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Wyeth Research, Cardiovascular and Metabolic Diseases, Cambridge, Massachusetts
Abstract
Ertiprotafib belongs to a novel class of insulin sensitizers developed for treatment of type 2 diabetes. In insulin-resistant rodent models, ertiprotafib and a close analog lowered both fasting blood glucose and insulin levels and improved glycemic excursion during an oral glucose tolerance test. In addition, treatment of rodents improved lipid profiles, with significantly lowered triglyceride and free fatty acid levels. These results suggested that this therapeutic activity might involve mechanisms in addition to PTP1b inhibition. In this study, we demonstrate that ertiprotafib activates peroxisome proliferator-activated receptor (PPAR) and PPAR at concentrations comparable with those of known agonists of these regulators. Furthermore, it is able to drive adipocyte differentiation of C3H10T1/2 cells, a hallmark of PPAR activation. Livers from ertiprotafib-treated animals showed significant induction of acyl-CoA oxidase activity, probably caused by PPAR engagement in these animals. We also show that ertiprotafib inhibits PTP1b in vitro with nonclassic kinetics at concentrations above its EC50 for PPAR agonism. Thus, the complete mechanism of action for ertiprotafib and related compounds in vivo may involve multiple independent mechanisms, including (but not necessarily limited to) PTP1b inhibition and dual PPAR/PPAR agonism. Ertiprotafib pharmacology and interpretation of clinical results must be seen in light of this complexity.
Increasing prevalence of obesity and type 2 diabetes continues to drive the search for better pharmacologic treatments for dyslipidemia and hyperglycemia (Inzucchi, 2002; Flier, 2004). Thiazolidinediones provide a first opportunity to improve the underlying insulin resistance in patients through activation of the peroxisome proliferator-activated receptor (PPAR)- (PPAR) (Willson et al., 2000; Rosen and Spiegelman, 2001). These agents regulate gene transcription in insulin-sensitive tissues, resulting ultimately in reduced glucose levels in patients through increased utilization in skeletal muscle and decreased de novo synthesis in the liver (Way et al., 2001; Willson et al., 2001). Improvements to thiazolidinedione therapy now focus on improving glycemic and lipid control while avoiding the weight gain and edema seen with these agents (Inzucchi, 2002; Diamant and Heine, 2003; Nesto et al., 2003).
One approach receiving considerable attention is to combine PPAR agonism with activation of PPAR to create a dual agonist (Murakami et al., 1998; Brooks et al., 2001; Cronet et al., 2001; Liu et al., 2001; Lohray et al., 2001). Members of the fibrate class of lipid-lowering drugs act as agonists of PPAR to regulate fatty acid metabolism and ketogenesis in the liver (Willson et al., 2000; Kersten et al., 2000). These potent hypolipidemic agents are used to lower plasma triglyceride levels and raise high-density lipoprotein (HDL) levels. Thus, combining agonism for these receptors in a dual PPAR/ ligand could provide clear advantages to treat the hyperglycemia and dyslipidemia in diabetic patients that have an increased risk for cardiovascular disease (Brooks et al., 2001).
Targeting the protein tyrosine phosphatase PTP1b also provides an opportunity to improve insulin sensitivity without the weight gain seen with current PPAR activators. Genetically deficient PTP1b knockout mice remain healthy with sustained phosphorylation of the insulin receptor, which results in profound insulin sensitivity with improved glucose tolerance, and lower levels of circulating insulin (Elchebly et al., 1999; Klaman et al., 2000). Moreover, these mice have lower adiposity and are resistant to weight gain because of their increased sensitivity to leptin (Cheng et al., 2002; Zabolotny et al., 2002). In addition, mice treated with PTP1b antisense oligonucleotides show increased insulin-dependent signaling, resulting in blood glucose normalization and improved insulin sensitivity (Zinker et al., 2002; Gum et al., 2003). Thus, inhibition of PTP1b could prolong insulin receptor phosphorylation, improve insulin action, normalize glucose levels, and reduce adiposity in diabetic patients.
Members of a class of novel arylbenzonaphthothiophenes and arylbenzonaphthofurans have been developed as PTP1b inhibitors and were shown to improve insulin sensitivity in rodents (Wrobel et al., 1999). One compound from these efforts, ertiprotafib, progressed to phase II clinical trials for treatment of type 2 diabetes. However, data from in vivo treatment of rodents with ertiprotafib were inconsistent with PTP1b inhibition as the sole mechanism for these changes. It is noteworthy that bone marrow hypocellularity caused by adipocyte deposition was observed in rats treated with suprapharmacologic doses of ertiprotafib, an indication of possible PPAR activation. Furthermore, treated rats showed moderate dose-related increases in liver weights along with ultrastructural signs of peroxisome proliferation, implying potential PPAR activation (Peterson et al., 2004; Z. Tong and J. Scatina, unpublished observations; L. Casciotti and R. Peterson, unpublished observations). These observations prompted the current investigations into the mechanism of action of ertiprotafib.
