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OtherPROSTAGLANDINS, LEUKOTRIENES AND OTHER EICOSANOIDS

Cytochrome P450-Derived Arachidonic Acid Metabolism in the Rat Kidney: Characterization of Selective Inhibitors

Mong-Heng Wang, Elimor Brand-Schieber, Barbara A. Zand, Xuandai Nguyen, John R. Falck, Narayanan Balu and Michal Laniado Schwartzman
Journal of Pharmacology and Experimental Therapeutics March 1998, 284 (3) 966-973;

Abstract

We characterized the inhibitory activity of several acetylenic and olefinic compounds on cytochrome P450 (CYP)-derived arachidonic acid ω-hydroxylation and epoxidation using rat renal cortical microsomes and recombinant CYP proteins. Among the acetylenic compounds, 6-(2-propargyloxyphenyl)hexanoic acid (PPOH) and N-methylsulfonyl-6-(2-propargyloxyphenyl)hexanamide were found to be potent and selective inhibitors of microsomal epoxidation with IC50 values of 9 and 13 μM, respectively. On the other hand, 17-octadecynoic acid inhibited both ω-hydroxylation and epoxidation of arachidonic acid with IC50 values of 7 and 5 μM, respectively. The olefinic compounds N-methylsulfonyl-12,12-dibromododec-11-enamide (DDMS) and 12,12-dibromododec-11-enoic acid (DBDD) exhibited a high degree of selectivity inhibiting microsomal ω-hydroxylation with an IC50 value of 2 μM, whereas the IC50 values for epoxidation were 60 and 51 μM for DDMS and DBDD, respectively. Studies using recombinant rat CYP4A isoforms showed that PPOH caused a concentration-dependent inhibition of ω-hydroxylation and 11,12-epoxidation by CYP4A3 or CYP4A2 but had no effect on CYP4A1-catalyzed ω-hydroxylase activity. On the other hand, DDMS inhibited both CYP4A1- and CYP4A3- or CYP4A2-catalyzed arachidonic acid oxidations. Inhibition of microsomal activity by PPOH, but not DDMS, was time- and NADPH-dependent, a result characteristic of a mechanism-based irreversible inhibitor. These studies provide information useful for evaluating the role of the CYP-derived arachidonic acid metabolites in the regulation of renal function and blood pressure.

The CYP monooxygenases constitute a major metabolic pathway for arachidonic acid in the rat kidney. The CYP proteins are primarily localized to the cortex with high concentrations in the proximal tubules, vasculature and thick ascending limb of Henle’s loop (TALH), where they metabolize arachidonic acid mainly to 20-HETE as well as to 19-HETE and EETs (Hardwick, 1991; Omata et al., 1992; Dees et al.,1982; Ma et al., 1993). Hydroxylation of arachidonic acid at the ω-carbon to form 20-HETE is primarily catalyzed by isoforms of the CYP4A family (Kimura et al., 1989a; Kimura et al., 1989b; Stromstedt et al., 1990; Laniado Schwartzman et al., 1996). On the other hand, arachidonic acid epoxidation is much less specific and can be carried out by numerous CYP isoforms from different CYP gene families, including 1A1, 1A2, 2B1, 2B4, 2C2, 2C9, 2C11, 2C23, 2E1 and 2G1 (Laethem et al., 1994; Laethem and Koop, 1992; Laethem et al.,1993; Rifkind et al., 1995). In addition to having a broad spectrum of substrate specificity, CYP isoforms also demonstrate a lack of product specificity; i.e., one protein can catalyze the oxidation of arachidonic acid at multiple sites. For example, we have shown that CYP4A2 functions not only as an arachidonate ω-hydroxylase but also as an arachidonate 11,12-epoxygenase (Wang et al.,1996).

