Effect of nitric oxide on single skeletal muscle fibres from the mouse

被引:110
作者
Andrade, FH
Reid, MB
Allen, DG
Westerblad, H [1 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
[2] Univ Kentucky, Med Ctr, Dept Anat & Neurobiol, Lexington, KY 40536 USA
[3] Baylor Coll Med, Pulm & Crit Care Med Sect, Houston, TX 77030 USA
[4] Univ Sydney, Dept Physiol, Sydney, NSW 2006, Australia
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1998年 / 509卷 / 02期
关键词
D O I
10.1111/j.1469-7793.1998.577bn.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. Single skeletal muscle fibres from a mouse foot muscle were used to investigate the effects of nitric oxide on contractile function. 2. We measured force production and myoplasmic free Ca2+ concentration ([Ca2+](i)) in single fibres exposed to the nitric oxide donors S-nitroso-N-acetylcysteine (SNAC) and nitroprusside. 3. The nitric oxide donors reduced myofibrillar Ca2+ sensitivity whereas [Ca2+](i) transients were increased during submaximal tetani. Force was largely unchanged. SNAC did not change maximum shortening velocity, the rate of force redevelopment, or force production at saturating [Ca2+](i). 4. The guanylyl cyclase inhibitor LY83583 increased tetanic [Ca2+](i) but had no effect on Ca2+ sensitivity. LY83583 did not prevent the decrease in myofibrillar Ca2+ sensitivity in response to SNAC. The oxidizer sodium nitrite increased tetanic [Ca2+](i) and decreased myofibrillar Ca2+ sensitivity. 5. We conclude that under our experimental conditions nitric oxide impairs Ca2+ activation of the actin filaments which results in decreased myofibrillar Ca2+ sensitivity.
引用
收藏
页码:577 / 586
页数:10
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