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Meeting Abstracts  |   May 1996
Volatile Anesthetics Selectively Inhibit the Calcium sup 2+ -transporting ATPase in Neuronal and Erythrocyte Plasma Membranes
Author Notes
  • (Fomitcheva) Postdoctoral Fellow.
  • (Kosk-Kosicka) Associate Professor of Anesthesiology and Biological Chemistry.
  • Received from the Department of Anesthesiology and Critical Care Medicine, The Johns Hopkins University, School of Medicine, Baltimore, Maryland. Submitted for publication June 23, 1995. Accepted for publication January 5, 1996. Supported by grant GM 447130 from the National Institutes of Health and a Grant-in-Aid from the National American Heart Association. Presented in part at the annual meeting of the Biophysical Society, New Orleans, Louisiana, March 6-10, 1994; the annual meeting of American Society of Anesthesiologists, San Francisco, California, October 15-19, 1994; and the International Workshop on Anesthetic Mechanisms, Takamatsu, Japan, December 12-14, 1994.
  • Address reprint requests to Dr. Kosk-Kosicka: Department of Anesthesiology and Critical Care Medicine, The Johns Hopkins University, 600 North Wolfe Street, Blalock 1404-C, Baltimore, Maryland 21287-4961.
Article Information
Meeting Abstracts   |   May 1996
Volatile Anesthetics Selectively Inhibit the Calcium sup 2+ -transporting ATPase in Neuronal and Erythrocyte Plasma Membranes
Anesthesiology 5 1996, Vol.84, 1189-1195. doi:
Anesthesiology 5 1996, Vol.84, 1189-1195. doi:
Key words: Anesthetics, intravenous: sodium pentobarbital. Anesthetics, volatile: halothane; isoflurane. Cell: erythrocyte; synaptosomal membranes. Enzymes, Calcium2+ -transporting ATPase, Calcium2+ -ATPase, Sodium sup +, Potassium sup + -ATPase, Magnesium2+ -ATPase: enzyme inactivation. Ions, calcium: cell Calcium2+ homeostasis.
THE PMCA (plasma membrane Calcium2+ -transporting adenosine triphosphatase [ATPase] 3.6.1.38) of human erythrocytes has been demonstrated to be a suitable model for investigation of the mechanism of action of volatile anesthetics on an integral membrane protein. [1,2] In human erythrocytes that lack voltage-sensitive and ligand-gated Calcium sup 2+ channels, Sodium sup +/Calcium2+ exchanger, or an intracellular membrane Calcium2+ -transporting ATPase, PMCA is the sole Calcium2+ -transporting entity. In other cells, where the aforementioned systems coexist and cooperate in regulating intracellular Calcium2+, PMCA has a specific role in fine-tuning Calcium2+ levels, that is, continuously maintain Calcium2+ below high nanomolar concentrations because it is the system with the highest affinity for Calcium2+ (K1/2 = 90-260 nM Ca2+, as determined for the purified red cell PMCA). [3] Subsequently, it was reported that the PMCA of synaptosomal plasma membranes where various Calcium2+ -transporting systems are present also is inhibited by the anesthetics. [4-6] This inhibition is not limited to the halogenated volatile anesthetics but also is shown by xenon and nitrous oxide. [6,7] The finding that PMCA activity is altered by the anesthetics at their clinical concentrations opens a possibility that the enzyme might be affected during anesthesia. The consequences could be multiple because so many cellular events and cascades depend on precisely controlled intracellular Calcium2+ concentrations, ranging from regulation of cell shape in red blood cells to synaptic transmission. Among the systems activated by high nanomolar neuronal free Calcium2+ (above 100 nM) concentrations are calmodulin, protein kinase C, phospholipase A2, and calpain. [8] Excessive activation of any of them would affect neuronal functions.
The purpose of the current study was to determine the selectivity of the observed inhibition. In particular, we determined whether the impairment of enzymatic function is unique to the PMCA and this particular group of general anesthetics. Furthermore, the effects were investigated simultaneously on synaptosomal membranes and red blood cell membranes to establish whether the PMCA of neuronal cells has the same sensitivity to both groups of general anesthetics, volatile anesthetics and barbiturates, as the well-characterized enzyme of erythrocytes, which is solely responsible for maintaining intracellular Calcium2+ homeostasis.
Materials and Methods
Thymol-free halothane was obtained from Halcarbon Laboratories (River Edge, NJ), isoflurane was purchased from Anaquest (Liberty Corner, NJ), and sodium pentobarbital was purchased from Anpro Pharmaceutical (Arcadia, CA).