The potential role of the CYP-derived arachidonic acid metabolites in the regulation of renal function and in hypertension has been documented in numerous studies. 20-HETE, in vitro, is a potent vasoconstrictor of renal arterioles (Ma et al., 1993;Imig et al., 1996; Zou et al., 1996c) and an inhibitor of renal tubular transport and K+ channel activity (Escalante et al., 1994; Wang and Lu, 1995).In vivo, 20-HETE affects renal vascular resistance, autoregulation of renal blood flow and tubuloglomerular feedback (Gebremedhin et al., 1993; Kauser et al., 1991;Zou et al., 1994a; Zou et al., 1996a; Zouet al., 1994b). In the kidney, EETs exhibit a broad and contrasting spectrum of biological activities, including vasodilation and vasoconstriction (Carroll et al., 1992; Zou et al., 1996b; Katoh et al., 1991) as well as inhibition and stimulation of ion transport mechanisms (Harris et al.,1990; Takahashi et al., 1990; Sakairi et al.,1995; Hirt et al., 1989). Studies using different animal models of hypertension and CYP inhibitors have implicated both epoxidation and hydroxylation products of arachidonic acid in the renal responses to changes in dietary salt levels and in hypertension (Sacerdoti et al., 1989; Makita et al., 1994;Imig et al., 1993; Zou et al., 1994c; Capdevilaet al., 1992; Brand-Schieber et al., 1996).

In order to elucidate the physiological and pathophysiological roles of these arachidonic acid metabolites, it is important to inhibit one CYP-catalyzed reaction selectively without affecting the others. The fact that the CYP monooxygenases exist in many isoforms with relatively high homology and broad substrate specificity complicates this task; enzyme inhibitors are frequently nonspecific, and multiple isoforms often demonstrate similar catalytic activities (Gonzalez, 1988). A relatively new approach to inhibiting CYP activities selectively involves the use of “suicide substrates” that were designed to resemble the substrate and at the same time to inactivate the enzyme. Inactivation is irreversible, and activity is restored on de novo synthesis of the enzyme. Acetylenic derivatives, such as 17-ODYA, have been designed to be selective inhibitors of CYP-derived fatty acid ω-hydroxylation (Muerhoff et al., 1989). The effect of 17-ODYA on renal function has been studied extensively by Zouet al. (1994c), who reported that infusion of 17-ODYA into either renal artery or cortical interstitium increased papillary blood flow, urine flow and sodium excretion without affecting glomerular filtration rate and cortical blood flow. However, because 17-ODYA inhibited ω-hydroxylation and epoxidation of arachidonic acid with similar potency (Zou et al., 1994c), it is difficult to sort out the relative contribution of these metabolites to the overall effect of the drug. Therefore, there is a need for selective inhibitors that will expedite the determination of the role of each pathway in the regulation of renal function and hypertension.

In the present study, we characterize the effect of several acetylenic and olefinic fatty acid analogs on ω-hydroxylation and epoxidation of arachidonic acid in rat renal cortical microsomes and on recombinant rat CYP4A isoforms. This study provides information useful for evaluating the role of the CYP-arachidonic acid metabolites in the regulation of renal function and blood pressure.

Materials and Methods

Materials.

The following drugs and chemicals were used in this study: [1-14C]-arachidonic acid (56 mCi/mmol) (DuPont-New England Nuclear, Boston, MA), purified recombinant rat NADPH-CYP (c) oxidoreductase (OR) (specific activity, 58 μmol/min/mg) (Oxford Biomedical Research Inc., Oxford, MI), 17-ODYA (Cayman Chemical Co., Ann Arbor, MI), emulgen E911 (KAO Atlas, Tokyo, Japan), tissue culture and molecular biology reagents (Gibco-BRL, Gaithersburg, MD), Sf9 insect cells and the liposome DNA transfection kit (Invitrogen, San Diego, CA) and purified rat liver cytochrome b5 (specific activity, 40 nmol/mg) (Panvera Corp., Madison, WI). All solvents were HPLC grade.

Synthesis of CYP inhibitors.

The structures of all compounds are shown in figure 1. The compounds PPOH, MS-PPOH, DDMS, DBDD and DPMS were synthesized and their structures confirmed by spectral analysis as described by Falcket al., in press.

Figure 1
Figure 1

Chemical structures of CYP inhibitors.

Tissue and microsome preparations.

