 将非洲爪蟾的纤维暴露于50 mm乳酸-林格氏液中并转移到正常的林格溶液中,在5-10分钟内显示出空泡,但程度较小比疲劳后。抽空与明显的力降低无关。 小鼠纤维,在50 mm乳酸-Tyrode(L-乳酸替代蒂罗德溶液中的氯化物)中疲劳,在正常的蒂罗德溶液中恢复,在有限的时间内显示出液泡疲劳后。抽气对力的产生没有影响。 结果与以下观点一致:在疲劳过程中形成的乳酸被转运到T形小管中,在那里它吸水并导致T形管肿胀和空泡化。这种空泡作用可能在体内被抵消,这是由于疲劳期间乳酸逐渐在细胞外积聚。

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