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The regulation of intracellular pH by identified glial cells and neurones in the central nervous system of the leech.
Author(s) -
Deitmer J W,
Schlue W R
Publication year - 1987
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1987.sp016614
Subject(s) - leech , hirudo medicinalis , intracellular ph , hepes , saline , biophysics , intracellular , chemistry , anatomy , biology , microbiology and biotechnology , biochemistry , endocrinology , world wide web , computer science
1. Double‐barrelled, neutral‐carrier pH‐sensitive micro‐electrodes were used to measure the intracellular pH (pHi) and the pHi regulation of neuropile glial (n.g.) cells and of identified neurones of the leech Hirudo medicinalis. 2. The distribution of H+ in the n.g. cells and in the neurones was found not to be in electrical equilibrium. The mean pHi of the n.g. cells was 6.87 +/‐ 0.13 (mean +/‐ S.D. of mean here and for all following data n = 27) in HEPES‐buffered leech saline (pHo = 7.4) and 7.18 +/‐ 0.19 (n = 13) in 2% CO2‐11 mM‐HCO3(‐)‐saline. The mean pHi was 7.28 +/‐ 0.1 (n = 20) in Retzius neurones and 7.32 +/‐ 0.15 (n = 12) in noxious neurones in HEPES‐buffered leech saline, and 7.20 +/‐ 0.15 (n = 10) and 7.27 +/‐ 0.16 (n = 6) in 2% CO2‐11 mM‐HCO3(‐)‐buffered saline in these two types of neurones, respectively. 3. The cytoplasmic buffering power, as calculated by the change in pHi following the change from 2% CO2‐11 mM‐HCO3‐ to 5% CO2‐22 mM‐HCO3‐ in the leech saline, was 20‐30 mM/pH unit in the n.g. cells and between 12 and 33 mM/pH unit in the neurones. 4. The recovery of pHi in n.g. cells from an experimentally induced acidification (addition and removal of 20 mM‐NH4Cl) was dependent on the presence of external Na+. Independent of the buffer system used, pHi recovery was inhibited when external Na+ was exchanged by N‐methyl‐D‐glucamine. Amiloride (2‐3 mM) reduced the rate of pHi recovery by about 50% in these n.g. cells. 5. In CO2‐HCO3(‐)‐free saline, or in the presence of the anion exchange blocker 4‐acetamido‐4'‐isothiocyanostilbene‐2, 2'‐disulphonic acid (SITS, 0.5 mM), pHi recovery from an acid load was often slowed by up to 50% in n.g. cells. This suggests that there is a significant contribution of a HCO3(‐)‐dependent membrane transport to pHi regulation in n.g. cells. 6. When a HEPES‐buffered saline was exchanged by a 2% CO2‐11 mM‐HCO3(‐)‐buffered saline, the pHi of n.g. cells increased by 0.31 pH units. This alkaline shift was reversible upon removal of the CO2‐HCO3‐ and was absent in the Na+‐free saline. It was not inhibited by 1 mM‐furosemide or by 0.5 mM‐SITS.(ABSTRACT TRUNCATED AT 400 WORDS)