Male Sprague-Dawley rats (8 weeks old, Charles River, Wilmington, PA) were anesthetized with pentobarbital sodium (50 mg/kg i.p.). Kidneys were removed, and the cortex was dissected and homogenized in buffer containing 100 mM Tris-HCl and 1.15% KCl, pH 7.4. Homogenates were centrifuged at 10,000 × g for 30 min. Microsomes were obtained by centrifugation of the supernatant at 100,000 × g for 90 min and resuspended in 0.25 M sucrose buffer and stored at −80°C.

Preparation of recombinant CYP4A cell membranes.

CYP4A proteins were expressed in the baculovirus-Sf9 insect cell expression system as described previously (Wang et al., 1996). Briefly, CYP4A cDNAs were ligated into the Sma I site of the baculovirus expression vector, pVL1393. Transfection of the expression vector was performed individually by an AcMNPV linear transfection kit (Invitrogen). AcMNPV DNA (1 μg) was mixed with 3 μg of CYP4A-PVL1393 construct in a 5-ml polystyrene tube containing 1.5 ml of serum-free Grace medium. A mixture of 30 μg of cationic liposomes and 1.5 ml of serum-free medium was added to the DNA, mixed and added into cultured Sf9 cells dropwise. Transfected cells were incubated at 27°C overnight, after which the medium was removed, fresh medium was added, and the cells were incubated for 4 to 6 days. Identification of recombinant viruses was done by visualization of Occ-negative plaques, immunoblot and P450 spectral analysis. Recombinant viruses were amplified in Sf9 cells. The titer for recombinant viruses was determined by plaque assay. In order to prepare CYP4A recombinant cell membranes, Sf9 cells were infected with CYP4A recombinant viruses and cultured in the presence of hemin (4 μg/ml). After 72 h, the cells were harvested, washed with 0.14 M NaCl in 50 mM potassium phosphate (pH 7.2) and resuspended in sucrose buffer (50 mM potassium phosphate, pH 7.4, and 0.5 M sucrose). Cell lysates were prepared by brief sonication (4–5 bursts of 4-s duration) and subjected to high-speed centrifugation (100,000 × g) for 60 min. The membrane pellet was then resuspended in sucrose buffer and stored at −80°C. Protein concentration was measured according to the method of Bradford (BioRad; Melville, NY). CYP content was calculated from the reduced CO-difference spectrum using an extinction coefficient of 91 mM−1 (Omura and Sato, 1964).

Incubation conditions, metabolite extraction and HPLC separation.

Compounds (stock solution in ethanol) were diluted 10 to 20 fold with 100 mM potassium phosphate buffer, pH 7.5. The final concentration of ethanol in the incubations was 0.5% (v/v). At this concentration of ethanol, there was no effect on the activities of ω-hydroxylation and epoxidation of arachidonic acid. The diluted solution was then added into the incubation mixture consisting of microsomes (150 μg of protein), 1 mM NADPH and buffer (100 mM potassium phosphate and 10 mM MgCl2, pH 7.5). For the recombinant CYP4A system, recombinant cell membranes containing the expressed CYP4A isoform were mixed on ice with purified OR and b5 at a molar ratio of 1:14:4, and the diluted inhibitor solution at the indicated concentration, 1 mM NADPH and buffer (150 μl final volume) were added. Mixtures containing either microsomes or recombinant proteins were preincubated at 37°C for 10 min. [1-14C]-arachidonic acid (0.4 μCi, 7 nmol) was then added and incubated at 37°C for 30 min. To determine whether inhibition of arachidonic acid oxidation is reversible or irreversible, a two-stage incubation protocol for time-dependent inhibition was carried out. In the first-stage incubation, microsomes (1.5 mg) were incubated at 37°C with 0.1 mM inhibitors either with or without 1 mM NADPH (300 μl final volume). At given time intervals, an aliquot was diluted 10-fold by the addition of a second-stage assay mixture consisting of the same buffer, 0.9 mM NADPH and [1-14C]-arachidonic acid (0.4 μCi, 7 nmol) in a total volume of 0.4 ml. The reactions were continued for 20 min. The reaction was terminated by acidification to pH 3.5 to 4.0 with 2 M formic acid, and the metabolites were extracted with ethyl acetate. The organic extract was evaporated under nitrogen, resuspended in methanol and injected onto the HPLC column. Reverse-phase HPLC was performed on a 5-μm ODS-Hypersil column, 4.6 × 200 mm (Hewlett-Packard, Palo Alto, CA) using a linear gradient ranging from acetonitrile/water/acetic acid (50:50:0.1) to acetonitrile/acetic acid (100:0.1) at a flow rate of 1 ml/min for 30 min. The elution profile of the radioactive products was monitored by a flow detector (In/us System Inc., Tampa, FL). The identity of each metabolite was confirmed by its comigration with an authentic standard. Specific activity in nmol/mg/min was calculated from the added arachidonic acid, and results were generally expressed as the mean ± S.E.M. of the percent of the control activity. IC50 was determined by quantal dose-response analysis.

