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2
The role of intrarenal pH in regulation of ammoniagenesis: [31P]NMR studies of the isolated perfused rat kidney.肾内pH在氨生成调节中的作用:对离体灌注大鼠肾脏的[31P]核磁共振研究
J Physiol. 1981;319:65-79. doi: 10.1113/jphysiol.1981.sp013892.
3
Mechanisms of cation permeation across apical cell membrane of Necturus gallbladder: effects of luminal pH and divalent cations on K+ and Na+ permeability.美洲蟾蜍胆囊顶端细胞膜阳离子渗透机制:管腔pH值和二价阳离子对钾离子和钠离子通透性的影响。
J Membr Biol. 1981 Apr 30;59(3):211-24. doi: 10.1007/BF01875426.
4
Hydrogen ion currents and intracellular pH in depolarized voltage-clamped snail neurones.去极化电压钳制蜗牛神经元中的氢离子电流和细胞内pH值
Nature. 1982 Oct 28;299(5886):826-8. doi: 10.1038/299826a0.
5
Modifier role of internal H+ in activating the Na+-H+ exchanger in renal microvillus membrane vesicles.肾微绒毛膜囊泡中内部H⁺在激活钠氢交换体中的调节作用
Nature. 1982 Sep 9;299(5879):161-3. doi: 10.1038/299161a0.
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
Inhibition of the serum-dependent, amiloride-sensitive sodium transport pathway in human fibroblasts by extracellular divalent cations.
J Cell Physiol. 1982 May;111(2):163-70. doi: 10.1002/jcp.1041110207.
8
Aequorin-calcium transients in frog twitch muscle fibres.青蛙抽动肌纤维中的水母发光蛋白 - 钙瞬变
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9
The intracellular pH of frog skeletal muscle: its regulation in hypertonic solutions.青蛙骨骼肌的细胞内pH值:其在高渗溶液中的调节
J Physiol. 1983 Dec;345:189-204. doi: 10.1113/jphysiol.1983.sp014974.
10
The intracellular pH of frog skeletal muscle: its regulation in isotonic solutions.青蛙骨骼肌的细胞内pH值:其在等渗溶液中的调节
J Physiol. 1983 Dec;345:175-87. doi: 10.1113/jphysiol.1983.sp014973.

钙及其他二价阳离子对青蛙骨骼肌细胞内pH调节的影响。

Effect of calcium and other divalent cations on intracellular pH regulation of frog skeletal muscle.

作者信息

Putnam R W, Roos A

出版信息

J Physiol. 1986 Dec;381:221-39. doi: 10.1113/jphysiol.1986.sp016324.

DOI:10.1113/jphysiol.1986.sp016324
PMID:3114472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1182976/
Abstract
  1. We examined, in frog semitendinosus muscle, the effect of calcium release, induced by depolarization or caffeine, on intracellular pH (pHi) recovery from an acid load applied at least 40 min later. We also studied the effect of external Ca and other divalent cations on recovery. We used pH-sensitive micro-electrodes; the external pH (pHo) was always 7.35. 2. In fibres depolarized by 50 mM-K, constant [K] X [Cl] in the presence of 1 mM-tetracaine (which blocks Ca release), the rate of pHi recovery from 5% CO2-induced acidification was 0.15 +/- 0.02 delta pHi h-1 (n = 7), whereas in depolarized fibres that had never been exposed to the drug, the rate of recovery was 0.27 +/- 0.01 delta pHi h-1 (n = 5). Yet, when Ca release was not blocked and the depolarized fibres were exposed to tetracaine shortly before CO2 exposure, a similar slow rate of 0.14 +/- 0.03 delta pHi h-1 (n = 7) was observed. When Ca release was blocked by tetracaine, but the drug washed out before recovery, the rate was again 0.27 +/- 0.02 delta pHi h-1 (n = 6). 3. In fibres first depolarized to about -23 mV in 50 mM-K, constant [K] X [Cl] (recovery of 0.23 +/- 0.03 delta pHi h-1, n = 6), and then repolarized to -79 mV in 2.5 mM-K, the slow rate of recovery was the same (0.03 +/- 0.02 delta pHi h-1) as that in fibres without a history of depolarization and thus of Ca release. 4. In fibres depolarized to -50 mV (15 mM-K, constant Cl) and then exposed to caffeine (4 mM) which releases Ca from intracellular stores, the recovery was the same (0.07 +/- 0.03 delta pHi h-1, n = 5) as in depolarized fibres not exposed to caffeine (0.09 +/- 0.01 delta pHi h-1, n = 5). 5. We conclude that in frog muscle transient Ca release induced by either depolarization or caffeine does not affect the rate of subsequent pHi recovery. Tetracaine reversibly inhibits pHi recovery, but this inhibition is not due to its blocking of Ca release. 6. Recovery from CO2-induced acidification of fibres depolarized to -21 mV in 50 mM-K, constant Cl was halved, from 0.31 +/- 0.04 delta pHi h-1 (n = 10) to 0.15 +/- 0.01 delta pHi h-1 (n = 13), when external Ca was raised from 4 to 10 mM.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 我们在青蛙半腱肌中研究了由去极化或咖啡因诱导的钙释放,对至少40分钟后施加酸负荷后细胞内pH(pHi)恢复的影响。我们还研究了细胞外钙和其他二价阳离子对恢复的影响。我们使用了对pH敏感的微电极;细胞外pH(pHo)始终为7.35。2. 在由50 mM - K去极化、在1 mM - 丁卡因(阻断钙释放)存在下保持[K]×[Cl]恒定的纤维中,从5% CO₂诱导的酸化中恢复pHi的速率为0.15±0.02 ΔpHi h⁻¹(n = 7),而在从未接触过该药物的去极化纤维中,恢复速率为0.27±0.01 ΔpHi h⁻¹(n = 5)。然而,当钙释放未被阻断且在CO₂暴露前不久将去极化纤维暴露于丁卡因时,观察到类似的缓慢速率,为0.14±0.03 ΔpHi h⁻¹(n = 7)。当钙释放被丁卡因阻断,但在恢复前将药物洗脱时,速率再次为0.27±0.02 ΔpHi h⁻¹(n = 6)。3. 在首先在50 mM - K、恒定[K]×[Cl]中去极化至约 - 23 mV(恢复速率为0.23±0.03 ΔpHi h⁻¹,n = 6),然后在2.5 mM - K中复极化至 - 79 mV的纤维中,恢复的缓慢速率与没有去极化和钙释放历史的纤维相同(0.03±0.02 ΔpHi h⁻¹)。4. 在去极化至 - 50 mV(15 mM - K,恒定Cl)然后暴露于从细胞内储存释放钙的咖啡因(4 mM)的纤维中,恢复情况与未暴露于咖啡因的去极化纤维相同(0.07±0.03 ΔpHi h⁻¹,n = 5)(0.09±0.01 ΔpHi h⁻¹,n = 5)。5. 我们得出结论,在青蛙肌肉中,由去极化或咖啡因诱导的瞬时钙释放不影响随后pHi恢复的速率。丁卡因可逆地抑制pHi恢复,但这种抑制不是由于其阻断钙释放。6. 当细胞外钙从4 mM升高到10 mM时,在50 mM - K、恒定Cl中去极化至 - 21 mV的纤维从CO₂诱导的酸化中恢复的速率减半,从0.31±0.04 ΔpHi h⁻¹(n = 10)降至0.15±0.01 ΔpHi h⁻¹(n = 13)。(摘要截断于400字)