EFFECTS OF LACTACIDOSIS ON GLIAL-CELL VOLUME AND VIABILITY

被引:143
作者
STAUB, F
BAETHMANN, A
PETERS, J
WEIGT, H
KEMPSKI, O
机构
[1] Inst. Chirurgische Forschung, Klinikum Grosshadern, 8000 Munchen 70
关键词
Astrocytes; C6; glioma; Cell swelling; Cell viability; Lactacidosis; Na[!sup]+[!/sup]/H[!sup]+[!/sup] antiporter;
D O I
10.1038/jcbfm.1990.143
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Effects of severe lactacidosis were analyzed in vitro by employment of C6 glioma cells and astrocytes from primary culture. The cells were suspended in a physiological medium, which was rendered acidotic by addition of lactic acid in rising concentrations. A pH range of 7.4-4.2 was studied under maintenance of isotonicity and a normal electrolyte concentration of the medium. Cell swelling was quantified by flow cytometry using an advanced Coulter system with hydrodynamic focusing. The method was also utilized for assessment of cell viability by exclusion of the fluorescent dye propidium iodide. The volume of C6 glioma cells was found to increase if the pH was titrated to pH 6.8 or below. From this level downward, the extent of cell swelling depended on the degree of acidosis and the duration of exposure. For example, lactacidosis of pH 6.2 for 60 min led to an increase in cell size to 124.5% of normal, while pH 5.0 or 4.2 led to a cell size of 151.1 or 190.9%, respectively. A comparative analysis of the acidosis-induced cell swelling was made by using sulfuric acid. Swelling of C6 glioma at a given pH was only half of what was found when using lactic acid. This indicates specific swelling-inducing properties of lactic acid, while cell viability was not differently affected by both acids. Of the C6 glioma cells, 89.1% were viable under control conditions at pH 7.4. The viability remained unchanged down to pH 6.2. At pH 5.6, viability remained normal for 30 min, but it decreased to 73.4% after 60 min. Further lowering of pH to 5.0 or 4.6 respectively, decreased the number of viable cells to 47.8 or 40.3%. At pH 4.2 only 21.1% of the cells were surviving 1 h of lactacidosis. Cell swelling from lactacidosis could be largely inhibited by replacement of Na+ and bicarbonate ions in the medium of choline chloride and N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid buffer, suggesting an involvement of the Na+/H+ and Cl-/HCO3- antiporters in the swelling process. Omission of Na+ and bicarbonate was, however, associated with reduced viability of the glial cells in acidosis. The swelling response of astrocytes obtained from primary culture was similar to that of C6 glioma. Lactic acid was also more effective in inducing cell swelling than sulfuric acid at the same level of acidosis. In astrocytes, viability at, e.g., pH 5.6 appeared to be more affected by lactic than by sulfuric acid. Taken together, the current results demonstrate thresholds of acidosis, which are associated with either cell swelling or cell death. Cell swelling was induced from pH 6.8 downward, whereas cell viability started to decline at pH 5.6. Since increasing levels of acidosis were associated with an increasing degree of glial swelling, which resulted, at least in part, from an exchange of intracellular H+ ions against extracellular Na+ ions, the swelling response may be interpreted as a protective mechanism, which was activated to maintain or reestablish a normal intracellular pH, thereby mitigating cell damage from acidosis.
引用
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页码:866 / 876
页数:11
相关论文
共 51 条
  • [1] PATHO-PHYSIOLOGY OF ISCHEMIC CELL-DEATH .1. TIME OF ONSET OF IRREVERSIBLE DAMAGE - IMPORTANCE OF THE DIFFERENT COMPONENTS OF THE ISCHEMIC INSULT
    AMES, A
    NESBETT, FB
    [J]. STROKE, 1983, 14 (02) : 219 - 226
  • [2] EFFECT OF POSTTRAUMATIC HYPOVENTILATION ON CEREBRAL ENERGY-METABOLISM
    ANDERSEN, BJ
    UNTERBERG, AW
    CLARKE, GD
    MARMAROU, A
    [J]. JOURNAL OF NEUROSURGERY, 1988, 68 (04) : 601 - 607
  • [3] THRESHOLDS IN CEREBRAL-ISCHEMIA - THE ISCHEMIC PENUMBRA
    ASTRUP, J
    SIESJO, BK
    SYMON, L
    [J]. STROKE, 1981, 12 (06) : 723 - 725
  • [4] BAETHMAN A, 1978, NEUROSURG REV, V1, P85
  • [5] MEDIATORS OF BRAIN EDEMA AND SECONDARY BRAIN-DAMAGE
    BAETHMANN, A
    MAIERHAUFF, K
    KEMPSKI, O
    UNTERBERG, A
    WAHL, M
    SCHURER, L
    [J]. CRITICAL CARE MEDICINE, 1988, 16 (10) : 972 - 978
  • [6] RELEASE OF GLUTAMATE AND OF FREE FATTY-ACIDS IN VASOGENIC BRAIN EDEMA
    BAETHMANN, A
    MAIERHAUFF, K
    SCHURER, L
    LANGE, M
    GUGGENBICHLER, C
    VOGT, W
    JACOB, K
    KEMPSKI, O
    [J]. JOURNAL OF NEUROSURGERY, 1989, 70 (04) : 578 - 591
  • [7] TRANSPORT OF H+ AND OF IONIC WEAK ACIDS AND BASES
    BORON, WF
    [J]. JOURNAL OF MEMBRANE BIOLOGY, 1983, 72 (1-2) : 1 - 16
  • [8] CHAUSSY L, 1981, CEREBRAL MICROCIRCUL, P29
  • [9] CHOI DW, 1987, BRAIN RES, V403, P33
  • [10] Crissman HA., 1979, FLOW CYTOMETRY SORTI, P243