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本文引用的文献

1
The effect of external sodium concentration on the sodium fluxes in frog skeletal muscle.外部钠浓度对青蛙骨骼肌钠通量的影响。
J Physiol. 1959 Oct;147(3):591-625. doi: 10.1113/jphysiol.1959.sp006264.
2
THE POTASSIUM FLUX RATIO IN SKELETAL MUSCLE AS A TEST FOR INDEPENDENT ION MOVEMENT.骨骼肌中的钾通量比率作为独立离子运动的一项测试
J Gen Physiol. 1965 May;48(5):777-95.
3
THE CONTROL OF THE MEMBRANE POTENTIAL OF MUSCLE FIBERS BY THE SODIUM PUMP.钠泵对肌纤维膜电位的控制
J Gen Physiol. 1965 May;48(5):761-75. doi: 10.1085/jgp.48.5.761.
4
EFFECTS OF EXTERNAL POTASSIUM AND STROPHANTHIDIN ON SODIUM FLUXES IN FROG STRIATED MUSCLE.外源性钾离子和毒毛旋花子苷对蛙横纹肌钠通量的影响
J Gen Physiol. 1965 Jan;48(3):489-514. doi: 10.1085/jgp.48.3.489.
5
Factors influencing the sodium movement in frog muscle with a discussion of the mechanism of sodium movement.影响蛙肌中钠运动的因素,并对钠运动机制进行讨论。
J Physiol. 1957 Mar 11;135(3):567-80. doi: 10.1113/jphysiol.1957.sp005731.
6
Influence of ouabain, strophanthidin and dihydrostrophanthidin on sodium and potassium transport in frog sartorii.哇巴因、毒毛花苷元和二氢毒毛花苷元对蛙缝匠肌钠钾转运的影响
Am J Physiol. 1956 Nov;187(2):328-32. doi: 10.1152/ajplegacy.1956.187.2.328.
7
The energy requirement for sodium extrusion from a frog muscle.从蛙肌中挤出钠所需的能量。
Proc R Soc Lond B Biol Sci. 1954 May 27;142(908):383-92. doi: 10.1098/rspb.1954.0031.
8
Membrane potential and conductance during transport of sodium, potassium and rubidium in frog muscle.蛙肌中钠、钾和铷转运过程中的膜电位与电导率
J Physiol. 1966 Jun;184(4):970-1014. doi: 10.1113/jphysiol.1966.sp007961.

受细胞内钠浓度影响的骨骼肌中钾和钠转运的毒毛花苷元敏感成分。

Strophanthidin-sensitive components of potassium and sodium movements in skeletal muscle as influenced by the internal sodium concentration.

作者信息

Sjodin R A, Beaugé L A

出版信息

J Gen Physiol. 1968 Sep;52(3):389-407. doi: 10.1085/jgp.52.3.389.

DOI:10.1085/jgp.52.3.389
PMID:5673300
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2225818/
Abstract

"Low sodium" muscles were prepared which contained around 5 mmoles/kg fiber of intracellular sodium. "High sodium" muscles containing between 15 and 30 mmoles/kg fiber of intracellular sodium were also prepared. In low sodium muscles application of 10(-5)M strophanthidin reduced potassium influx by about 5%. Potassium efflux was unaffected by strophanthidin under these conditions. In high sodium muscles, 10(-5)M strophanthidin reduced potassium influx by 45% and increased potassium efflux by 70%, on the average. In low sodium muscles sodium efflux was reduced by 25% during application of 10(-5)M strophanthidin while in high sodium muscles similarly treated, sodium efflux was reduced by about 60%. Low sodium muscles showed a large reduction in sodium efflux when sodium ions in the Ringer solution were replaced by lithium ions. The average reduction in sodium efflux was 4.5-fold. Of the amount of sodium efflux remaining in lithium. Ringer's solution, 40% could be inhibited by application of 10(-5)M strophanthidin. The total sodium efflux from low sodium muscles exposed to Ringer's solution in which lithium had been substituted for sodium ions for a period of 1 hr can be fractionated as 78% Na-for-Na interchange, 10% strophanthidin-sensitive sodium pump, and 12% residual sodium efflux. It is concluded that large strophanthidin-sensitive components of sodium and potassium flux can be expected only at elevated sodium concentrations within the muscle cells.

摘要

制备了“低钠”肌肉,其细胞内钠含量约为5毫摩尔/千克纤维。还制备了“高钠”肌肉,其细胞内钠含量在15至30毫摩尔/千克纤维之间。在低钠肌肉中,施加10⁻⁵M毒毛花苷可使钾离子内流减少约5%。在这些条件下,毒毛花苷对钾离子外流没有影响。在高钠肌肉中,10⁻⁵M毒毛花苷平均使钾离子内流减少45%,使钾离子外流增加70%。在低钠肌肉中,施加10⁻⁵M毒毛花苷时,钠离子外流减少25%;而在同样处理的高钠肌肉中,钠离子外流减少约60%。当任氏溶液中的钠离子被锂离子取代时,低钠肌肉的钠离子外流大幅减少。钠离子外流的平均减少倍数为4.5倍。在锂任氏溶液中剩余的钠离子外流中,40%可被施加10⁻⁵M毒毛花苷所抑制。暴露于钠离子被锂离子取代1小时的任氏溶液中的低钠肌肉的总钠离子外流可分为78%的钠-钠交换、10%的毒毛花苷敏感钠泵和12%的残余钠离子外流。得出的结论是,只有在肌肉细胞内钠浓度升高时,才可能出现大量对毒毛花苷敏感的钠和钾通量成分。