An investigation into the role of hydroxyl radical in xanthine oxidase-dependent lipid peroxidation

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS Vol. 216, No. 1, June, pp. 142-151, 1982

An Investigation into the Role of Hydroxyl Radical in Xanthine Oxidase-Dependent Lipid Peroxidation MING Lkpartment

TIEN,

BRUCE

of Biochemistry,

A. SVINGEN, Michigan

AND STEVEN

D. AUST’

State University, East Lansing, Michigan

.68824

Received October 14,1981, and in revised form February 6,1982

A model lipid peroxidation system dependent upon the hydroxyl radical, generated by Fenton’s reagent, was compared to another model system dependent upon the enzymatic generation of superoxide by xanthine oxidase. Peroxidation was studied in detergent-dispersed linoleic acid and in phospholipid liposomes. Hydroxyl radical generation by Fenton’s reagent (FeClz + HzOz) in the presence of phospholipid liposomes resulted in lipid peroxidation as evidenced by malondialdehyde and lipid hydroperoxide formation. Catalase, mannitol, and Tris-Cl were capable of inhibiting activity. The addition of EDTA resulted in complete inhibition of activity when the concentration of EDTA exceeded the concentration of Fe 2+. The addition of ADP resulted in slight inhibition of activity, however, the activity was less sensitive to inhibition by mannitol. At an ADP to Fe2+ molar ratio of 10 to 1, 10 m&i mannitol caused 25% inhibition of activity. Lipid peroxidation dependent on the enzymatic generation of superoxide by xanthine oxidase was studied in liposomes and in detergent-dispersed linoleate. No activity was observed in the absence of added iron. Activity and the apparent mechanism of initiation was dependent upon iron chelation. The addition of EDTA-chelated iron to the detergent-dispersed linoleate system resulted in lipid peroxidation as evidenced by diene conjugation. This activity was inhibited by catalase and hydroxyl radical trapping agents. In contrast, no activity was observed with phospholipid liposomes when iron was chelated with EDTA. The peroxidation of liposomes required ADP-chelated iron and activity was stimulated upon the addition of EDTA-chelated iron. The peroxidation of detergent-dispersed linoleate was also enhanced by ADPchelated iron. Again, this peroxidation in the presence of ADP-chelated iron was not sensitive to catalase or hydroxyl radical trapping agents. It is proposed that initiation of superoxide-dependent lipid peroxidation in the presence of EDTA-chelated iron occurs via the hydroxyl radical. However, in the presence of ADP-chelated iron, the participation of the free hydroxyl radical is minimal.

The one-electron reduction of molecular oxygen to superoxide (0;) has been demonstrated to occur during many biochemical reactions, including the autoxidation of reduced flavins (1) and ferridoxins (2) and in certain enzymatic reactions (3, 4). Superoxide dismutase (SOD)2 rapidly dis-

mutates 0; to H202 and ground-state oxygen (Reaction [l]) (5). Hydrogen peroxide is in turn metabolized by catalase and glutathione peroxidase (6,7). The deleterious effects of 0~ and H202 may arise in cases where the production of these forms of oxygen exceeds their rates of metabolism. This may occur under conditions of excess oxygen (8) or upon exposure to xenobiotics

r To whom correspondence should be addressed. ’ Abbreviations used: SOD, superoxide dismutase; BHT, butylated hydroxytoluene; MDA, malondialdehyde; LOOH, lipid hydroperoxides; DMPO, 5,5-di9003-9361/82/070142-10$62.00/0 Copyright All rights

Q 1982 by Academic Press, Inc. of reproduction in any form reserved.

methyl-1-pyrrolline-N-oxide; liquid chromatography. 142

HPLC, high-pressure

HYDROXYL

RADICAL-DEPENDENT

which undergo cyclic reduction and autoxidation, such as paraquat (9), 6-hydroxydopamine (lo), or adriamycin (11, 12). Lipid peroxidation has been suggested to result from excess 0; production (9-12). However, the reactive form(s) of oxygen involved in OH-dependent lipid peroxidation has not been unequivocally established. Superoxide has been demonstrated not to be exceptionally reactive with a large number of organic substrates, including polyunsaturated fatty acids (13, 14). The reduction of transition metals such as iron by 05 has been demonstrated (15) and the reaction of ferrous iron with HzOz, produced by 0s dismutation, is known to produce the very reactive hydroxyl radical (. OH) (16). The sequence of reactions described (Reactions [2], [3]) is called the iron-catalyzed Haber-Weiss reaction: 2H+ + 205 - HzOz + 02,

PI

0; + Fe3+ - Fe’+ + O2 ,

PI

Fe’+ + HzOz -

Fe3+ + OH- + . OH.