The methods used for preparation of erythrocyte membranes and determination of protein and Calcium2+ concentrations were described previously. [3,9] Briefly, the membranes were prepared in hypotonic solutions from outdated human red blood cells purchased from the local Red Cross. The erythrocytes were lysed and washed several times in the presence of ethylenediamenetetraacetic acid to remove endogenous calmodulin. Ethylenediamenetetraacetic acid was subsequently removed by several washes with Tris buffer. Synaptosomal membranes were prepared from cerebellar lobes purchased from Pel-freez Biologicals (Rogers, AR), which were isolated from Sprague-Dawley rats and frozen in liquid nitrogen within 2 min after the animals were killed. Synaptosomal membranes were prepared by Dr. Zylinska [4,5] by the method of Booth and Clark [10] using Ficoll gradient centrifugation, as described previously. [11,12] Plasma membranes were the dominant component, as determined previously by electron microscopy [11] and marker enzyme activity assays. No endoplasmic reticulum membranes were present as evidenced by lack of any inhibitory effect of thapsigargin at concentrations up to 1 micro Meter. Mitochondrial membranes' contamination was less than 10%, as determined in the presence of specific inhibitors of mitochondrial activities, oligomycin (0.5-2 micro gram/ml) and sodium azide (1 mM). We have established that PMCA of both red blood cells (RBC) and synaptosomal membrane (SM) preparations had similar sensitivity to volatile anesthetics in the presence and absence of calmodulin. Thus, we have decided to routinely use SM preparations that were not totally depleted of calmodulin to avoid a considerable loss of material owing to the extensive ethylenediamenetetraacetic acid washes. The activity assays were normally performed in the absence of exogenous calmodulin except for the assays of barbiturate effects on PMCA in RBC in which 6 nM calmodulin was added to provide stimulation of PMCA activity comparable to that of the enzyme in SM.
Adenosine triphosphatase activities were determined by measurements of inorganic phosphate production, as described previously for the Calcium2+ -ATPase activity of PMCA in RBC. [1] The activity was assayed in the reaction mixture containing 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, 17.5 micro Meter free Calcium2+, and 3 mM adenosine triphosphate. The activity was calculated as a difference between the activity determined in the above reaction mixture and the reaction mixture in which Calcium2+ was omitted. The PMCA activity was sensitive to orthovanadate.
The ATPase activities not related to PMCA were studied in the presence of the following ions in the reaction mixture just described: (1) Magnesium2+ -ATPase at 8 mM Magnesium2+ (no Calcium2+); (2) Calcium2+ -ATPase at 8 mM Calcium2+ (no Magnesium2+); (3) Sodium sup +, Potassium sup + -ATPase at 15 mM Potassium sup + and 130 mM Sodium sup + (no Calcium2+), in the presence and absence of ouabain. The Sodium sup +, Potassium sup + -ATPase activity was calculated as the activity inhibited by 1 mM ouabain. All other assay conditions were the same as for the PMCA. Activity of the Magnesium2+ -ATPase and Calcium sup 2+ -ATPase was resistant to orthovanadate, the selective inhibitor of ion-transporting ATPases. [13] .
The assays were performed in sealed 0.65-ml polypropylene tubes in a total reaction volume of 330 micro liter. The anesthetics were added after the addition of all reagents and membrane preparations, immediately before starting the reaction with adenosine triphosphate. Halothane and isoflurane were delivered to the reaction tube in an airtight Hamilton syringe from saturated solutions in reaction mixture. The assay was performed at 37 degrees C. Aliquots were withdrawn at 15-30 min for colorimetric inorganic phosphate measurement. Steady-state velocities were obtained from plots of inorganic phosphate production that were linear with time.
In parallel to the activity assay, tubes were incubated under identical conditions and used for determination of the effective halothane concentrations during the activity assay. The anesthetic was extracted with heptane, measured by gas chromatography, and the concentrations were calculated as described earlier. [1] .
Standard deviations (SD) and standard errors were used to compare groups of data. Data are expressed as the mean+/-SEM of independent experiments performed in triplicates.
Protein concentration was measured using the BioRad protein microassay (Hercules, CA). Total calcium was measured by atomic absorption, and free Calcium2+ concentrations were calculated based on the constants given by Schwartzenbach et al. [14] .
Results
(Figure 1) shows specific activities of several ATPases that are integral protein constituents of SM and RBC plasma membranes. Four activities have been determined in the synaptosomal membranes of which the Sodium sup +, Potassium sup + -ATPase was the highest (2), followed by PMCA (1), and Magnesium2+ -ATPase (3). In addition, there was a Calcium2+ -ATPase activity (4) that in contrast to PMCA did not require Magnesium2+ and was not involved in Calcium2+ transport. It was very similar to the Magnesium2+ -ATPase activity in accordance with the possibility that the two activities may represent the same enzyme. [15,16] . This Calcium2+ -ATPase was insensitive to orthovanadate in contrast to the PMCA, which was totally inhibited by 0.1 mM orthovanadate. At 0.1 mM orthovanadate, the Magnesium2+ -ATPase was inhibited by only 20%, indicating that only a small part of the activity pertains to a P-type Magnesium2+ -ATPase.