COX assay.

The effect of the various inhibitors on COX activity was measured using the purified ram seminal vesicles PGH1 synthase (Cayman Chemical Co., Ann Arbor, MI). The purified enzyme (10 units) was incubated with 1 nmol of arachidonic acid in 0.5 ml of incubation buffer (0.1 M Tris-HCl, pH 8, 1 mM EDTA, 2 mM phenol and 1 μM hematin) with or without PPOH (10 and 50 μM), MS-PPOH (15 and 50 μM), DBDD (2 and 20 μM), DDMS (2 and 20 μM), 17-ODYA (5 and 50 μM) and indomethacin (5 μM). Reaction mixtures were incubated in a 37°C shaking-water bath for 10 min before the addition of arachidonic acid and for 15 min thereafter. All samples were run in duplicate. Amounts of PGE2 were determined using a PGE2-EIA Kit (Cayman Chemical Co., Ann Arbor, MI) after 1000-fold dilution with Tris buffer.

Results

Because of the presence of epoxide hydrolase in microsomal preparations (Oliw et al., 1982), EETs are readily converted to their corresponding metabolites, dihydroxyeicosatrienoic acids (DHETs). We therefore considered epoxygenase activity as the sum of EET and DHET formation. Both PPOH and MS-PPOH were designed to target arachidonic acid epoxidation specifically. Addition of PPOH (1–50 μM) decreased microsomal arachidonate epoxygenase activity in a concentration-dependent manner with an IC50 of 9 μM but had almost no effect on ω-hydroxylation (fig.2). Similar results were obtained with MS-PPOH: no effect on microsomal arachidonic acid ω-hydroxylation (20-HETE formation) and a concentration-dependent inhibition of EETs and DHETs formation with an IC50 of 13 μM (data not shown). These results indicate that PPOH and MS-PPOH specifically and potently inhibit renal microsomal-derived epoxidation of arachidonic acid without affecting ω-hydroxylation.

Figure 2
Figure 2

Effect of PPOH on arachidonic acid ω-hydroxylase and epoxygenase activities in rat cortical microsomes. PPOH was dissolved in ethanol (0.5% final concentration) and preincubated with 150 μg of microsomes and 1 mM NADPH for 10 min before the addition of [1-14C]-arachidonic acid (0.4 μCi). Reactions were carried out at 37°C for 30 min. Arachidonic acid metabolites were extracted and separated by HPLC as described in “Materials and Methods.” Results are expressed as percent of control and are the mean ± S.E.M., n = 3. The control activities for arachidonic acid ω-hydroxylation (formation of 20-HETE) and epoxidation (formation of EET + DHET) were 231 ± 96 and 54 ± 9 pmol/mg/min, respectively.

In order to examine the structure-function relationship of these acetylenic compounds, we tested another aliphatic acetylenic fatty acid, 17-ODYA. The effect of 17-ODYA on renal microsomal ω-hydroxylation and epoxidation of arachidonic acid is shown in figure 3. 17-ODYA was a very potent inhibitor of both ω-hydroxylation and epoxidation of arachidonic acid with similar IC50 values of 7 and 5 μM, respectively.