[3]

Thus, the O;-dependent production of +OH and its involvement in lipid peroxidation has been proposed by several investigators both in the case of xanthine oxidase-promoted lipid peroxidation (14, 17-19) and for microsomal NADPH-dependent lipid peroxidation (14, 20, 21). In this report Fe’+ and H202, termed the Fenton’s reagent (Reaction [3]) has been utilized to initiate lipid peroxidation. The response of this . OH-dependent lipid peroxidation system to the presence of iron chelation agents, and to known inhibitors of . OH-dependent reactions has been characterized and compared to the results of similar studies utilizing a lipid peroxidation system dependent upon the superoxide anion. MATERIALS

AND METHODS

Materials, Cyctochrome c (Type VI), 2-thiobarbituric acid, NADPH, ADP, BHT, mannitol, Lubrol, and sodium benzoate were purchased from Sigma Chemical Company. Linoleic acid was obtained from Nu Chek Prep, Elysian, Minnesota. All other chemicals used were of analytical grade. All buffers and

LIPID PEROXIDATION

143

reagents were passed through Chelex 100 (Bio-Rad Laboratories) ion-exchange resin to free them of contaminants. Enqmes. Bovine erythrocyte SOD (2969 unita/mg protein), beef liver catalase (30,996 unita/mg protein), and xanthine oxidase (0.9 unit/mg protein) were obtained from Sigma Chemical Company. Gel filtration chromatography on Sephadex G-25 was used to remove the antioxidant thymol from catalase and the ammonium sulfate from xanthine oxidase. After chromatography, xanthine oxidase activity was measured by aerobic reduction of cytochrome c (22) and a unit of activity is defined as 1 pmol cytochrome c reduced/min. SOD activity was measured by the method of McCord and Fridovich (22). Catalase activity was measured by the procedure of Holmes and Masters (23) and a unit of activity is defined as 1 rmol HzOz decomposed/min. hficrosomal lipid. Male Sprague-Dawley rats (250274 g) were obtained from Spartan Research Animals (Haslett, Mich.). Liver microsomes were isolated by the method of Pederson et al. (24). Microsomal lipid was extracted from freshly isolated microsomes by the method of Folch et aE. (25). All solvents used for extractions were purged with argon and all steps were performed at 4°C to minimize autoxidation of unsaturated lipids. Extracted lipid was stored in argon-saturated CHCls:CHzOH (2:l) at -20°C. Lipid phosphate determinations were performed by the method of Bartlett (26). Reaction mixtures. Liposomes were prepared by sonication of the extracted microsomal lipid in argon-saturated distilled deionized water at 4°C (24). Liposomal peroxidation reactions initiated by the Fenton’s reagent were accomplished by the addition of FeCle to incubations containing HzOc and liposomes (1 pmol lipid phosphate/ml) in 36 mM NaCl, pH 7.5. The concentrations of FeClz and HeOz are as specified in the figures and tables. Other additions or deletions are as specified in the legends to the figures and tables. These reactions were initiated by the addition of FeClz. Xanthine oxidase-dependent peroxidation of liposomes was performed by incubating liposomes (1 pmol lipid phosphate/ml) with xanthine oxidase (0.1 unit/ml), EDTA-Fe’+ (0.11 mM EDTA, 0.1 mM FeCL), ADP-Fe’+ (1.7 mM ADP, 0.1 mM FeC13) and 0.33 mM xanthine in 30 mM NaC1, pH 7.5. Reactions were initiated by the addition of xanthine oxidase. Other additions or deletions are as specified in the table and figure legends. Incubations were done in a metabolic shaking water bath at 37°C under an air atmosphere. Although the reaction mixtures were unbuffered, the pH did not change during the course of the reactions. At 0, 3, and 6 min, xanthine oxidase-dependent lipid peroxidation reaction mixtures were sampled for MDA and LOOH content (27). The rates of peroxidations were linear within this time span. The MDA content was determined by