Figure 1. Adenosine triphosphatase (ATPase) activities in synaptosomal membranes and red blood cell membranes: plasma membrane Calcium2+ -transporting adenosine triphosphatase (PMCA; open square), Sodium sup +, Potassium sup + -ATPase (*symbol*), Magnesium2+ -ATPase (*symbol*), and Calcium2+ -ATPase (*symbol*). Preparations of plasma membranes and activity assays were done as described in materials and methods. The "basic" reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, and 3 mM ATP. In addition, the following ions were included in the assays as required for particular ATPase activities: (1) PMCA: 17.5 micro Meter free Calcium2+; (2) Sodium sup +, Potassium sup + -ATPase: 15 mM Potassium sup + and 130 mM Sodium sup +; (3) Magnesium2+ -ATPase: none; (2) Calcium2+ -ATPase: 8 mM Calcium2+ (Magnesium2+ omitted). Ouabain, a selective inhibitor of the Sodium sup +, Potassium sup + -pump was 1 mM. Protein concentration was 100-120 micro gram red blood cells and 10-15 micro gram synaptosomal membranes per one milliliter. Total reaction volume was 100 micro liter. The error bars indicate SEM of replicates; the number of experiments was 4-9.
Figure 1. Adenosine triphosphatase (ATPase) activities in synaptosomal membranes and red blood cell membranes: plasma membrane Calcium2+ -transporting adenosine triphosphatase (PMCA; open square), Sodium sup +, Potassium sup + -ATPase (*symbol*), Magnesium2+ -ATPase (*symbol*), and Calcium2+ -ATPase (*symbol*). Preparations of plasma membranes and activity assays were done as described in materials and methods. The "basic" reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, and 3 mM ATP. In addition, the following ions were included in the assays as required for particular ATPase activities: (1) PMCA: 17.5 micro Meter free Calcium2+; (2) Sodium sup +, Potassium sup + -ATPase: 15 mM Potassium sup + and 130 mM Sodium sup +; (3) Magnesium2+ -ATPase: none; (2) Calcium2+ -ATPase: 8 mM Calcium2+ (Magnesium2+ omitted). Ouabain, a selective inhibitor of the Sodium sup +, Potassium sup + -pump was 1 mM. Protein concentration was 100-120 micro gram red blood cells and 10-15 micro gram synaptosomal membranes per one milliliter. Total reaction volume was 100 micro liter. The error bars indicate SEM of replicates; the number of experiments was 4-9.
Figure 1. Adenosine triphosphatase (ATPase) activities in synaptosomal membranes and red blood cell membranes: plasma membrane Calcium2+ -transporting adenosine triphosphatase (PMCA; open square), Sodium sup +, Potassium sup + -ATPase (*symbol*), Magnesium2+ -ATPase (*symbol*), and Calcium2+ -ATPase (*symbol*). Preparations of plasma membranes and activity assays were done as described in materials and methods. The "basic" reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, and 3 mM ATP. In addition, the following ions were included in the assays as required for particular ATPase activities: (1) PMCA: 17.5 micro Meter free Calcium2+; (2) Sodium sup +, Potassium sup + -ATPase: 15 mM Potassium sup + and 130 mM Sodium sup +; (3) Magnesium2+ -ATPase: none; (2) Calcium2+ -ATPase: 8 mM Calcium2+ (Magnesium2+ omitted). Ouabain, a selective inhibitor of the Sodium sup +, Potassium sup + -pump was 1 mM. Protein concentration was 100-120 micro gram red blood cells and 10-15 micro gram synaptosomal membranes per one milliliter. Total reaction volume was 100 micro liter. The error bars indicate SEM of replicates; the number of experiments was 4-9.
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As compared to SM, in RBCs, all ATPase activities were significantly lower. For example, the activity of PMCA was 1.0+/- 0.25 as compared to 31+/-4.5 micro mol Pi/mg protein/h in SM. Furthermore, in contrast to SM in erythrocytes, the PMCA activity was dominant whereas the Sodium sup +, Potassium sup + -ATPase was very low (0.50+/-0.18), in the same range as the Magnesium2+ -ATPase (0.38+/-0.06 micro mol Pi/mg/h). The orthovanadate-insensitive Calcium2+ -ATPase activity was not detectable in erythrocyte membranes.
The Effect of Volatile Anesthetics on Adenosine Triphosphatase Activities in Synaptosomal Membranes and Erythrocytes
As shown previously, [1] increasing concentrations of halothane reduced the PMCA activity in erythrocytes. Figure 2demonstrates that halothane also reduce the PMCA activity in synaptosomal membranes. This inhibition was comparable to that of erythrocyte enzyme: it was dose-dependent and occured at anesthetic concentrations of halothane (Table 1). Also, the effects of isoflurane (Figure 3and Table 1) on the PMCA activity were comparable in the two membranes.