Figure 3
Figure 3

Effect of 17-ODYA on arachidonic acid ω-hydroxylase and epoxygenase activities in rat cortical microsomes. 17-ODYA was dissolved in ethanol (0.5% final concentration) and preincubated with 150 μg of microsomes and 1 mM NADPH for 10 min before the addition of [1-14C]-arachidonic acid (0.4 μCi). Reactions were carried out at 37°C for 30 min. Arachidonic acid metabolites were extracted and separated by HPLC as described in “Materials and Methods.” Results are expressed as percent of control and are the mean ± S.E.M., n = 3. The control activities for arachidonic acid ω-hydroxylation (formation of 20-HETE) and epoxidation (formation of EET + DHET) were 231 ± 96 and 54 ± 9 pmol/mg/min, respectively.

In addition to these acetylenic compounds, we also examined some dibromo-olefinic fatty acids (DBDD, DPMS and DDMS). Addition of DDMS to the incubation mixture of renal microsomes caused a concentration-dependent inhibition of ω-hydroxylase activity with an IC50 of 2 μM, but it caused only a weak inhibition of epoxygenase activity with an IC50 of 60 μM (fig.4). These results indicate that DDMS is a specific and potent inhibitor of microsomal arachidonic acid ω-hydroxylation. Both DDMS and DBDD demonstrated a pattern of inhibition similar to that of DPMS with different potencies. The IC50 values for all of inhibitors are summarized in table 1.

Figure 4
Figure 4

Effect of DDMS on arachidonic acid ω-hydroxylase and epoxygenase activities in rat cortical microsomes. DDMS was dissolved in ethanol (0.5% final concentration) and preincubated with 150 μg of microsomes and 1 mM NADPH for 10 min before the addition of [1-14C]-arachidonic acid (0.4 μCi). Reactions were carried out at 37°C for 30 min. Arachidonic acid metabolites were extracted and separated by HPLC as described in “Materials and Methods.” Results are expressed as percent of control and are the mean ± S.E.M., n = 3. The control activities for arachidonic acid ω-hydroxylation (formation of 20-HETE) and epoxidation (formation of EET + DHET) were 231 ± 96 and 54 ± 9 pmol/mg/min, respectively.

The specificity of these inhibitors was further examined by using recombinant CYP4A isoforms. We have recently demonstrated that the baculovirus-Sf9 cell-expressed CYP4A2 membranes possess dual catalytic activity: ω-hydroxylation and 11,12-epoxidation (Wang et al., 1996). Preliminary results indicated that CYP4A3 exhibits similar catalytic activities (Nguyen et al., 1997). In contrast, the baculovirus-Sf9 cell-expressed CYP4A1 membranes (Nguyenet al., 1997), as well as other forms of recombinant CYP4A1 (Alterman et al., 1995; Imaoka et al., 1989), exhibit only arachidonic acid ω-hydroxylation activity. Given these characteristics, we examined the effect of PPOH as an epoxygenase inhibitor and that of DDMS as an ω-hydroxylase inhibitor on CYP4A3- and CYP4A1-catalyzed arachidonic acid oxidations. The results are shown in figures 5 and6. PPOH at 30 μM inhibited both CYP4A3-mediated ω-hydroxylation and 11,12-epoxidation of arachidonic acid by 90%. In contrast, PPOH at the same concentration had little effect on CYP4A1-catalyzed ω-hydroxylation of arachidonic acid (8% inhibition). On the other hand, DDMS inhibited both CYP4A1- and CYP4A3-catalyzed arachidonic acid oxidations without differentiating between the two reactions (data not shown).

Figure 5
Figure 5

Representative reverse-phase HPLC elution profiles showing the effect of PPOH on CYP4A1-catalyzed arachidonic acid metabolism. Sf9 cell membranes containing 5 pmol of expressed CYP4A1 were preincubated with 20 pmol of purified b5 and 70 pmol of purified OR without (panel A) or with (panel B) 30 μM PPOH. [1-14C]-arachidonic acid (0.4 μCi; 7 nmol) was added, and the reaction mixture was incubated for an additional 30 min. 20-HETE coeluted with authentic 20-HETE standard at 12 min.