144

TIEN, SVINGEN, AND AUST

the thiobarituric acid test (27). To prevent further peroxidation of lipid during the assay procedure for MDA, 0.03 vol of 2% BHT in ethanol was added to the thiobarbituric acid reagent (27). The LOOH content was determined iodometrically (27). Linoleate stock solutions were made by suspending linoleic acid (100 mg) into argon-purged Chelexed water by adding 5-10 drops of 6 N NaOH to yield a clear solution. The pH of this solution was then slowly lowered to 7.5 by the addition of 6 N HCl. The resultant micelle solution was taken up to a final volume of 50 ml and used immediately. Lipid peroxidation of detergent-dispersed linoleate was accomplished by incubating sodium linoleate (5.7 mM) with xanthine oxidase (6.6 munit/ml), Lubrol (l%), 35 rnM acetaldehyde, EDTA-Fe’+ (0.11 mM EDTA, 0.1 mM FeClv), and ADP-Fe*+ (0.5 mM ADP, 0.1 mM FeC&) in 30 mu NaCl, pH 7.5, at 3’7’C, under air. Other additions or deletions are as indicated in the table legends. Reactions were initiated by the addition of xanthine oxidase. These incubations were carried out in a cuvette in a Cary 219 spectrophotometer. Diene conjugation during lipid peroxidation was continuously monitored by the absorbance change at 234 nm (23). The rate of diene conjugation was linear for up to approximately 5 min, after which a decrease in rate was observed. All rates were determined from the initial velocity of the reaction. The data shown are results of representative experiments. Otti methods ADP-chelated and EDTA-chelated iron solutions were prepared by the addition of either FeCla or FeCla to chelate solutions adjusted to pH 7.5. Due to the pH change from the addition of FeC&, the pH of these chelate solutions was readjusted to

6

t

FIG. 2. Effect of hydrogen peroxide concentration on hydroxyl radical-dependent lipid peroxidation. Reaction mixtures contained liposomes (1 pmol lipid phosphate/ml), 0.2 mM FeC&, and the specified amount of HeOr in 30 mM NaCl, pH 7.5, at 37°C. Incubation and assay conditions are described under Materials and Methods.

7.5. No changes in pH were observed from the addition of FeCla to the chelate solutions. Water used in the preparation of the ferrous solutions was argon purged to minimize Fee+ autoxidation. Since most buffers are iron chelators or reactive with hydroxyl radical, the reaction mixtures were not buffered. Consequently, the pH of all reagents was carefully adjusted to 7.5 prior to use. RESULTS

Hgdmxyl

Radicul-Dependent

The reaction of H202 with Fe2+ (Fenton’s reagent) has been demonstrated to produce the . OH (15). The formation of this radical has been demonstrated with EPR spin-trapping techniques utilizing DMPO (29). The EPR spectrum has a 1:2:2:1 signal intensity pattern, a g value of 2.006 and hyperfme splitting constants of AN = 14.95 G and AH = 14.95 G. To confirm the formation of the OH in our system, this spectrum was reproduced by the reaction of 0.15 mM Fe2+ and 0.1 InM H202 in the presence of 60 mM DMPO (not shown). The generation of the . OH in the presence of liposomes resulted in lipid peroxidation as evidenced by a rapid rate of LOOH and MDA formation (Fig. 1). The rate of MDA l

FIG. 1. Time course of hydroxyl radical-dependent lipid peroxidation. Reaction mixtures contained liposomes (1 pmol lipid phosphate/ml), 0.1 rnre HaOa, and 0.2 rnlld FeCla in 30 ml NaCl. pH 7.5, at 37°C. Incubation and assay conditions are described under Materials and Methods.

tipid

HYDROXYL

RADICAL-DEPENDENT

[FeCI~hM) FIG. 3. Effect of FeCle concentration on hydroxyl radical-dependent lipid peroxidation. Reaction mixtures contained liposomes (1 pmol lipid phosphate/ ml), 0.1 mb%HsO, and the specific amount of FeCle in 30 mM NaCI, pH 7.5, at 37°C. Incubation and assay conditions are described under Materials and Methods.

formation was constant at 6.24 nmol/min/ ml up to 2 min after initiation of the reaction with Fe2’. The LOOH content, determined iodometrically (27) increased at a much greater rate (approximately 150 nmol/min/ml), but the rate of LOOH formation decreased after the first minute of the reaction. No detectable MDA or LOOH formation resulted from the separate addition of FeC12 or H202 to liposomes. The effect of H202 concentration on the rate of lipid peroxidation is illustrated in Fig. 2. At 0.2 mM FeC12, the rate of MDA formation reached a maximum when H202 concentration was about 0.1 mM. Concentrations of Hz02 greater than 0.1 mM caused a decrease in the rate of lipid peroxidation. At a constant H202 concentration of 0.1 mM, increasing FeC12 concentrations to about 0.1 mM resulted in a linear increase in the rate of MDA formation (Fig. 3). Higher concentrations of FeC12 had no effect on the rate of lipid peroxidation. Inhibition by mannitol or benzoate has been used as a criterion to assess . OH involvement in reaction mechanisms (14,1719). As shown in Table I, peroxidation of liposomes by Fenton’s reagent could be effectively inihibited by these aOH traps.

