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本文引用的文献

1
CHLORIDE IN THE SQUID GIANT AXON.枪乌贼巨大轴突中的氯离子
J Physiol. 1963 Dec;169(3):690-705. doi: 10.1113/jphysiol.1963.sp007289.
2
Movements of Na and K in single muscle fibres.单根肌纤维中钠和钾的运动。
J Physiol. 1959 Mar 3;145(2):405-32. doi: 10.1113/jphysiol.1959.sp006150.
3
The ionic mechanism of intracellular pH regulation in crayfish neurones.小龙虾神经元内pH调节的离子机制。
J Physiol. 1981 Jul;316:293-308. doi: 10.1113/jphysiol.1981.sp013788.
4
Neutral carrier based hydrogen ion selective microelectrode for extra- and intracellular studies.用于细胞外和细胞内研究的基于中性载体的氢离子选择性微电极。
Anal Chem. 1981 Dec;53(14):2267-9. doi: 10.1021/ac00237a031.
5
Na+-H+ exchange at the apical membrane of Necturus gallbladder. Extracellular and intracellular pH studies.美西螈胆囊顶端膜上的钠-氢交换。细胞外和细胞内pH研究。
J Gen Physiol. 1982 Aug;80(2):299-321. doi: 10.1085/jgp.80.2.299.
6
Intracellular pH.细胞内pH值
Physiol Rev. 1981 Apr;61(2):296-434. doi: 10.1152/physrev.1981.61.2.296.
7
Stoichiometry and ion dependencies of the intracellular-pH-regulating mechanism in squid giant axons.鱿鱼巨大轴突中细胞内pH调节机制的化学计量学和离子依赖性。
J Gen Physiol. 1983 Mar;81(3):373-99. doi: 10.1085/jgp.81.3.373.
8
Intracellular pH regulation in the renal proximal tubule of the salamander. Basolateral HCO3- transport.蝾螈肾近端小管中的细胞内pH调节。基底外侧HCO3-转运。
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9
Cl-/HCO3- exchange at the apical membrane of Necturus gallbladder.美西螈胆囊顶端膜上的Cl⁻/HCO₃⁻交换
J Gen Physiol. 1984 Jun;83(6):801-18. doi: 10.1085/jgp.83.6.801.
10
Intracellular ionic activities in the EDL muscle of the mouse.小鼠趾长伸肌中的细胞内离子活性。
Pflugers Arch. 1984 Feb;400(2):166-70. doi: 10.1007/BF00585034.

青蛙骨骼肌细胞内pH调节系统的特性。

Properties of the intracellular pH-regulating systems of frog skeletal muscle.

作者信息

Putnam R W, Roos A, Wilding T J

出版信息

J Physiol. 1986 Dec;381:205-19. doi: 10.1113/jphysiol.1986.sp016323.

DOI:10.1113/jphysiol.1986.sp016323
PMID:3114471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1182975/
Abstract
  1. The properties of the systems that regulate intracellular pH (pHi) in frog muscle (Rana pipiens) were studied in semitendinosus fibres using pH-sensitive micro-electrodes. All experiments were done at 22 degrees C and at external pH (pHo) 7.35. 2. Normally polarized fibres acidified to pHi approximately 6.8 by an NH4Cl pre-pulse (nominal absence of CO2) recovered at a rate of 0.26 +/- 0.04 delta pHi h-1 (n = 10). This corresponds to a net equivalent H ion efflux, JH, of 5.0 pmol cm-2 s-1. This rate was not affected by depolarizing the fibres to -20 mV in 50 mM-K, constant Cl (0.29 +/- 0.03 delta pHi h-1, JH = 4.9 pmol cm-2 s-1, n = 13). Amiloride (1 mM) reduced recovery by almost 90%, while 4-acetamido-4'-isothiocyanostilbene-2,2'-disulphonic acid (SITS, 0.1 mM) reduced recovery by only 18%. Removal of external Na (substitution by N-methyl-D-glucammonium) abolished recovery. Thus, Na-H exchange is responsible for most of the recovery from acidification induced by an NH4Cl pre-pulse. 3. The rate of recovery after an NH4Cl pulse increased linearly as pHi was reduced from 7.25 to 6.55. The dependence of this recovery upon external Na (at pHi 6.90) can be described by Michaelis-Menten kinetics; the apparent Michaelis constant (Km) is 12 +/- 3 mM. 4. Recovery of normally polarized fibres from acidification induced by 5% CO2 is very slow (about 0.03 delta pHi h-1). This recovery could be converted into an acidification of 0.06-0.07 delta pHi h-1 either by removal of Na (as previously described) or by amiloride. We ascribe this acidification of the polarized fibres to HCO3- efflux. 5. In fibres depolarized in 50 mM-K, at constant external Cl concentration, recovery from CO2 acidification was brisk (0.28 +/- 0.01 delta pHi h-1, JH = 9.4 pmol cm-2 s-1, n = 66). It was reduced by about 50% with either SITS or amiloride, and abolished by removal of Na. In the absence of Cl (substituted by gluconate), recovery was also reduced by about 50% and was unaffected by SITS, but nearly abolished by amiloride. Thus, in depolarized fibres, in addition to Na-H exchange, there is an active, SITS-sensitive component of recovery that requires Na, Cl and HCO3.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 使用对pH敏感的微电极,在半腱肌纤维中研究了调节青蛙肌肉(豹蛙)细胞内pH(pHi)的系统特性。所有实验均在22摄氏度和外部pH(pHo)7.35条件下进行。2. 通过氯化铵预脉冲(名义上无二氧化碳)酸化至pHi约为6.8的正常极化纤维,以0.26±0.04ΔpHi h⁻¹的速率恢复(n = 10)。这对应于5.0 pmol cm⁻² s⁻¹的净等效H离子外流,JH。该速率不受在50 mM - K、恒定Cl(0.29±0.03ΔpHi h⁻¹,JH = 4.9 pmol cm⁻² s⁻¹,n = 13)中将纤维去极化至 - 20 mV的影响。氨氯吡脒(1 mM)使恢复降低近90%,而4 - 乙酰氨基 - 4'-异硫氰基芪 - 2,2'-二磺酸(SITS,0.1 mM)仅使恢复降低18%。去除外部Na(用N - 甲基 - D - 葡糖铵替代)消除了恢复。因此,Na - H交换是氯化铵预脉冲诱导酸化后大部分恢复的原因。3. 氯化铵脉冲后的恢复速率随着pHi从7.25降至6.55呈线性增加。这种恢复对外部Na(在pHi 6.90时)的依赖性可用米氏动力学描述;表观米氏常数(Km)为12±3 mM。4. 正常极化纤维从5%二氧化碳诱导的酸化中恢复非常缓慢(约0.03ΔpHi h⁻¹)。通过去除Na(如前所述)或氨氯吡脒,这种恢复可转化为0.06 - 0.07ΔpHi h⁻¹的酸化。我们将极化纤维的这种酸化归因于HCO₃⁻外流。5. 在50 mM - K中去极化、外部Cl浓度恒定的纤维中,从二氧化碳酸化中恢复迅速(0.28±0.01ΔpHi h⁻¹,JH = 9.4 pmol cm⁻² s⁻¹,n = 66)。用SITS或氨氯吡脒处理后,恢复降低约50%,去除Na则消除恢复。在无Cl(用葡萄糖酸盐替代)的情况下,恢复也降低约50%,且不受SITS影响,但几乎被氨氯吡脒消除。因此,在去极化纤维中,除了Na - H交换外,还有一种对SITS敏感的活跃恢复成分,它需要Na、Cl和HCO₃⁻。(摘要截断于400字)