Figure 6
Figure 6

Representative reverse-phase HPLC elution profiles showing the effect of PPOH on CYP4A3-catalyzed arachidonic acid metabolism. Sf9 cell membranes containing 10 pmol of expressed CYP4A3 were preincubated with 40 pmol of purified b5 and 140 pmol of purified OR, without (panel A) or with (panel B) 30 μM PPOH. [1-14C]-arachidonic acid (0.4 μCi; 7 nmol) was added, and the reaction mixture was incubated for an additional 30 min. 20-HETE coeluted with authentic 20-HETE standard at 12 min. The less polar metabolite coeluted with authentic 11,12-EET standard at 17 min.

In order to characterize further the mechanisms of the inhibitory action of these inhibitors, we carried out a two-stage incubation. In the first stage, microsomes were preincubated with either acetylenic (PPOH) or olefinic (DDMS) compounds in the presence and absence of NADPH. Aliquots were then taken at different time-points and added to the incubation reaction, which contained 14C-arachidonic acid. Over a 15-min period in which PPOH was preincubated in the absence of NADPH, there was no time-dependent inhibition of DHET and EET formation (fig. 7A). However, when PPOH was preincubated in the presence of NADPH, there was a rapid, time-dependent decrease in the formation of DHETs and EETs. After a 15-min preincubation, the activity was significantly decreased by 60% (fig. 7A). The same approach was used to test the inhibitory mechanism of DDMS. As shown in figure 7B, neither preincubation time nor the presence of NADPH affected the degree of inhibition by DDMS.

Figure 7
Figure 7

Time-dependent inhibition of renal cortical microsomal epoxygenase activity by PPOH and ω-hydroxylase activity by DDMS. Reaction mixtures containing 1.5 mg of renal cortical microsomal protein and either 50 μM PPOH (panel A) or 20 μM DDMS (panel B) in the presence (▪) and absence (□) of 1 mM NADPH were preincubated for 1, 2, 5, and 15 min at 37°C. The respective controls were microsomes and ethanol in the same preincubation condition. An aliquot of reaction mixtures was then added to test tubes (10-fold dilution) containing [1-14C]-arachidonic acid (0.4 μCi), buffer and 0.9 mM NADPH. The reactions were carried out for 30 min at 37°C. Results are expressed as percent of control and are the mean ± S.E.M., n = 3.

We further examined the effect of these compounds on COX activity by measuring PGH1 synthase-catalyzed conversion of arachidonic acid to PGE2. The results indicated that whereas this activity was readily inhibited by indomethacin (95% inhibition at 5 μM), it was unaffected by the various compounds tested in this study. DDMS, DBDD, DPMS and 17-ODYA at concentrations up to 20 μM had no effect on COX activity; however, PPOH and MS-PPOH at 50 μM inhibited COX activity by 20 and 40%, respectively. Nevertheless, these concentrations are much above the IC50 for epoxygenase activity, and thus they provide a window of selectivity in differentiating between CYP and COX activities.

Discussion

It is well recognized that the CYP-derived eicosanoids constitute a new member of the arachidonic acid cascade with important implications in the regulation of physiological and pathophysiological processes. These metabolites are formed endogenously in various tissues and exert potent biological effects on cellular functions. Studies of their role in normal and diseased cells and tissues are impeded by the difficulty in selectively targeting their synthesis or their effects, because these metabolites are generated from multiple closely related proteins of the CYP superfamily. Consequently, the development of enzyme inhibitors that target specific isoforms/reactions should aid in the study of their pathophysiological roles.