145

LIPID PEROXIDATION

At 10 InM, mannitol inhibited activity by 95% while 10 mM benzoate caused 88% inhibition. Tris-Cl is also an effective . OH trap (30) and 10 mbi Tris-Cl caused 92% inhibition of activity. Addition of 1 unit/ml catalase inhibited activity 93% (Table I) while boiled catalase had no effect. Most model lipid peroxidation systems employ iron chelates. In addition, biological systems are abundant in substances which can chelate iron. For these reasons, the effect of iron chelation on *OH-dependent lipid peroxidation was examined. ADP and EDTA were examined because both have been implicated in Fenton-type reactions to yield the . OH (14,16,31). The chelation of Fe2’ by EDTA in Fenton’s reagent resulted in inhibition of MDA formation (Fig. 4). Complete inhibition occurred when the ratio of EDTA to Fe2$ was equimolar. The chelation of Fe’+ by ADP resulted in slight inhibition of activity (Fig. 5). Activity in the absence of ADP could be completely inhibited by mannitol but as the concentration of ADP increased, the amount of activity inhibited by mannitol decreased, reaching 25% inhibition at an ADP to Fe’+ molar ratio of 10 to 1. TABLE HYDROXYL

I

RADICAL DEPENDENT PEROXIDATION PHOSPHOLIPID LIPOKIMES

Addition

MDA (nmol/min/mI)

None

0.01

Fe2+

0.15 0.10

Hz02

Fez+

OF

H 20 2

Fe2+’ H202, Fe’+: Hz02 Fe2+, H20d Fe*+, HrOs,

benzoate mannitol Tris-Cl catalase

3.45 0.41 0.22 0.29 0.25

Note. Liposomes (1 pmol lipid phosphate/ml) were incubated in 30 mild NaCl, pH 7.5, at 37°C. The following additions were made as indicated: 0.2 rnlu FeC12, 0.1 mM HrO, 1 unit catalase/ml, and 10 rnhf benzoate,mannitol, or Tris-Cl. Incubation and assay conditions are described under Materials and Methods.

146

TIEN, SVINGEN,

AND AUST

Xanthine Oxiclase-Dependent Pw~tim of Lipom?nes The requirements for xanthine oxidasedependent peroxidation of liposomes are shown in Table II. In the absence of iron, the generation of Op and HzO, by the action of xanthine oxidase on xanthine did not result in lipid peroxidation as assayed by LOOH and MDA formation. The addition of chelated iron to this reaction mixture caused a linear increase in both MDA and LOOH content. However, this increase was exceedingly sensitive to the iron chelators. Relatively low rates of lipid peroxidation were obtained by the addition of Fe3+ chelated by EDTA (Table II). The inclusion of Fe3+ chelated by ADP resulted in low levels of MDA and LOOH formation. Much greater rates of lipid peroxidation (2.02 nmol MDA/min/ml and 15.3 nmol LOOH/min/ml) occurred when both ADP-Fe3+ and EDTA-Fe3+ were included in the reaction mixture. The effect of unchelated Fe3+ on xanthine oxidasedependent peroxidation of liposomes was also examined, however, no activity was observed. The involvement of the . OH in xanthine

0

0

0.2

0.4

EDTA/Fe*

06

mob

0.8

lo

12

ratio

FIG. 4. Inhibition of hydroxyl radical-dependent lipid per-oxidation by EDTA. Reaction mixtures contained liposomes (1 pmol lipid phosphate/ml) and 0.1 maa HaOx in 30 mM NaCl, pH 7.5, at 3’7°C. EDTA concentration is expressed as molar ratios to FeCla. The FeClz concentrations were either 0.05 mbi (open circles) or 0.1 mM (closed circles). Incubation and assay conditions are described under Materials and Methods.

