J Physiol Society Meetings
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 409 pp 89-101
Copyright © 1989 by The Physiological Society
This Article
Right arrow Full Text (PDF)
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Szatkowski, M S
Right arrow Articles by Thomas, R C
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Szatkowski, M S
Right arrow Articles by Thomas, R C

The intrinsic intracellular H+ buffering power of snail neurones.

M S Szatkowski and R C Thomas

Department of Physiology, University of Bristol.

1. We measured intracellular pH (pHi) in snail neurones using pH-sensitive glass microelectrodes. We then calculated the intracellular buffering power (beta i) from the pHi changes associated with the influx or efflux of a variety of weak acids or bases. 2. The weak acid anions butyrate and propionate (20 mM) gave similar values for beta i but those measured using 20 mM-acetate were on average twice as great. 3. Although solutions were nominally CO2-free, blockage of pHi regulation with SITS (4-acetamido-4'-isothiocyanatostilbene-2,2'-disulphonic acid) increased the sizes of the pHi changes upon weak acid addition and removal. The corresponding measured values of beta i were on average 26% lower with SITS than without. 4. With pHi regulation blocked, the use of 2.7% CO2 to measure beta i gave beta i values similar to those measured with butyrate or propionate. These values were about 50% less than those previously measured in snail neurones using CO2. 5. beta i values calculated from the pHi changes due to the removal of 5 mM of the weak bases trimethylamine, procaine and NH4Cl were all similar and comparable to those measured using butyrate or propionate. Removing the influence of pHi regulation on the undershoots after NH4Cl removal was found to decrease the apparent measured values of beta i by 10%. 6. Combining all the data (except the values obtained using CO2 and acetate), and adjusting for the errors due to pHi regulation reducing the sizes of the pHi changes, we found that the mean value for beta i was 10.4 +/- 0.6 mM (+/- S.E.M.) at a mean pHi of 7.36 +/- 0.05. 7. We also investigated the relationship between beta i and pHi using ionophoretic acid injection. By means of step-wise injections, with pHi regulation blocked, we found that at normal pHi levels beta i remained relatively constant. However, at a pHi of less than about 6.8 beta i increased with decreasing pHi.




This article has been cited by other articles:


Home page
Anesth. Analg.Home page
S. Onizuka, T. Kasaba, R. Tamura, and M. Takasaki
Lidocaine Increases Intracellular Sodium Concentration Through a Na+-H+ Exchanger in an Identified Lymnaea Neuron
Anesth. Analg., May 1, 2008; 106(5): 1465 - 1472.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
L. Stuwe, M. Muller, A. Fabian, J. Waning, S. Mally, J. Noel, A. Schwab, and C. Stock
pH dependence of melanoma cell migration: protons extruded by NHE1 dominate protons of the bulk solution
J. Physiol., December 1, 2007; 585(2): 351 - 360.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M. E. Mycielska and M. B. A. Djamgoz
Citrate transport in the human prostate epithelial PNT2-C2 cell line: electrophysiological analyses
J. Physiol., September 15, 2004; 559(3): 821 - 833.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
W. Zeiske, H. Meyer, and H. Wieczorek
Insect midgut K+ secretion: concerted run-down of apical/basolateral transporters with extra-/intracellular acidity
J. Exp. Biol., February 15, 2002; 205(4): 463 - 474.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
M.-L. Wu, C.-C. Chan, and M.-J. Su
Possible Mechanism(s) of Arachidonic Acid-Induced Intracellular Acidosis in Rat Cardiac Myocytes
Circ. Res., February 18, 2000; 86 (3): e55 - e62.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
C. J. Schwiening and D. Willoughby
Depolarization-induced pH microdomains and their relationship to calcium transients in isolated snail neurones
J. Physiol., January 9, 2002; 538(2): 371 - 382.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1989 The Physiological Society.