Home LiteratureArticle Details
PMID: 2170631 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

pH dependence of intrinsic H+ buffering power in the sheep cardiac Purkinje fibre.

The Journal of physiology ·Vol. 425 ·1990-06-00 ·Pages 429-48

Vaughan-Jones RD, Wu ML

Abstract

1. Intrinsic, intracellular H+ buffering power (beta) was estimated in the isolated sheep cardiac Purkinje fibre at various values of intracellular pH (pHi) in the range 6.2-7.5 and for various values of extracellular pH (pHo) in the range 6.5-8.5. Buffering power was calculated from the fall of pHi (recorded with an intracellular pH-selective microelectrode) induced by addition and removal of extracellular, permeant weak acids and bases (NH4Cl, trimethylamine chloride, sodium propionate). Experiments were performed under conditions nominally free of CO2-HCO3. 2. beta was estimated firstly following acid loads induced by NH4Cl removal (10-20 mM) under conditions where Na(+)-H+ exchange was operational (i.e. in Na(+)-containing Tyrode solution). At constant pHi, the value of beta appeared to double (from a control level of 39.7 mM) as pHo was increased from 7.5 to 8.5. Notably, raising pHo in this range greatly accelerated pHi recovery from an intracellular acid load, indicating stimulation of acid extrusion. It is likely that this stimulation results in an overestimation of beta because it blunts the intracellular acid load. The apparent elevation of beta at high pHo may therefore be an artifact. 3. Estimates of beta were compared (NH4Cl removal) before and after inhibiting Na(+)-H+ exchange in Na(+)-free solution or with amiloride (1 mM). The acid load was larger and in many (but not all) cases the apparent value of beta decreased after inhibition of acid extrusion. This indicates that, if Na(+)-H+ exchange is operational, it can result in an overestimate of beta. In amiloride, beta was 26.6 +/- 1.4 mM (n = 8) at a mean pHi of 6.84 +/- 0.03. 4. Small stepwise reductions of external NH4Cl (from 40 to 0 mM), in the presence of Na(+)-free solution plus 5 mM-BaCl2 at constant pHo, resulted in small stepwise reductions of pHi (approximately 0.1 units). When these were used to calculate beta, we observed that beta increased roughly linearly as pHi became more acid. For a pHi of 7.2, beta approximately 20 mM. 5. An almost identical relationship between beta and pHi was found when using the method of sodium propionate addition (10-50 mM): amiloride (1 mM) was present and pHi was manipulated to various test levels by changing pHo. This confirms that beta varies inversely with pHi and also that it is independent of pHo. We conclude that the apparent variation of beta with pHo observed earlier was indeed an artifact.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Amiloride/pharmacology Ammonium Chloride/pharmacology Animals Buffers Hydrogen-Ion Concentration Ion Exchange Membrane Potentials Microelectrodes Protons Purkinje Fibers/physiology Sheep
Chemicals
Buffers Protons Ammonium Chloride Amiloride
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Vaughan-Jones R D
University Laboratory of Physiology, Oxford.
Wu M L
References (25)
25 references, click to expand
  1. Direct measurement of the intracellular pH of mammalian cardiac muscle.
    J Physiol. 1976 Nov;262(3):755-71 PMID: 13205
  2. The effect of carbon dioxide on the intracellular pH and buffering power of snail neurones.
    J Physiol. 1976 Mar;255(3):715-35 PMID: 4614
  3. Micro-electrode measurement of the intracellular pH and buffering power of mouse soleus muscle fibres.
    J Physiol. 1977 Jun;267(3):791-810 PMID: 17740
  4. Regulation of chloride in quiescent sheep-heart Purkinje fibres studied using intracellular chloride and pH-sensitive micro-electrodes.
    J Physiol. 1979 Oct;295:111-37 PMID: 42779
  5. Interactions between the regulation of the intracellular pH and sodium activity of sheep cardiac Purkinje fibres.
    J Physiol. 1980 Jul;304:471-88 PMID: 7441547
  6. Intracellular pH.
    Physiol Rev. 1981 Apr;61(2):296-434 PMID: 7012859
  7. Direct measurement of intracellular pH and buffering power in smooth muscle cells of guinea-pig vas deferens.
    J Physiol. 1984 Apr;349:571-85 PMID: 6429320
  8. Na/H exchange in cultured chick heart cells. pHi regulation.
    J Gen Physiol. 1985 Jan;85(1):43-64 PMID: 3968533
  9. Kinetic properties of the plasma membrane Na+-H+ exchanger.
    Annu Rev Physiol. 1985;47:545-60 PMID: 2581505
  10. Biochemical properties of the Na+/H+ exchange system in rat brain synaptosomes. Interdependence of internal and external pH control of the exchange activity.
    J Biol Chem. 1985 Aug 15;260(17):9678-84 PMID: 2991259
  11. Influence of surface pH on intracellular pH regulation in cardiac and skeletal muscle.
    Am J Physiol. 1986 May;250(5 Pt 1):C748-60 PMID: 3085512
  12. A novel experimental chamber for single-cell voltage-clamp and patch-clamp applications with low electrical noise and excellent temperature and flow control.
    Pflugers Arch. 1986 May;406(5):536-9 PMID: 3714452
  13. The sensitivity of liquid sensor, ion-selective microelectrodes to changes in temperature and solution level.
    Pflugers Arch. 1986 Jun;406(6):641-4 PMID: 3714459
  14. An investigation of chloride-bicarbonate exchange in the sheep cardiac Purkinje fibre.
    J Physiol. 1986 Oct;379:377-406 PMID: 3559998
  15. Effect of repetitive activity upon intracellular pH, sodium and contraction in sheep cardiac Purkinje fibres.
    J Physiol. 1988 Apr;398:341-60 PMID: 3392677
  16. Determination of buffering capacity of rat myocardium during ischemia.
    Biochim Biophys Acta. 1988 Aug 19;971(1):9-20 PMID: 2841984
  17. pH regulation in single glomerular mesangial cells. I. Acid extrusion in absence and presence of HCO3-.
    Am J Physiol. 1988 Dec;255(6 Pt 1):C844-56 PMID: 2849306
  18. Regulation of intracellular pH in cardiac muscle.
    Ciba Found Symp. 1988;139:23-46 PMID: 2849528
  19. Movement of acid equivalents across the mammalian smooth muscle cell membrane.
    Ciba Found Symp. 1988;139:3-22 PMID: 2849529
  20. Sodium-hydrogen exchange and its role in controlling contractility during acidosis in cardiac muscle.
    Mol Cell Biochem. 1989 Sep 7;89(2):157-62 PMID: 2554122
  21. The intrinsic intracellular H+ buffering power of snail neurones.
    J Physiol. 1989 Feb;409:89-101 PMID: 2585301
  22. The effects of metabolic inhibition on intracellular calcium and pH in isolated rat ventricular cells.
    J Physiol. 1989 Apr;411:393-418 PMID: 2614727
  23. Comparison of intracellular pH transients in single ventricular myocytes and isolated ventricular muscle of guinea-pig.
    J Physiol. 1990 May;424:343-65 PMID: 2167972
  24. In vivo CO-2 buffer curves of skeletal and cardiac muscle.
    Am J Physiol. 1966 Dec;211(6):1309-12 PMID: 5956541
  25. Reduction of potassium permeability by chloride substitution in cardiac cells.
    J Physiol. 1977 Feb;265(1):193-206 PMID: 850161
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1990-06-00
Pages
429-48
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1189857
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com