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本文引用的文献

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The hydrogen ion concentration of the muscles of the cat.猫肌肉的氢离子浓度。
J Physiol. 1927 Jun 7;63(1):33-41. doi: 10.1113/jphysiol.1927.sp002378.
2
INTRACELLULAR ACID-BASE REGULATION. I. THE RESPONSE OF MUSCLE CELLS TO CHANGES IN CO2 TENSION OR EXTRACELLULAR BICARBONATE CONCENTRATION.细胞内酸碱调节。I. 肌肉细胞对二氧化碳张力或细胞外碳酸氢盐浓度变化的反应。
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Solubility of ammonia in human plasma.氨在人体血浆中的溶解度。
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The pH of K-deficient muscle.低钾肌肉的pH值。
Am J Physiol. 1959 Apr;196(4):811-8. doi: 10.1152/ajplegacy.1959.196.4.811.
5
Intramitochondrial pH and intra-extramitochondrial pH gradient of beef heart mitochondria in various functional states.处于不同功能状态的牛心线粒体的线粒体内pH值及线粒体内外pH梯度。
Nature. 1967 Apr 22;214(5086):400-2. doi: 10.1038/214400b0.
6
Measurement of intracellular pH of skeletal muscle with pH-sensitive glass microelectrodes.使用pH敏感玻璃微电极测量骨骼肌细胞内pH值。
J Clin Invest. 1967 Jun;46(6):920-33. doi: 10.1172/JCI105598.
7
Carbon dioxide dissociation curve in potassium depletion.低钾血症时的二氧化碳解离曲线
Am J Physiol. 1967 Apr;212(4):953-6. doi: 10.1152/ajplegacy.1967.212.4.953.
8
In vivo CO-2 buffer curves of skeletal and cardiac muscle.骨骼肌和心肌的体内二氧化碳缓冲曲线。
Am J Physiol. 1966 Dec;211(6):1309-12. doi: 10.1152/ajplegacy.1966.211.6.1309.
9
Direct intracellular pH measurement in rat and crab muscle.大鼠和蟹肌肉细胞内pH值的直接测量
J Physiol. 1972 Jun;223(2):297-319. doi: 10.1113/jphysiol.1972.sp009848.
10
Determination of intracellular buffering properties in rat diaphragm muscle.大鼠膈肌细胞内缓冲特性的测定
Am J Physiol. 1972 Mar;222(3):747-53. doi: 10.1152/ajplegacy.1972.222.3.747.

小鼠比目鱼肌纤维细胞内pH值和缓冲能力的微电极测量

Micro-electrode measurement of the intracellular pH and buffering power of mouse soleus muscle fibres.

出版信息

J Physiol. 1977 Jun;267(3):791-810. doi: 10.1113/jphysiol.1977.sp011838.

DOI:10.1113/jphysiol.1977.sp011838
PMID:17740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1283640/
Abstract
  1. The intracellular pH (pHi) of surface fibres of the mouse soleus muscle has been measured in vitro using recessed-tip pH-sensitive microelectrodes. 2. In 5% CO2 and pH 7-40, the mean pHi was 7-07 +/- 0-007 (S.E. of mean) at 37 degrees C and 7-23 +/- 0-01 at 28 degrees C. The difference between these tow values is the same as the change in neutral pH between 37 and 28 degrees C. 3. Alteration of the CO2 level at constant external pH caused a biphasic change in pHi with a rapid displacement followed by a slower partial recovery. Because the recovery was incomplete, different stable pHi values were recorded at different CO2 levels, the higher the CO2 the lower the pHi. The differences in pHi were highly significant both at 37 and 28 degrees C. 4. Alteration of the CO2 level at constant external pH also changed the membrane potential (Em), an increase in CO2 leading to an increased Em. The dependence of Em on the CO2 level was much smaller in the fast-twitch muscle, extensor digitorum longus, than in soleus. 5. Changing external pH, either by alteration of the bicarbonate or CO2 level of the Ringer solution, caused pHi to change by a mean 38-7% of the external pH change. The change in pHi was accomplished about 10 times more rapidly, and in the same direction, by altering CO2 than by altering the bicarbonate. 6. Application of external NH3 and NH+4 caused a rapid intracellular alkalinization followed by a slower acidification. On removal of external NH3 and NH+4, there was a large and rapid acdification, followed by a fairly rapid recovery in pHi. 7. The size of the pHi changes occurring on alteration of the CO2 level at both constant external pH and constant external bicarbonate, and on removal of external NH3 and NH+4, suggests a non-CO2 buffering power of 45m-equiv H+ ions/pH unit per litre and a constant-CO2 buffering power of 58 m-equiv H+ ions/pH unit per litre. The buffering power was apparently unaffected by a change in temperature between 37 and 28 degrees C. 8. It was concluded that H+ ions are not passively distributed across the muscle cell membrane, and that the pHi is closely controlled by the active transport of H+, OH- or HCO-3 ions.
摘要
  1. 已使用凹形尖端pH敏感微电极在体外测量了小鼠比目鱼肌表面纤维的细胞内pH值(pHi)。2. 在5%二氧化碳和pH 7.40条件下,37℃时平均pHi为7.07±0.007(平均值的标准误),28℃时为7.23±0.01。这两个值之间的差异与37℃至28℃之间中性pH值的变化相同。3. 在恒定外部pH值下改变二氧化碳水平会导致pHi出现双相变化,先是快速偏移,随后是较慢的部分恢复。由于恢复不完全,在不同二氧化碳水平下记录到不同的稳定pHi值,二氧化碳水平越高,pHi越低。在37℃和28℃时,pHi的差异都非常显著。4. 在恒定外部pH值下改变二氧化碳水平也会改变膜电位(Em),二氧化碳增加会导致Em升高。在快肌(趾长伸肌)中,Em对二氧化碳水平的依赖性比对比目鱼肌小得多。5. 通过改变任氏液的碳酸氢盐或二氧化碳水平来改变外部pH值,会使pHi平均改变外部pH值变化的38.7%。通过改变二氧化碳来改变pHi的速度比通过改变碳酸氢盐快约10倍,且方向相同。6. 施加外部NH₃和NH₄⁺会导致细胞内迅速碱化,随后是较慢的酸化。去除外部NH₃和NH₄⁺后,会出现大量快速酸化,随后pHi相当迅速地恢复。7. 在恒定外部pH值和恒定外部碳酸氢盐条件下改变二氧化碳水平,以及去除外部NH₃和NH₄⁺时发生的pHi变化大小,表明非二氧化碳缓冲能力为每升45毫当量H⁺离子/pH单位,恒定二氧化碳缓冲能力为每升58毫当量H⁺离子/pH单位。缓冲能力显然不受37℃至28℃温度变化的影响。8. 得出的结论是,H⁺离子不是被动地分布在肌细胞膜上,并且pHi受到H⁺、OH⁻或HCO₃⁻离子主动转运的密切控制。