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蛙骨骼肌中钾离子通量途径的亚细胞定位。

The subcellular location of potassium flux pathways in frog skeletal muscle.

作者信息

Kovács T, Pfliegler G, Szabó B

出版信息

Pflugers Arch. 1981 Jun;390(3):250-5. doi: 10.1007/BF00658270.

Abstract

The influence of ouabain and physostigmine on 42K and 86Rb uptake in isolated from sartorii with normal [Na]i(12-14 mmol.kg -1 wet weight) and low [Na]i (6 mmol.kg-1 wet weight) was compared. Both in normal sodium and in low sodium muscles application of 10-3 M physostigmine reduces potassium influx by about 70%. About one forth of potassium-uptake in normal-sodium muscles is inhibited by ouabain (10-4 M) and only a very slight fraction of potassium uptake is ouabain-sensitive in low-sodium muscle. The effects of ouabain and physostigmine on 42K influx are additive. The greater parts of the Rb-fluxes are through the ouabain-sensitive pathway. Glycerol treatment has no effect on ouabain-sensitive channels although it inhibits markedly the K-flux through the physostigmine-sensitive pathway. The results suggest that the Na-K-ATPase is located in the surface membrane while most of the physostigmine-sensitive K-exchange is within the tubules.

摘要

比较了哇巴因和毒扁豆碱对正常[Na]i(12 - 14 mmol·kg-1湿重)和低[Na]i(6 mmol·kg-1湿重)的离体缝匠肌摄取42K和86Rb的影响。在正常钠和低钠肌肉中,应用10-3 M毒扁豆碱均可使钾离子内流减少约70%。哇巴因(10-4 M)抑制正常钠肌肉中约四分之一的钾摄取,而在低钠肌肉中只有非常小部分的钾摄取对哇巴因敏感。哇巴因和毒扁豆碱对42K内流的作用是相加的。大部分铷通量是通过对哇巴因敏感的途径。甘油处理对哇巴因敏感通道无影响,尽管它显著抑制了通过毒扁豆碱敏感途径的钾通量。结果表明,钠钾ATP酶位于表面膜,而大部分对毒扁豆碱敏感的钾交换在小管内。

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