Figure 2. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by halothane. The enzyme activity was assayed as described in materials and methods and the legend to Figure 1. The reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, 17.5 micro Meter free Calcium2+, and 3 mM ATP. The activity was calculated as a difference between the activity determined in the above reaction mixture and the reaction mixture in which Calcium2+ was omitted. The activity was sensitive to orthovanadate. As shown in Figure 1, 100% was the maximal activity determined for each membrane (31.5+/-4.5 and 1.0 +/-0.25 micro molPi/mg protein/h for synaptosomal membranes and red blood cell membranes, respectively). The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 2. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by halothane. The enzyme activity was assayed as described in materials and methods and the legend to Figure 1. The reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, 17.5 micro Meter free Calcium2+, and 3 mM ATP. The activity was calculated as a difference between the activity determined in the above reaction mixture and the reaction mixture in which Calcium2+ was omitted. The activity was sensitive to orthovanadate. As shown in Figure 1, 100% was the maximal activity determined for each membrane (31.5+/-4.5 and 1.0 +/-0.25 micro molPi/mg protein/h for synaptosomal membranes and red blood cell membranes, respectively). The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 2. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by halothane. The enzyme activity was assayed as described in materials and methods and the legend to Figure 1. The reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, 17.5 micro Meter free Calcium2+, and 3 mM ATP. The activity was calculated as a difference between the activity determined in the above reaction mixture and the reaction mixture in which Calcium2+ was omitted. The activity was sensitive to orthovanadate. As shown in Figure 1, 100% was the maximal activity determined for each membrane (31.5+/-4.5 and 1.0 +/-0.25 micro molPi/mg protein/h for synaptosomal membranes and red blood cell membranes, respectively). The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
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Table 1. Comparison of Clinical (EC50) and Inhibitory (I50) Potencies of Anesthetics
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Table 1. Comparison of Clinical (EC50) and Inhibitory (I50) Potencies of Anesthetics
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Figure 3. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by isoflurane. The activity was assayed as described in materials and methods and the legend to Figure 2. One hundred percent is the maximal activity determined for each membrane, as shown in Figure 1. The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 3. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by isoflurane. The activity was assayed as described in materials and methods and the legend to Figure 2. One hundred percent is the maximal activity determined for each membrane, as shown in Figure 1. The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 3. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by isoflurane. The activity was assayed as described in materials and methods and the legend to Figure 2. One hundred percent is the maximal activity determined for each membrane, as shown in Figure 1. The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
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The effects of halothane and isoflurane on PMCA activity were subsequently compared to their effects on the other ATPase activities present in plasma membranes. Figure 4shows the data for halothane in synaptosomal membranes. Twofold to threefold higher anesthetic concentrations were required to half-maximally inhibit the Sodium sup +, Potassium sup + -ATPase as compared to the PMCA. At the highest halothane concentrations studied, the Magnesium2+ -ATPase activity was inhibited by only [nearly equal] 30%. The inhibition pattern of the Calcium2+ -ATPase activity closely resembled that of the Magnesium sup 2+ -ATPase, in line with the possibility that the two activities represented the same enzyme.
Figure 4. Comparison of halothane effects on various ATPase activities in synaptosomal membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), Magnesium2+ -ATPase (closed circle), and Calcium2+ -ATPase ([diamond]) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of halothane (Figure 1). Values represent means of triplicate measurements of two to four experiments for each enzyme.
Figure 4. Comparison of halothane effects on various ATPase activities in synaptosomal membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), Magnesium2+ -ATPase (closed circle), and Calcium2+ -ATPase ([diamond]) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of halothane (Figure 1). Values represent means of triplicate measurements of two to four experiments for each enzyme.
Figure 4. Comparison of halothane effects on various ATPase activities in synaptosomal membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), Magnesium2+ -ATPase (closed circle), and Calcium2+ -ATPase ([diamond]) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of halothane (Figure 1). Values represent means of triplicate measurements of two to four experiments for each enzyme.
×
(Figure 5) compares activity patterns of the three enzymes in erythrocyte membranes in the presence of isoflurane. Similar to the SM, also in erythrocytes, PMCA activity was distinctly more sensitive to the anesthetic than the activities of Sodium sup +, Potassium sup + -ATPase and Magnesium2+ -ATPase.
Figure 5. Comparison of isoflurane effects on ATPase activities in red blood cell membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 4.
Figure 5. Comparison of isoflurane effects on ATPase activities in red blood cell membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 4.
Figure 5. Comparison of isoflurane effects on ATPase activities in red blood cell membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 4.
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The Effect of Sodium Pentobarbital on Adenosine Triphosphatase Activities in Synaptosomal Membranes and Erythrocytes
(Figure 6) shows effects of sodium pentobarbital on ATPase activities in SM. None of the enzymes were inhibited at anesthetic concentrations of the barbiturate, i.e., 50-100 micro meter [17,18] (Figure 6and Table 1). At higher concentrations, dose-dependent effects were observed: the half-maximal inhibition of the PMCA activity occurred at 11 mM pentobarbital, comparable to the Sodium sup +, Potassium sup + -ATPase. The Magnesium2+ -ATPase activity was half maximally inhibited at I sub 50 = 16-17 mM barbiturate concentration.
Figure 6. Inhibition of ATPase activities in synaptosomal membranes by sodium pentobarbital. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of the barbiturate (Figure 1). Values represent means of triplicate measurements of 2-4 experiments for each enzyme.
Figure 6. Inhibition of ATPase activities in synaptosomal membranes by sodium pentobarbital. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of the barbiturate (Figure 1). Values represent means of triplicate measurements of 2-4 experiments for each enzyme.