We have synthesized a series of fatty acid/arachidonic acid analogs and tested their potency and selectivity in inhibiting arachidonic acid epoxidation and ω-hydroxylation reactions in rat renal microsomes. Our study confirms that the widely used, terminal acetylenic 17-carbon aliphatic compound 17-ODYA is a potent but nonselective inhibitor of both arachidonic acid epoxidation and ω-hydroxylation in rat renal microsomes. In contrast to 17-ODYA, the other terminal acetylenic compounds, PPOH and MS-PPOH, selectively inhibited microsomal arachidonic acid epoxidation with IC50 values of 9 and 13 μM, respectively, while having no effect on ω-hydroxylations at concentrations up to 50 μM. The major structural difference among these compounds is the presence of a benzene ring moiety in the PPOH derivatives, which suggests that the benzene ring confers selectivity toward the epoxidation reaction. To examine this possibility, Mancyet al. (1996) have proposed a model for the active site of CYP2C9, an arachidonate epoxygenase (Rifkind et al., 1995), in which hydrophobic and/or π-π interactions may be important for binding between the benzene ring of substrates and aromatic amino acid residues of the protein. Alternatively, the ω-hydroxylases may have sterically hindered binding sites that do not accommodate aryl moieties. In a result similar to that observed with 17-ODYA, PPOH inhibitory activity in renal microsomes increased with time and required NADPH, which suggests the formation of an NADPH-dependent intermediate that accounts for inactivation of the enzyme. Ortiz de Montellano and Reich (1984) and Helvig et al. (1997) showed that terminal acetylenes are CYP suicide-substrate inhibitors; they can be further oxidized to a ketene moiety, which then results in alkylation and inactivation of the CYP proteins. PPOH may fit in as a suicide-substrate inhibitor. Furthermore, the time dependence and NADPH dependence of PPOH inhibitory activity are consistent with a mechanism-based irreversible inhibitor (Ortiz de Montellano and Reich, 1984; Muerhoff et al., 1989).

The acyclic compounds, i.e., DDMS, DBDD and DPMS, were selective inhibitors of ω-hydroxylation. The rank order of inhibitory potency was DBDD = DDMS > DPMS, which suggests that a carboxylic acid or methyl sulfimide with 12 carbons (DBDD and DDMS) may be the best fit for the active site of the ω-hydroxylase CYP4A isoforms. Indeed, we and others have demonstrated that recombinant CYP4A proteins have a much higher lauric acid ω-hydroxylase activity than an arachidonic acid ω-hydroxylase activity (Wang et al., 1996; Alterman et al., 1995; Imaoka et al., 1989). Modification of the carboxyl group in DBDD to a methyl sulfonate in DDMS did not change the potency or selectivity of the inhibitory activity. This modification may be important for in vivo studies, where blocking the carboxyl group renders the compound resistant to β-oxidation and makes the compound a more effective inhibitor. Alonso-galicia et al. (1997)administered DDMS locally into an isolated perfused renal arteriolar preparation and systemically into anesthetized rats and demonstrated a high selectivity for DDMS in inhibiting 20-HETE formation. However, unlike 17-ODYA and PPOH, these acyclic dibromide derivatives did not exhibit time- and NADPH-dependent inhibitory activity, a result that emphasizes the importance of a terminal acetylenic bond in providing the mechanisms for the enzyme’s inactivation. These experiments also imply that inhibition by DDMS is reversible. Indeed, when microsomes were incubated with DDMS or DBDD, inhibition of 20-HETE formation could be washed out (data not shown).

The dual catalytic activity of the recombinant CYP4A2/CYP4A3 proteins as ω-hydroxylases and epoxygenases provides a means for examining whether the inhibitors distinguish between these two reactions. The results showed that PPOH caused a significant inhibition of CYP4A3-catalyzed ω-hydroxylation and 11,12-epoxidation of arachidonic acid but had no effect on CYP4A1-dependent ω-hydroxylase activity; this suggests that PPOH inhibitory activity is isoform-specific. In contrast to PPOH, DDMS potently inhibited both CYP4A1- and CYP4A3-catalyzed arachidonate ω-hydroxylation as well as CYP4A3-catalyzed 11,12-epoxidation. Taken together, these results suggest that CYP4A1 and CYP4A2/4A3 may have similar size or topology of the active site, which allows the binding of common substrates such as lauric and arachidonic acids. Conversely, there may be more space or freedom for the orientation of substrates or inhibitors in the active sites of CYP4A2/4A3 compared with those of CYP4A1. Furthermore, the amino acid residues involved in the binding of substrates and inhibitors may be quite different. In other words, it is possible that the active site of CYP4A1 is more rigid than that of CYP4A2/4A3. Indeed, Bambal et al. have proposed that the active site of CYP4A1 is sterically hindered and rigid around the heme iron or ferryl moiety, which may explain the prominent regioselectivity of CYP4A1-catalyzed ω-hydroxylase activity (Bambal and Hanzlik, 1996) and accounts for the differences between CYP4A1 and CYP4A2/4A3 that we observed in catalytic activity and inhibitor sensitivity.