ADPI&

mdor

mtio

FIG. 5. Effect of ADP on hydroxyl radical-dependent lipid peroxidation. Reaction mixtures contained liposomes (1 pmol lipid phosphate/ml), 0.1 mM H,Or, 0.2 mbd FeCla, and the specified amount of ADP in 30 mM NaCl, pH 7.5, at 3’7°C. ADP concentration is expressed as molar ratios of FeClr. Incubations were performed in the presence (open circles) and absence (closed circles) of 10 mM mannitol. The precentage inhibition by mannitol as a function of ADP is plotted as open triangles. Incubation and assay conditions are described under Materials and Methods.

oxidase-dependent peroxidation of liposomes was investigated by the criteria utilized in investigating peroxidation of liposomes initiated by the Fenton’s reagent. Mannitol (10 mM) and Tris-Cl (50 mM), both very effective inhibitors of lipid peroxidation initiated by the Fenton’s reagent, were without effect in lipid peroxidation promoted by xanthine oxidase (Table III). SOD (1 unit/ml) was an effective inhibitor of lipid peroxidation, presumably by blocking the reduction of iron by 0;. However, catalase (1 unit/ml) did not inhibit the rate of lipid peroxidation, suggesting that the involvement of Hz02 in xanthine oxidase-dependent lipid peroxidation is minimal. The direct addition of HzOz caused a sharp decrease in the rates of MDA and LOOH formation (Fig. 6). Xanthine oxidase activity, as measured by uric acid formation, was also decreased by HzOz, however, this decrease was minimal and did not correlate with the decrease in the rate of lipid peroxidation. Hydrogen peroxide had no effect on the assays for MDA or LOOH (not shown).

HYDROXYL

TABLE

RADICAL-DEPENDENT

II

EFFECT OF IRON CHELATES ON XANTHINE OXIDASE-DEPENDENT PEROXIDATION OF PHOSPHOLIPID LIPOSOMES nmol/min/ml Addition

MDA

LOOH

None ADP-Fe=‘, EDTA-Fe’+ Xanthine oxidase Xanthine oxidase, ADP-Fe8+ Xanthine oxidase, EDTA-Fe’+ Xanthine oxidase, ADP-Fe’+, EDTA-Fe*+

0.02 0.02 0.02 0.29 0.18 2.02

0.1 0.4 0.6 2.2 1.0 15.3

Note. Reaction mixtures contained lipnsomes (1 rmol lipid phosphate/ml) and 0.33 mM xanthine in 30 mM NaCl, pH 7.5, at 3’7°C. The following additions were made as indicated: ADP-Fe*+, (1.7 mM ADP, 0.1 my Fe&), EDTA-Fea+ (0.11 mbi EDTA, 0.1 mndFeCl& and 0.1 unit xanthine oxidase/ml. Incubation and assay conditions are described under Materials and Methods.

Xanthine O&&se-Dependent Peroxidation of Detergent-Dispersed Linokate In a recent report, Fridovich and Porter (19) demonstrated that EDTA-Fe3+ facilitated the xanthine oxidase-dependent peroxidation of detergent-dispersed arachidonate. Our results with liposomes indicated that EDTA-Fe3+ was not effective in catalyzing xanthine oxidase-dependent lipid peroxidation. For these reasons, xanthine oxidase-dependent lipid peroxidation was also studied using detergent-dispersed linoleate as the substrate. The extent of lipid peroxidation was monitored by the increase in absorbance at 234 nm due to conjugated diene formation. The formation of conjugated diene hydroperoxides, and the corresponding increase in absorbance at 234 nm was verified by HPLC analysis of the products. The extracted products of xanthine oxidase-dependent peroxidation of linoleate were shown to have similar retention times as linoleate hydroperoxides generated by soybean lipoxidase (not shown). Due to the intense ultraviolet absorbance of xanthine and ADP, modification of the experimental conditions was necessary to monitor diene conjugation. Acetaldehyde was uti-

LIPID

147

PEROXIDATION

lized as the substrate for xanthine oxidase and the ADP concentration of ADP-Fe3+ solutions was lowered from 1.7 to 0.5 mM. Further studies with xanthine oxidase-dependent peroxidation of liposomes demonstrated that this change in ADP concentration did not affect the rate of peroxidation (not shown). Table IV shows the effect of different iron chelates on the peroxidation of detergent-dispersed linoleate. Again, no activity was observed in the absence of added iron. In contrast, to the results with liposomes, the addition of EDTA-Fe3+ resulted in a linear increase in diene conjugation of dispersed linoleate (AAW = O.O70/min/ml). The rate of diene conjugation was slightly higher in the presence of ADP-Fe3+ (ti= = O.O85/min/ml) while the addition of both iron complexes resulted in maximal rates of lipid peroxidation (AAW = O.O92/min/ml). The effects of SOD, catalase, and various . OH trapping agents on xanthine oxidase-dependent lipid peroxidation were studied in the presence of EDTA-Fe3+, ADP-Fe3+, or EDTA-Fe3+ plus ADP-Fe3+. The results are summarized in Table V. It is clear that