Figure 6. Inhibition of ATPase activities in synaptosomal membranes by sodium pentobarbital. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of the barbiturate (Figure 1). Values represent means of triplicate measurements of 2-4 experiments for each enzyme.
×
Similar inhibition patterns also were demonstrated for the three ATPase activities in red cell membranes, with an I50of 10-11 mM for PMCA (Table 1), 17 mM for the Sodium sup +, Potassium sup + - ATPase, and I50> 20 mM for the Magnesium2+ -ATPase. [19] .
Discussion
The PMCA of neuronal cells shows the same sensitivity to halogenated volatile anesthetics as the PMCA of erythrocytes. Both are inhibited in a dose-dependent manner at clinical anesthetic concentrations, with the half-maximal effect observed at [nearly equal] 1 minimum alveolar concentration of either halothane or isoflurane. Furthermore, also the Calcium2+ -transport ATPase in endothelial cells of cerebral microvessels has a comparable sensitivity to these anesthetics. [5] The data suggest that independent of the cell type, its specific PMCA activity, and expected differences in its lipid composition and membrane asymmetry, the PMCA is similarly affected by volatile anesthetics in vitro. In line with these observations also is the similarity of the sensitivity to the anesthetics of the Calcium2+ -transporting ATPase purified from either RBC or SM, which is twofold higher than that of the enzyme in the membranes. [1,20] This is an interesting finding because the PMCA of the three plasma membranes may significantly differ in its isoform composition, as indicated by tissue distribution of four PMCA isoforms to which antibodies were raised. [21,22] Isoforms 1 and 4 are expressed in all analyzed human and rat tissues. Whereas RBC contain only PMCA 1 and 4, neuronal tissues have in addition isoforms 2 and 3, with PMCA 2 present specifically in high concentration in cerebellum. Thus, it appears that all PMCA isoforms have similar sensitivity to volatile anesthetics. This would be in agreement with an impairment introduced by anesthetic binding in PMCA domains shared by all isoforms.
Activities of other ATPases that have been studied in the same membrane preparations and under comparable conditions are significantly less sensitive to volatile anesthetics. The relatively low sensitivity of the Sodium sup +, Potassium sup + -ATPase, which together with the PMCA belongs to the ion-transporting P-type ATPases, is in agreement with previous reports. [23,7] The other two ATPase activities are inhibited by volatile anesthetics by only 30% at the maximal studied anesthetic concentrations that totally inhibit the PMCA. Of these two activities in synaptosomal membranes, only 20% of the Magnesium2+ -ATPase activity pertains to a P-type ATPase, as indicated by its response to orthovanadate, a specific inhibitor of this class of ATPases. The Calcium sup 2+ -ATPase activity (unrelated to PMCA) in SM, which is totally resistant to orthovanadate, represents most probably an ecto-ATPase, described by several laboratories, which also may be stimulated by Magnesium2+. [15,24] (This would be in agreement with the finding that 80% of Magnesium2+ -ATPase activity in our membrane preparation is not inhibited by orthovanadate). Similar inhibition of the vanadate-insensitive ecto-ATPase activity ([nearly equal] 40%) was observed in a different preparation of rat brain synaptic plasma membranes at 1.5 vol% halothane. [6] In summary, the PMCA is significantly more sensitive to volatile anesthetics than other ATPases studied in the same membrane. In addition, it is more sensitive than an intracellular membrane Calcium2+ -transporting ATPase of SR of both skeletal and cardiac muscle. [25-28] .
In contrast to volatile anesthetics, the inhibition caused by barbiturates cannot be regarded as either selective or relevant to their pharmacologic action. Sodium pentobarbital at its clinical concentrations does not inhibit the PMCA studied in either of the two plasma membranes (present study) or in a purified form. [19] Furthermore, the differences in the sensitivity of various ATPases to the barbiturate at supraclinical concentrations are small as compared to volatile anesthetics.
Comparison of the effects of the representatives of the two groups of general anesthetics on the PMCA of different cell types (current report) and on the purified enzyme [19,25] suggests different sites for their action on the PMCA molecule. We have previously [25] proposed that volatile anesthetics permeate enzyme molecules and interact with nonpolar sites (cavities) in the interior, as has been demonstrated earlier for hemoglobin and myoglobin by nuclear magnetic resonance spectroscopy and X-ray crystallography studies. [28,29] Such an interaction is expected to modify conformational substrates of the enzyme and impair its function as shown by anesthetic-induced conformational changes that could result in impaired Calcium2+ binding to the enzyme and loss of its activity. [25] In contrast, it is postulated that barbiturates inhibit the PMCA by binding to the exposed nonpolar patch on enzyme surface that is involved in enzyme activation. [19] This less selective binding would result in a similar overall effect (inhibition of enzyme activity) as with volatile anesthetics, however, at distinctly higher drug concentrations. The molecular events leading from the binding to inhibition of enzyme activity are expected to be different for barbiturates and volatile anesthetics, as suggested for example by twofold to threefold stronger effects of barbiturates on calmodulin-activated PMCA monomers than dimers in contrast to equal concentration dependence observed with volatile anesthetics. [1,19] .
