Suppr超能文献

豚鼠离体耳蜗外毛细胞的细胞内pH调节

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

作者信息

Ikeda K, Saito Y, Nishiyama A, Takasaka T

机构信息

Department of Otolaryngology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Physiol. 1992 Feb;447:627-48. doi: 10.1113/jphysiol.1992.sp019021.

Abstract
  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)
摘要
  1. 采用荧光比率成像显微镜研究了从豚鼠分离的外毛细胞(OHC)的细胞内pH(pHi)调节机制。2. 当用HEPES-Tris缓冲的标准溶液灌流时,静息状态下OHC的pHi为7.26±0.08(平均值±标准差,n = 49)。3. 在不存在HCO3-的情况下暴露于25 mM-NH4+会导致pHi发生双相变化;先短暂升高(7.89±0.14,n = 22),随后缓慢下降(7.57±0.12;平均值±标准差)。在不存在HCO3-的情况下引入N-甲基-D-葡糖胺(NMDG+)溶液以去除细胞外NH4+,会使pHi显著酸化至6.38±0.12,几乎没有pHi恢复。随后应用标准Na+溶液可使pHi恢复到初始值。这种恢复受到0.5 mM氨氯吡咪的抑制,但不受0.3 mM 4,4'-二异硫氰酸根合芪-2,2'-二磺酸(DIDS)的抑制。4. 在存在HCO3-的情况下,去除细胞外NH4+和Na+均会迅速导致细胞内酸化,随后pHi恢复。酸负荷后的pHi恢复受到0.3 mM DIDS或10 μM 5-硝基-2-(3-苯丙基氨基)-苯甲酸(NPPB)的抑制。然而,在存在或不存在HCO3-的情况下,添加0.5 mM氨氯吡咪或NMDG+溶液均不会改变稳态下的pHi。5. 从NH +暴露和去除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替代细胞外Cl-会使pHi从7.22±0.12升高至7.51±0.20(n = 6),这受到0.
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17fb/1176055/34f292bc0389/jphysiol00435-0624-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验