Previous studies by Capdevila et al. (1988) examined the selectivity and potency of various arachidonic acid analogs in inhibiting CYP-dependent arachidonic acid oxygenases. The results demonstrated that these analogs were quite potent at low μM concentrations in inhibiting rat liver microsomal CYP-dependent oxygenase reactions without affecting ram seminal vesicle COX or soybean lipoxygenase activities at concentrations of up to 100 μM. However, these analogs did not significantly distinguish between the different oxygenase reactions; i.e., they inhibited both epoxidation and ω-hydroxylation of arachidonic acid to the same extent. In the same study, the authors documented the potency and selectivity of two imidazole derivatives, clotrimazole and ketoconazole, in preferentially inhibiting arachidonate epoxygenases (Capdevila et al., 1988). These imidazole derivatives are being used extensively in studies to evaluate the physiological role of arachidonate epoxides, especially as they relate to the control of vascular tone and renal function (Makita et al., 1994;Alkayed et al., 1996; Alonso-galicia et al.,1997; Fulton et al., 1995). However, they do affect many CYP-dependent reactions as well as cellular processes unrelated to CYP (Testa and Jenner, 1981; Alvarez et al., 1992).

Our study describes specific inhibitors that, at least in vitro, can distinguish between CYP-catalyzed arachidonate epoxidation and ω-hydroxylation reactions as well as between CYP4A isoform-catalyzed reactions. Additional studies to examine their potency and specificity in vivo, as well as thorough examination of their selectivity with regard to other CYP-catalyzed reactions, should accompany studies designed to evaluate the role of the CYP-arachidonic acid metabolites in the regulation of renal function and blood pressure.

Acknowledgments

The authors thank Dr. Richard J. Roman (Department of Physiology, Medical College of Wisconsin, Milwaukee, WI) for providing the CYP4A1, 4A2, 4A3 and 4A8 cDNAs.

Footnotes

  • Send reprint requests to: Dr. Michal Laniado Schwartzman, Department of Pharmacology, New York Medical College, Valhalla, NY 10595.

  • ↵1 Supported by NIH grants HLPO134300 and EY06513 (M.L.S.) and DK38226 (J.R.F.) and by a Grant-in-Aid (M.H.W.) from the American Heart Association (#970104).

  • ↵2 Mong-Heng Wang and Elimor Brand-Schieber contributed equally to the development of this research paper.

  • Abbreviations:
    CYP
    cytochrome P450
    EET
    epoxyeicosatrienoic acid
    20-HETE
    20-hydroxyeicosatrienoic acid
    17-ODYA
    17-octadecynoic acid
    PPOH
    6-(2-propargyloxyphenyl)hexanoic acid
    MS-PPOH
    N-methanesulfonyl-6-(2-propargyloxyphenyl)hexanamide
    DDMS
    N-methylsulfonyl-12,12-dibromododec-11-enamide
    DBDD
    12-12-dibromododec-11-enoic acid
    DPMS
    N-methylsulfonyl-15,15-dibromopentadec-14-enamide
    SHR
    spontaneously hypertensive rat
    COX
    cyclooxygenase
    • Received July 31, 1997.
    • Accepted November 7, 1997.

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Table 1

Effect of acetylenic and dibromo olefinic fatty acid analogs on arachidonic acid ω-hydroxylation and epoxidation in rat renal cortical microsomes

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OtherPROSTAGLANDINS, LEUKOTRIENES AND OTHER EICOSANOIDS

Cytochrome P450-Derived Arachidonic Acid Metabolism in the Rat Kidney: Characterization of Selective Inhibitors

Mong-Heng Wang, Elimor Brand-Schieber, Barbara A. Zand, Xuandai Nguyen, John R. Falck, Narayanan Balu and Michal Laniado Schwartzman
Journal of Pharmacology and Experimental Therapeutics March 1, 1998, 284 (3) 966-973;
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