The comparative approach allowed us to establish that the inhibition of PMCA by volatile anesthetics in vitro is selective by the following criteria. (1) None of the other ATPases studied are significantly inhibited by volatile anesthetics at 1 or 2 minimum alveolar concentrations, as is the PMCA. (2) Barbiturates do not inhibit the PMCA at their clinical concentrations. (3) The PMCA in the two plasma membranes responds very similarly: it shows the same difference in sensitivity to volatile anesthetics versus to pentobarbital and is significantly more sensitive to the volatile anesthetics than the other enzymes studied.
REFERENCES
Kosk-Kosicka D, Roszczynska G: Inhibition of plasma membrane Calcium sup 2+ -ATPase activity by volatile anesthetics. ANESTHESIOLOGY 1993; 79:774-80.
Kosk-Kosicka D: Plasma membrane Calcium sup 2+ -ATPase as a target for volatile anesthetics. Adv Pharmacol 1994; 31:313-22.
Kosk-Kosicka D, Bzdega T, Johnson JD: Fluorescence studies on calmodulin binding to erythrocyte Calcium sup 2+ -ATPase in different oligomerization states. Biochemistry 1990; 29:1875-9.
Roszczynska G, Zylinska L, Kosk-Kosicka D: Similar inhibitory effect of halothane on the function of the Calcium sup 2+ -ATPase from cerebellum and erythrocytes (abstract). Biophys J 1994; 66:119.
Kosk-Kosicka D, Fomitcheva I, Zylinska L, Hurn PD, Traystman RJ, Roszczynska: Plasma membrane Magnesium sup 2+, Calcium sup 2+ -ATPase from three tissues is inhibited by volatile anesthetics at clinically relevant concentrations. Progr Anesth Mech 1995; 3:279-83.
Franks JJ, Horn J-L, Janicki PK, Singh G: Halothane, isoflurane, xenon, and nitrous oxide inhibit calcium ATPase pump activity in rat brain synaptic plasma membranes. ANESTHESIOLOGY 1995; 82:108-17.
Franks JJ, Horn J-L, Janicki PK, Singh G: Stable inhibition of brain synaptic plasma membrane calcium ATPase in rats anesthetized with halothane. ANESTHESIOLOGY 1995; 82:118-28.
Wang KKW, Yuen P-W: Calpain inhibition: An overview of its therapeutic potential. Trends Pharmacol Sci 1994; 15:412-9.
Kosk-Kosicka D, Bzdega T: Activation of the erythrocyte Calcium sup 2+ -ATPase by either self association or interaction with calmodulin. J Biol Chem 1988; 263:18184-9.
Booth RFG, Clark JB: A rapid method for the preparation of relatively pure metabolically competent synaptosomes from rat brain. Biochem J 1978; 176:365-70.
Szkudlarek J, Lachowicz L, Wojtkowiak R: Effects in vitro of L-glutamate and kainic acid on the ATPase activities of synaptosomal membranes from different areas of rat brain. Neurosci Lett 1986; 65:304-10.
Zylinska L, Lachowicz L: Characterization of 130 kDa protein from rat cerebellum synaptosomal membranes phosphorylated by PKC. Int J Biochem 1992; 24:1057-64.
Pedersen PL, Carafoli E: Ion motive ATPases. II. Energy coupling and work output. Trends Biochem Sci 1978; 12:186-9.
Schwartzenbach G, Senn H, Anderegg, G: Komplexone XXIX. Ein grosser Chelateffekt besonderer Art. Helv Chim Acta 1957; 40:1886-1900.
Hohmann J, Kowalewski H, Vogel M, Zimmermann H: Isolation of a Calcium sup 2+ or Magnesium sup 2+ -activated ATPase (ecto-ATPase) from bovine brain synaptic membranes. Biochim Biophys Acta 1993; 1152:146-54.
Sorensen RG, Mahler HR: Calcium-stimulated adenosine triphosphatases in synaptic membranes. J Neurochem 1981; 37:1407-18.
Fisher RS, Walker JT, Plummer CW: Quantitative estimation of barbiturates in blood by ultra-violet spectrophotometry. Am J Pathol 1948; 18:462-9.
Richter JA, Holtman JR Jr: Barbiturates: Their in vivo effects and potential biochemical mechanisms. Prog Neurobiol 1982; 18:275-319.
Kosk-Kosicka D, Fomitcheva I, Lopez MM: Mechanism of inhibition of the plasma membrane Calcium sup 2+ -ATPase by barbiturates. Biochemistry 1996; 35:900-5.
Kosk-Kosicka D, Fomitcheva I, Zylinska L: Similar inhibitory effects of volatile anesthetics on the function of the Calcium sup 2+ -ATPase from erythrocyte and synaptosomal membranes (abstract). ANESTHESIOLOGY 1994; 81:A902.
Stauffer TP, Guerini D, Carafoli E: Tissue distribution of the four gene products of the plasma membrane Calcium sup 2+ pump. J Biol Chem 1995; 270:12184-90.