TABLE

III

EFFECT OF VARIOUS SCAVENGERS ON XANTHINE OXIDASE-DEPENDENT PEROXIDATION OF PHOSPHOLIPID LIPOSOMES nmol/min/ml Addition

MDA

LOOH

None

2.02 2.23 0.03 2.32 2.25

15.3 17.3 5.0 14.5

Catalase SOD

Mannitol Tris-Cl

17.1

Note. The complete system contained liposomes (1 pmol lipid phosphate/ml), ADP-Fe*+ (1.7 mM ADP, 0.1 mM FeCls), EDTA-Fe3’ (0.11 mM EDTA, 0.1 mM FeC&), 0.33 mM xanthine, and 0.1 unit xanthine ox-

idase/ml in 30 mM NaCI,

pH 7.5, at 37’C. The following additions were made as indicated: 1 unit catalaselml, 1 unit SOD/ml, 10 rnn! mannitol, and 50 mM Tris-Cl. Incubation and assayed conditions are described under Materials and Methods.

143

TIEN. SVINGEN. AND AUST

SOD (10 units/ml) was a potent inhibitor of lipid peroxidation in all three systems. Essentially no inhibition was observed with catalase (1,5 and 10 units/ml), mannitol (10 and 50 mM), or ethanol (10 and 50 DIM) on lipid peroxidation in the presence of ADP-Fe3+ while significant inhibition occurred in the presence of EDTAFe3+. These agents caused only modest inhibition of lipid peroxidation in the presence of both iron complexes. DISCUSSION

The results of these experiments demonstrate that peroxidation of liposomes can be initiated by . OH generated by Fenton’s reagent. EPR spin-trapping experiments with DMPO confirmed the formation of - OH by Fe2+ and H,Oz. The addition of mannitol or benzoate effectively inhibited lipid peroxidation of liposomes initiated by Fenton’s reagent. The involvement of H202 was illustrated by inhibition of lipid peroxidation by catalase. The rate of lipid peroxidation was highly sensitive to both FeCl, and H20z concentrations. High concentrations of H202 caused a slight inhibition of lipid peroxidation. This may be due to the dual role of H202 as a substrate

I

1

TABLE

EFFECT OF IRON CHELATES ON XANTHINE OXIRASEDEPENDENT PEROXIDATION OF DETRRGENTDISPERSED LINOLEATE Addition None ADP-Fe?+ EDTA-Fe”+ ADP-Fe”+, Xanthine Xanthine Xanthine Xanthine

[H&d

0.5

0.6

0.7

0.6 0.9

(m)

FIG. 6. Inhibition of xanthine oxidase-dependent lipid peroxidation by HzOe. Reaction mixtures contained liposomes (1 rmol lipid phosphate/ml), ADPFeS+ (1.7 mM ADP, 0.1 mbf FeC18), EDTA-Fe’+ (0.11 mM EDTA, 0.1 mM FeCl& 0.33 m&f xanthine, 0.1 unit xanthine oxidase/ml, and the specified amount of HeOz in 30 mM NaCl, pH 7.5, at 3’7’C. Incubation and assay conditions are described under Materials and Methods.

M&min/ml

EDTA-Fe”+ oxidaae oxidaae, ADP-Fe* oxidase, EDTA-Fee+ oxidaae, ADP-Fe”, EDTA-FL?+

<0.001
Note. Reaction mixtures contained 5.7 mM sodium linoieate, 1% Lubroi, and 35 mM acetaldehyde in 30 rnlu NaCl, pH 7.5. The following additions were made ae indicated: ADP-Fee+ (0.5 mM ADP, 0.1 rnM FeCI.&, EDTA-Fee+ (0.11 rnM EDTA, 0.1 mM Fe&), and xanthine oxidaae (6.6 X lo-‘unit/ ml). Diene conjugation was assessed by continuous monitor of increase in 234-nm absorbance. Incubation and assay conditions are described under Materials and Methods.

for . OH formation and also as a . OH trap. The rate of constant for . OH reacting with H202 is 4.5 X 10” M-’ s-l (32): - OH + Hz02 --) Hz0 + 0; + H+.

