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肌醇三磷酸增强去表皮心肌和骨骼肌中的钙释放。

Inositol trisphosphate enhances calcium release in skinned cardiac and skeletal muscle.

作者信息

Nosek T M, Williams M F, Zeigler S T, Godt R E

出版信息

Am J Physiol. 1986 May;250(5 Pt 1):C807-11. doi: 10.1152/ajpcell.1986.250.5.C807.

DOI:10.1152/ajpcell.1986.250.5.C807
PMID:3085514
Abstract

Experiments from other laboratories suggest that inositol trisphosphate (InsP3) may be involved in the excitation-contraction coupling (ECC) process of cardiac and skeletal muscle. Our results support this hypothesis. Studying fiber bundles (less than 200-microns diameter) from guinea pig papillary muscles skinned with saponin and mechanically skinned single fibers from frog semitendinosus muscle, we find that calcium-induced force oscillations (observed in solutions containing low ethyleneglycol-bis(beta-aminoethylether)-N,N'-tetraacetic acid and pCa 7.0) are enhanced in magnitude and frequency by InsP3 at concentrations as low as 1 microM. InsP3 at 10 microM can often induce such oscillations in mechanically skinned frog skeletal muscle. In skinned cardiac fibers, InsP3 increases the magnitude of caffeine contractures at submaximal caffeine concentrations to a greater extent than at near-maximal caffeine concentrations. InsP3 (30 microM) has no effect on either the calcium sensitivity or maximal force generated by the contractile apparatus of skinned cardiac muscle. We conclude that InsP3 has no direct effect on the contractile machinery but that it can modulate ECC by enhancing the calcium-induced release of calcium from the sarcoplasmic reticulum, possibly from the same pool and through the same mechanism as caffeine.

摘要

其他实验室的实验表明,肌醇三磷酸(InsP3)可能参与心肌和骨骼肌的兴奋-收缩偶联(ECC)过程。我们的结果支持这一假设。通过研究用皂角苷去皮的豚鼠乳头肌纤维束(直径小于200微米)以及青蛙半腱肌的机械去皮单纤维,我们发现,在含有低浓度乙二醇双(β-氨基乙醚)-N,N'-四乙酸且pCa为7.0的溶液中观察到的钙诱导的力振荡,在低至1微摩尔浓度的InsP3作用下,其幅度和频率都会增强。10微摩尔浓度的InsP3常常能在机械去皮的青蛙骨骼肌中诱导出此类振荡。在去皮的心脏纤维中,InsP3在低于最大咖啡因浓度时比在接近最大咖啡因浓度时能更大程度地增加咖啡因挛缩的幅度。InsP3(30微摩尔)对去皮心肌收缩装置的钙敏感性或产生的最大力量均无影响。我们得出结论,InsP3对收缩机制没有直接影响,但它可以通过增强钙诱导的肌浆网钙释放来调节ECC,可能与咖啡因来自同一钙库并通过相同机制。

相似文献

1
Inositol trisphosphate enhances calcium release in skinned cardiac and skeletal muscle.肌醇三磷酸增强去表皮心肌和骨骼肌中的钙释放。
Am J Physiol. 1986 May;250(5 Pt 1):C807-11. doi: 10.1152/ajpcell.1986.250.5.C807.
2
An examination of the ability of inositol 1,4,5-trisphosphate to induce calcium release and tension development in skinned skeletal muscle fibres of frog and crustacea.对肌醇1,4,5 -三磷酸诱导青蛙和甲壳纲动物去表皮骨骼肌纤维中钙释放及张力产生能力的研究。
FEBS Lett. 1986 Oct 20;207(1):153-61. doi: 10.1016/0014-5793(86)80031-x.
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Inositol 1,4,5-trisphosphate-induced Ca2+ release from the sarcoplasmic reticulum and contraction in crustacean muscle.肌醇1,4,5 -三磷酸诱导的钙离子从肌浆网释放及甲壳类肌肉收缩
Can J Physiol Pharmacol. 1987 Apr;65(4):672-80. doi: 10.1139/y87-111.
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Inositol trisphosphate stimulates calcium release from peeled skeletal muscle fibers.肌醇三磷酸刺激去膜骨骼肌纤维释放钙离子。
Biochim Biophys Acta. 1987 Jan 19;927(1):92-9. doi: 10.1016/0167-4889(87)90070-x.
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Kinetics of smooth and skeletal muscle activation by laser pulse photolysis of caged inositol 1,4,5-trisphosphate.通过激光脉冲光解笼化肌醇1,4,5-三磷酸激活平滑肌和骨骼肌的动力学
Nature. 1987;327(6119):249-52. doi: 10.1038/327249a0.
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Inositol 1,4,5-trisphosphate activates pharmacomechanical coupling in smooth muscle of the rabbit mesenteric artery.肌醇1,4,5-三磷酸激活兔肠系膜动脉平滑肌中的药物机械偶联。
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Alteration of calcium sensitivity of skinned frog skeletal muscle fibres by inositol triphosphate and calmodulin antagonists.肌醇三磷酸和钙调蛋白拮抗剂对剥制蛙骨骼肌纤维钙敏感性的影响
Pflugers Arch. 1988 Aug;412(3):253-7. doi: 10.1007/BF00582505.
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Voltage dependence of inositol 1,4,5-trisphosphate-induced Ca2+ release in peeled skeletal muscle fibers.去皮骨骼肌纤维中肌醇1,4,5-三磷酸诱导的Ca2+释放的电压依赖性
Proc Natl Acad Sci U S A. 1988 Aug;85(15):5749-53. doi: 10.1073/pnas.85.15.5749.
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Inositol 1,4,5-trisphosphate activates a channel from smooth muscle sarcoplasmic reticulum.肌醇1,4,5-三磷酸激活平滑肌肌浆网中的一种通道。
Nature. 1988 Dec 8;336(6199):583-6. doi: 10.1038/336583a0.
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Inositol 1,4,5-trisphosphate: a possible chemical link in excitation-contraction coupling in muscle.肌醇1,4,5-三磷酸:肌肉兴奋-收缩偶联中可能的化学联系。
Proc Natl Acad Sci U S A. 1985 Sep;82(18):6352-6. doi: 10.1073/pnas.82.18.6352.

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