Carafoli E: Biogenesis: Plasma membrane calcium ATPase: 15 years of work on the purified enzyme. FASEB J 1994; 8:903-1002.
Ueda I, Mietani W: Microsomal ATPase of rabbit brain and effects of general anesthetics. Biochem Pharmacol 1967; 16:1370-4.
Nagy AK, Shuster TA, Delgado-Escueta A: Ecto-ATPase of mammalian synaptosomes: identification and enzymic characterization. J Neurochem 1986; 47:976-86.
Lopez MM, Kosk-Kosicka D: How do volatile anesthetics inhibit Calcium sup 2+ -ATPases? J Biol Chem 1995; 270:28239-45.
Karon BS, Thomas DD: Molecular mechanism of Ca-ATPase activation by halothane in sarcoplasmic reticulum. Biochemistry 1993; 32:7503-11.
Miao N, Frazer MJ, Lynch CIII: Anesthetic actions on calcium uptake and calcium-dependent adenosine triphosphatase activity of cardiac sarcoplasmic reticulum. Adv Pharmacol 1994; 31:145-65.
Schoenborn BP, Featherstone RM: Molecular Forces in Anesthesia, Advances in Pharmacology. New York, Academic, 1967, pp 1-17.
Tilton RF, Kuntz ID, Petsko GA: Cavities in proteins: Structure of a metmyoglobin-xenon complex solved to 1.9 A. Biochemistry 1984; 23:2849-57.
Franks NP, Lieb WR: Molecular and cellular mechanisms of general anesthesia. Nature 1994; 367:607-14.
Figure 1. Adenosine triphosphatase (ATPase) activities in synaptosomal membranes and red blood cell membranes: plasma membrane Calcium2+ -transporting adenosine triphosphatase (PMCA; open square), Sodium sup +, Potassium sup + -ATPase (*symbol*), Magnesium2+ -ATPase (*symbol*), and Calcium2+ -ATPase (*symbol*). Preparations of plasma membranes and activity assays were done as described in materials and methods. The "basic" reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, and 3 mM ATP. In addition, the following ions were included in the assays as required for particular ATPase activities: (1) PMCA: 17.5 micro Meter free Calcium2+; (2) Sodium sup +, Potassium sup + -ATPase: 15 mM Potassium sup + and 130 mM Sodium sup +; (3) Magnesium2+ -ATPase: none; (2) Calcium2+ -ATPase: 8 mM Calcium2+ (Magnesium2+ omitted). Ouabain, a selective inhibitor of the Sodium sup +, Potassium sup + -pump was 1 mM. Protein concentration was 100-120 micro gram red blood cells and 10-15 micro gram synaptosomal membranes per one milliliter. Total reaction volume was 100 micro liter. The error bars indicate SEM of replicates; the number of experiments was 4-9.
Figure 1. Adenosine triphosphatase (ATPase) activities in synaptosomal membranes and red blood cell membranes: plasma membrane Calcium2+ -transporting adenosine triphosphatase (PMCA; open square), Sodium sup +, Potassium sup + -ATPase (*symbol*), Magnesium2+ -ATPase (*symbol*), and Calcium2+ -ATPase (*symbol*). Preparations of plasma membranes and activity assays were done as described in materials and methods. The "basic" reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, and 3 mM ATP. In addition, the following ions were included in the assays as required for particular ATPase activities: (1) PMCA: 17.5 micro Meter free Calcium2+; (2) Sodium sup +, Potassium sup + -ATPase: 15 mM Potassium sup + and 130 mM Sodium sup +; (3) Magnesium2+ -ATPase: none; (2) Calcium2+ -ATPase: 8 mM Calcium2+ (Magnesium2+ omitted). Ouabain, a selective inhibitor of the Sodium sup +, Potassium sup + -pump was 1 mM. Protein concentration was 100-120 micro gram red blood cells and 10-15 micro gram synaptosomal membranes per one milliliter. Total reaction volume was 100 micro liter. The error bars indicate SEM of replicates; the number of experiments was 4-9.
Figure 1. Adenosine triphosphatase (ATPase) activities in synaptosomal membranes and red blood cell membranes: plasma membrane Calcium2+ -transporting adenosine triphosphatase (PMCA; open square), Sodium sup +, Potassium sup + -ATPase (*symbol*), Magnesium2+ -ATPase (*symbol*), and Calcium2+ -ATPase (*symbol*). Preparations of plasma membranes and activity assays were done as described in materials and methods. The "basic" reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, and 3 mM ATP. In addition, the following ions were included in the assays as required for particular ATPase activities: (1) PMCA: 17.5 micro Meter free Calcium2+; (2) Sodium sup +, Potassium sup + -ATPase: 15 mM Potassium sup + and 130 mM Sodium sup +; (3) Magnesium2+ -ATPase: none; (2) Calcium2+ -ATPase: 8 mM Calcium2+ (Magnesium2+ omitted). Ouabain, a selective inhibitor of the Sodium sup +, Potassium sup + -pump was 1 mM. Protein concentration was 100-120 micro gram red blood cells and 10-15 micro gram synaptosomal membranes per one milliliter. Total reaction volume was 100 micro liter. The error bars indicate SEM of replicates; the number of experiments was 4-9.