[4]

Thus, at high concentrations, H202 may be competing with polyunsaturated lipid for the *OH resulting in decreased rates of lipid peroxidation. Ferrous ion has also been demonstrated to be highly reactive with . OH, resulting in a termination reaction (32). Although this reaction, Fe2+ + * OH -

0.1 0.2 0.3 0.4

IV

Fe3+ + OH-,

r51

proceeds with a second-order rate constant of 3 X 10’ M-’ s-’ (32), high Fe2+ concentrations did not inhibit lipid peroxidation under the experimental conditions employed. The participation of Fe” in secondary initiation reactions with LOOH, thus augmenting the rates of lipid peroxidation (33), may account for the lack of inhibition observed at high FeC12 concentrations. The effect of iron chelation by EDTA or ADP on the Fenton’s reagent was examined since both these chelates have been used to study xanthine oxidase-dependent lipid peroxidation (14,19, 31). EDTA chelation of Fe3+ has been reported to facil-

HYDROXYL

RADICAL-DEPENDENT TABLE

LIPID PEROXIDATION

149

V

EFFECT OF VARIOUS SCAVENGERS ON XANTHINE OXIDASE-DEPENDENT PEROXIDATION OF DETERGENT-DISPERSED LINOLEATE Percentage inhibition Addition None 10 units/ml SOD 1 unit/ml Catalase 5 units/ml Catalase 10 units/ml Catalase 10 m?d Mannitol 50 rnM Mannitol 10 mM Ethanol 40 mM Ethanol

EDTA-Fe3+ (0.070) 91 20 37 40 19 31 26 37

ADP-Fe3+ (0.085) 90 3 3 0 0 0 1 2

EDTA-Fe3+ , ADP-Fea+ (0.092) 8.3 0 3 4 8 9 4 9

Note. The effect of SOD, catalase, and various *OH trapping agents were studied on lipid peroxidation in the presence of EDTA-Fe ‘+ , ADP-Fe’+, or EDTA-Fee’ plus ADP-Fea+. The iron chelate concentrations were 0.11 mM EDTA, 0.1 mM FeC13, and 0.5 mM ADP, 0.1 m&f FeCls. All reaction mixtures contained 5.7 rnrd sodium linoleate, 1% Lubrol, 35 mM acetaldehyde, and 6.6 X 10v3 unit/ml xanthine oxidase in 30 mM NaCl, pH 7.5. Additions were made as indicated. Rates are expressed as the percentage inhibition. The value in parenthesis represent the initial velocities of the reaction expressed in PA,/min/ml. Diene conjugation was assessed by continuous monitor of increase in 234-nm absorbance. Incubation and assay conditions are described under Materials and Methods.

itate catalysis of the Haber-Weiss reaction (1534). Catalysis of the Haber-Weiss reaction involves initial reduction of Fe3+ by 05 followed by reduction of Hz02 by the reduced iron. Our results show that the latter reaction, the Fenton’s-type reaction, is inhibited by EDTA chelation of Fe2+. Further studies on the autoxidation of Fez+ (measured by oxygen consumption using a Clark electrode (indicated that EDTA chelation resulted in a rapid autoxidation of Fe’+. Thus the inhibition of * OH-dependent lipid peroxidation observed by EDTA chelation of Fe*+ is most likely the result of a decrease concentration of Fe*+ due to autoxidation. The observed enhancement of the iron catalyzed Haber-Weiss reaction by EDTA (15, 34) is probably due to facilitation of the reduction of Fe3’ by 0;. The inclusion of ADP in the Fenton’s reagent caused a slight decrease in the rate of lipid peroxidation. This slight decrease could also be attributed to autoxidation of Fe2+ facilitated by ADP. Oxygen consumption experiments indicated that ADP chelation also enhanced the rate of

Fe’+ autoxidation, however, these rates were much slower than those observed with EDTA (not shown). Although purine nucleotides have been shown to react with the . OH (35), 10 mM ADP only caused a 10% decrease in activity. In addition, lipid peroxidation initiated by FeCl, and H20e in the presence of ADP was less sensitive to mannitol inhibition. These results suggest that ADP chelation of Fe’+ results in lipid peroxidation that is not dependent upon the . OH. However, it is possible that ADP reacts with the *OH to yield a radical product that does not react with mannitol but is capable of initiating lipid peroxidation. These possibilities are currently under investigation. In accord with the report of Lai and Piette (31), our results indicate that in the presence of EDTA-Fe3’, initiation of xanthine oxidase-dependent lipid peroxidation occurs via the *OH. In a homogeneous system of detergent-dispersed linoleate, the EDTA-Fe’+-dependent generation of the . OH resulted in lipid peroxidation as evidenced by diene conjugation. The inhibition of activity by SOD,

