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Intracellular pH regulation in isolated cochlear outer hair cells of the guinea-pig.

机译:豚鼠离体耳蜗外毛细胞的细胞内pH调节。

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摘要

1. The intracellular pH (pHi) regulation mechanisms of the outer hair cell (OHC) isolated from the guinea-pig were studied using fluorescence ratio imaging microscopy. 2. The OHC pHi in the resting condition was 7.26 +/- 0.08 (mean +/- S.D., n = 49) when the standard solution buffered with HEPES-Tris was superfused. 3. Exposure to 25 mM-NH4+ in the absence of HCO3- caused biphasic changes in pHi; a transient increase (7.89 +/- 0.14, n = 22) followed by a slow decrease (7.57 +/- 0.12; mean +/- S.D.). Removal of external NH4+ by introducing the N-methyl-D-glucamine (NMDG+) solution in the absence of HCO3- markedly acidified the pHi to 6.38 +/- 0.12 with little pHi recovery. Subsequent application of the standard Na+ solution restored the pHi to the initial value. The recovery was inhibited by 0.5 mM-amiloride but not by 0.3 mM-DIDS (4,4'-diisothiocyanatostilbene-2,2'-disulphonic acid). 4. In the presence of HCO3-, removal of both external NH4+ and Na+ promptly caused an intracellular acidification followed by a pHi recovery. The pHi recovery from an acid load was inhibited by 0.3 mM-DIDS or 10 microM-NPPB (5-nitro-2-(3-phenylpropyl-amino)-benzoate). However, the pHi in the steady state in the presence or absence of HCO3- was not altered by addition of 0.5 mM-amiloride or NMDG+ solution. 5. The intracellular buffering power obtained from the NH4+ exposure and withdrawal was -15.1 +/- 8.7 mM (pH unit)-1 (n = 6) and -14.3 +/- 5.8 mM (pH unit)-1, respectively. 6. Replacement of external Cl- with gluconate in the HCO3- solution increased the pHi from 7.22 +/- 0.12 to 7.51 +/- 0.20 (n = 6), which was inhibited by 0.3 mM-DIDS. Moreover, addition of DIDS to the HCO3- solution increased the pHi by 0.13 +/- 0.08 (n = 8). 7. When the external standard solution buffered with HEPES-Tris was replaced with the HCO3- solution, the basal pHi (7.27 +/- 0.10) was promptly acidified to 6.87 +/- 0.10 then relaxed slowly to 7.00 +/- 0.15 (n = 16). 8. The pHi showed an initial alkalinization and a subsequent slow acidification after the HCO3(-)-free standard solution replaced the HCO3- solution. The slow acidification was inhibited by low external Cl- concentration or by addition of 0.3 mM-DIDS.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.使用荧光比率成像显微镜研究了从豚鼠中分离的外毛细胞(OHC)的细胞内pH(pHi)调节机制。 2.当融合有HEPES-Tris缓冲液的标准溶液时,静止状态下的OHC pHi为7.26 +/- 0.08(平均+/- S.D.,n = 49)。 3.在不存在HCO3-的情况下暴露于25 mM-NH4 +会引起pHi的双相变化;短暂增加(7.89 +/- 0.14,n = 22),然后缓慢降低(7.57 +/- 0.12;平均值+/- S.D.)。通过在不存在HCO3的情况下引入N-甲基-D-葡糖胺(NMDG +)溶液来去除外部NH4 +,可将pHi酸化至6.38 +/- 0.12,几乎不会回收pHi。随后应用标准Na +溶液可将pHi恢复至初始值。 0.5 mM-阿米洛利抑制了恢复,但0.3 mM-DIDS(4,4'-二异硫氰酸根合二苯乙烯-2,2'-二磺酸)抑制了回收率。 4.在存在HCO3-的情况下,去除外部NH4 +和Na +会迅速引起细胞内酸化,然后恢复pHi。 0.3 mM-DIDS或10 microM-NPPB(5-硝基-2-(3-苯基丙基-氨基)-苯甲酸酯)抑制了从酸性负载中回收pHi。但是,在存在或不存在HCO3-的情况下,稳态pHi不会因添加0.5 mM-阿米洛利或NMDG +溶液而改变。 5.从NH 4 +暴露和撤出获得的细胞内缓冲能力分别为-15.1 +/- 8.7 mM(pH单位)-1(n = 6)和-14.3 +/- 5.8 mM(pH单位)-1。 6.在HCO3-溶液中用葡萄糖酸盐代替外部Cl-使pHi从7.22 +/- 0.12增加到7.51 +/- 0.20(n = 6),这被0.3 mM-DIDS抑制。此外,向HCO3-溶液中添加DIDS使pHi增加了0.13 +/- 0.08(n = 8)。 7.当将用HEPES-Tris缓冲的外标溶液替换为HCO3-溶液时,基础pHi(7.27 +/- 0.10)立即酸化至6.87 +/- 0.10,然后缓慢松弛至7.00 +/- 0.15(n = 16)。 8.在不含HCO3(-)的标准溶液代替HCO3-溶液后,pHi表现出初始碱化和随后的缓慢酸化。低的外部Cl浓度或添加0.3 mM-DIDS抑制了缓慢的酸化。(摘要截短了400字)

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