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Figure 2. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by halothane. The enzyme activity was assayed as described in materials and methods and the legend to Figure 1. The reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, 17.5 micro Meter free Calcium2+, and 3 mM ATP. The activity was calculated as a difference between the activity determined in the above reaction mixture and the reaction mixture in which Calcium2+ was omitted. The activity was sensitive to orthovanadate. As shown in Figure 1, 100% was the maximal activity determined for each membrane (31.5+/-4.5 and 1.0 +/-0.25 micro molPi/mg protein/h for synaptosomal membranes and red blood cell membranes, respectively). The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 2. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by halothane. The enzyme activity was assayed as described in materials and methods and the legend to Figure 1. The reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, 17.5 micro Meter free Calcium2+, and 3 mM ATP. The activity was calculated as a difference between the activity determined in the above reaction mixture and the reaction mixture in which Calcium2+ was omitted. The activity was sensitive to orthovanadate. As shown in Figure 1, 100% was the maximal activity determined for each membrane (31.5+/-4.5 and 1.0 +/-0.25 micro molPi/mg protein/h for synaptosomal membranes and red blood cell membranes, respectively). The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 2. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by halothane. The enzyme activity was assayed as described in materials and methods and the legend to Figure 1. The reaction mixture contained 50 mM Tris-maleate, pH 7.4, 120 mM KCl, 8 mM MgCl2, 1 mM EGTA, 17.5 micro Meter free Calcium2+, and 3 mM ATP. The activity was calculated as a difference between the activity determined in the above reaction mixture and the reaction mixture in which Calcium2+ was omitted. The activity was sensitive to orthovanadate. As shown in Figure 1, 100% was the maximal activity determined for each membrane (31.5+/-4.5 and 1.0 +/-0.25 micro molPi/mg protein/h for synaptosomal membranes and red blood cell membranes, respectively). The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
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Figure 3. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by isoflurane. The activity was assayed as described in materials and methods and the legend to Figure 2. One hundred percent is the maximal activity determined for each membrane, as shown in Figure 1. The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 3. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by isoflurane. The activity was assayed as described in materials and methods and the legend to Figure 2. One hundred percent is the maximal activity determined for each membrane, as shown in Figure 1. The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
Figure 3. Comparison of inhibition of PMCA activity in red blood cell (open triangle) and synaptosomal membranes (closed triangle) by isoflurane. The activity was assayed as described in materials and methods and the legend to Figure 2. One hundred percent is the maximal activity determined for each membrane, as shown in Figure 1. The error bars indicate SEM of replicates, and are shown when their dimensions exceed those of the symbols. Three independent experiments were performed.
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Figure 4. Comparison of halothane effects on various ATPase activities in synaptosomal membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), Magnesium2+ -ATPase (closed circle), and Calcium2+ -ATPase ([diamond]) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of halothane (Figure 1). Values represent means of triplicate measurements of two to four experiments for each enzyme.
Figure 4. Comparison of halothane effects on various ATPase activities in synaptosomal membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), Magnesium2+ -ATPase (closed circle), and Calcium2+ -ATPase ([diamond]) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of halothane (Figure 1). Values represent means of triplicate measurements of two to four experiments for each enzyme.
Figure 4. Comparison of halothane effects on various ATPase activities in synaptosomal membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), Magnesium2+ -ATPase (closed circle), and Calcium2+ -ATPase ([diamond]) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of halothane (Figure 1). Values represent means of triplicate measurements of two to four experiments for each enzyme.
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Figure 5. Comparison of isoflurane effects on ATPase activities in red blood cell membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 4.
Figure 5. Comparison of isoflurane effects on ATPase activities in red blood cell membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 4.
Figure 5. Comparison of isoflurane effects on ATPase activities in red blood cell membranes. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 4.
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Figure 6. Inhibition of ATPase activities in synaptosomal membranes by sodium pentobarbital. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of the barbiturate (Figure 1). Values represent means of triplicate measurements of 2-4 experiments for each enzyme.
Figure 6. Inhibition of ATPase activities in synaptosomal membranes by sodium pentobarbital. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of the barbiturate (Figure 1). Values represent means of triplicate measurements of 2-4 experiments for each enzyme.
Figure 6. Inhibition of ATPase activities in synaptosomal membranes by sodium pentobarbital. The PMCA (open circle), Sodium sup +, Potassium sup + -ATPase (closed square), and Magnesium2+ -ATPase (closed circle) activities were determined as described in materials and methods and the legend to Figure 1. One hundred percent is the activity of each adenosine triphosphatase in the absence of the barbiturate (Figure 1). Values represent means of triplicate measurements of 2-4 experiments for each enzyme.
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Table 1. Comparison of Clinical (EC50) and Inhibitory (I50) Potencies of Anesthetics
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Table 1. Comparison of Clinical (EC50) and Inhibitory (I50) Potencies of Anesthetics
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