150

TIEN, SVINGEN,

catalase, mannitol, and ethanol suggests that initiation occurs via the iron-catalyzed Haber-Weiss reaction. However, in liposomes, the generation of 0; and H202 by the action of xanthine oxidase and xanthine in the presence of EDTA-Fe3+ did not result in lipid peroxidation. This difference in activity would suggest a correlation between proximity of . OH generation and its lipid peroxidation-initiating activity. In the case of liposomes, OH generation would probably occur in the aqueous phase. It is unlikely that the highly reactive *OH would diffuse away from the site of formation to liposomes to initiate lipid peroxidation (16). Dispersion of the lipid with detergent to yield a homogeneous phase would bring the lipid in closer proximity to the site of . OH formation, thus resulting in lipid peroxidation. In contrast to the results with EDTAFe3+, . OH participation in xanthine oxidase-dependent lipid peroxidation appears minimal in the presence of ADP-Fe3+. Catalase and *OH trapping agents, at concentrations which caused complete inhibiton of Fenton’s reagent-dependent peroxidation of liposomes, were without effect on xanthine oxidase-dependent peroxidation of liposomes in the presence of ADP-Fe3+. However, SOD was an effective inhibitor of xanthine oxidase-dependent peroxidation of liposomes causing a 97% decrease in the rate of MDA formation and a 67% decrease in the rate of LOOH formation. The addition of H202 to xanthine oxidase-dependent peroxidation of liposomes actually resulted in decreased rates of peroxidation. In the detergentdispersed linoleate system, the concentrations of catalase and . OH trapping agents which caused significant inhibition of EDTA-Fe3+-dependent peroxidation were not effective in the presence of ADPFe3+. In liposomes and detergent-dispersed linoleate, the addition of both EDTA-Fe3+ and ADP-Fe3+ resulted in the maximal rate of lipid peroxidation. Again, catalase and -OH trapping agents were without effect. In could be argued that ADP-Fe3+ localizes the generation of the . OH closer to the lipid such that waterl

AND ATJST

soluble trapping agents cannot effectively scavenge the *OH. This would suggest an affinity of ADP for the lipid phase. However, preliminary experiments where liposomes and ADP-Fe3+ were incubated prior to filtration to separate the liposomes from the aqueous phase showed no evidence for enrichment of iron in the lipid phase as assayed by atomic plasma emission spectroscopy. Moreover, detergent dispersion of the lipid phase into a homogeneous system did not render ADPFe3+-dependent peroxidation more susceptable to catalase or . OH trapping agents. Our results on xanthine oxidase-dependent lipid peroxidation in the presence of ADP-Fe3+ are in agreement with the results of Svingen et al. (36) and Tyler (13). Svingen and co-workers proposed that initiation of lipid peroxidation occurred via an ADP-iron-oxygen complex. Although we have no direct evidence for such a complex, our results support this possibility. In addition, these workers proposed that enhancement of lipid peroxidation by EDTA-Fe3+ is a result of EDTA-Fe3+ (upon reduction to EDTA-Fe2+ by OH)-catalyzed decomposition of LOOH resulting in accelerated peroxidation through lipid hydroperoxide-dependent initiation reactions. Although our results and the results of others (19, 31) suggest that the role of EDTA-Fe’+ in xanthine oxidase-dependent lipid peroxidation is catalysis of the Haber-Weiss reaction, it is probable that once lipid hydroperoxides are formed, EDTA-Fe2+ acts to reductively cleave these lipid hydroperoxides as it can with H202. This may account for the high rates of lipid peroxidation observed in the presence of both EDTA-Fe’+ and ADP-Fe3+. Fong and co-workers (14) also studied xanthine oxidase-dependent lipid peroxidation in the presence of ADP-Fe3+. These workers reported that SOD stimulated while catalase and . OH trapping agent inhibited O;-induced lysis of lysosomes. Aside from different methods used for assessing lipid peroxidation, we have no apparent explanation for the discrepancy in results. Our results with a model system of ADP-Fe3+ and liposomes, which we

HYDROXYL

RADICAL-DEPENDENT

would anticipate to have more biological significance than EDTA-Fe3+ with detergent-dispersed linoleate, indicate that 05 -dependent lipid peroxidation proceeds through a mechanism not dependent upon the *OH. Although the exact nature of this initiating complex remains unknown, thermodynamic considerations require that this initiation complex be of oxidizing strength equivalent to that of the . OH. However, it is apparent that the generation of free . OH is not required for its lipid peroxidation-initiating activity. ACKNOWLEDGMENTS We would like to thank Dr. John Bucher for assistance in preparation of this manuscript. The teehnical assistance of John Vitkuske is greatly appreciated. We would also like to acknowledge the secretarial assistance of Cathy M. Custer. Supported by NSF Grant PCM 79-15328, Michigan Agricultral Experiment Station Journal Article 10019.

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