In this study, we show that ertiprotafib robustly increases insulin sensitivity in both mouse and rat models of insulin resistance. In addition to effects on hyperglycemia and hyperinsulinemia, ertiprotafib and a close analog also dramatically reduce both serum triglyceride and free fatty acid levels in these insulin-resistant rodent models. In vitro assays indicated the likelihood that multiple independent pathways might contribute to the full pharmacological profile of ertiprotafib. It is noteworthy that ertiprotafib was shown to inhibit PTP1b in a time-dependent, enzyme concentration-dependent manner not associated with classic competitive inhibition. In addition, PTP inhibition in cells occurred at relatively high (above 10 e) concentrations. Further cellular studies indicated that ertiprotafib is at least a dual PPAR and PPAR agonist, with EC50 values for transactivation near 1 e, and is able to induce adipocyte differentiation of fibroblast cells, probably through PPAR. Finally, livers from animals treated with ertiprotafib showed significant induction of the PPAR-dependent enzyme, acyl-CoA oxidase. Taken together, these data indicate that ertiprotafib seems to use a complicated mechanism of action in vivo, involving at least engagement of PPAR and -, in addition to possible PTP1b inhibition, to improve insulin sensitivity and lower lipids.
Materials and Methods
PTP1b Assays. Cell-free assays used recombinant human PTP1b (residues 1eC299 expressed and purified from Escherichia coli) in 96-well plates containing 200 e of dimethyl glutaric acid buffer (50 mM 3,3-dimethyl glutaric acid, ionic strength = 0.15 M, 0.01% Triton X-100, 1 mM EDTA, and 1 mM Tris(2-carboxyethyl)phosphine hydrochloride, pH 7.0) plus 1 mM p-nitrophenyl phosphate substrate and various concentrations of inhibitors. Reactions were initiated by the addition of enzyme. Measuring liberation of p-nitro phenyl at OD405 monitored reaction progress, with IC50 values calculated based on initial rates. Experiments determining time dependence, enzyme concentration dependence, and effects of detergents on inhibition were as described in the figure legends. Cellular assays of PTP1b activity were as described previously (Cromlish et al., 1999) with minor modifications. In brief, PTP1b was cloned into the baculovirus transfer vector pBlueBac4.5 (Invitrogen, Carlsbad, CA), and high titer recombinant viral stocks (4.7 x 108 plaque-forming unit/ml) were generated by the manufacturer (Invitrogen) to infect sf21 cells (Invitrogen) at a multiplicity of infection of 10. Infected cells were harvested by washing and centrifugation using Hanks' balanced salt solution buffered with 15 mM HEPES, pH 7.4. PTP1b activity was then measured in 200 e of Hanks' balanced salt solution containing 5 x 104 cells premixed with inhibitors at various concentrations for 30 min, followed by addition of 1 mM pNPP (final concentration) to initiate the reaction. Reaction progress was monitored after 15 min by measuring OD405.
Plasmid Construction. PPAR and PPAR were cloned from Human Placenta Quick-Clone cDNA (BD Biosciences Clontech, Palo, Alto, CA). PPAR was cloned by nested polymerase chain reaction, first with the primers 5'-CGAGGACACCGGAGAGGGGCGCCAC-3' and 5'-GGGAAATGTTGGCAGTGGCTCAGG-3', followed by the set 5'-TCCGTCGACAAGTCTAGAACCACCATGACCATGGTTGACACAGAG-3' and 5'-GTGGTGGTGGCCCGGGCTAGTACAAGTCCTTGTA-3' to allow insertion into the XbaI/SmaI site of the plasmid pED (Kaufman et al., 1991). PPAR was cloned by polymerase chain reaction into pCR4-TOPO (Invitrogen) using the single set of primers 5'-TACTAGTACCACCATGGTGGACACGGAAAGCCCAC-3' and 5'-TACTAGTTCAGTACATGTCCCTGTAGATCTCCT-3', followed by digestion with SpeI and insertion into the XbaI site of pED. The PPAR response element reporter construct (pGL-3.PPRE) was made using the vector pGL3-promoter (Promega, Madison, WI) to allow for regulated expression of luciferase in a background with the SV40 promoter as described by the manufacturer. Three copies of the common PPAR response element (Willson et al., 2000) were inserted as direct repeats using the following dephosphorylated primers annealed together: 5'-CAGGGGACCAGGACAAAGGTCACGTTCGGGAAGGGGACCAGGACAAGG TCAC GTTCGGGAAGGGGACCAGGACAAAGGTCACGTTCGGGAC-3' and 5'-TCGAGTCCCGAACGTGACCTTTGTCCTGGTCCCCTTCCCGAACGTGACCTTTGTCCTGGTCCCCTTCCCGAACGTGACCTTTGTCCTGGTCCCCTGGTAC-3'. The annealed oligomers were then cut and ligated into the KpnI and XhoI sites of pGL3-promoter, placing this regulatory sequence 16 bp upstream of the SV40 promoter and 248 bp upstream of the luciferase coding sequence.
Transcriptional Activation Assays. CV-1 cells (American Type Culture Collection, Manassas, VA) were plated in 12-well plates 1 day before transfection, grown to 60 to 80% confluence, and cotransfected with either pED.PPAR, pED.PPAR, or pED alone along with pGL-3-PPRE (0.1 e of DNA each) using LipofectAMINE (Invitrogen) according to the manufacturer. Six hours after changing to normal growth medium (DME with 10% FBS), compounds were added and cells were incubated for 40 h, harvested, and assayed for luciferase activity using the Luciferase Assay System (Promega) per the manufacturer's instructions.
Adipocyte Differentiation. C3H10T1/2 Clone 8 cells (American Type Culture Collection) were grown in 100 x 20-mm treated polystyrene cell culture dishes (Corning, Palo Alto, CA) in DME medium with 10% FBS. One day after confluence, cells were treated with compounds in the presence of 200 nM insulin for 2 days. Fresh media and test compounds were added (without insulin) for another 3 days. Accumulation of lipid droplets in cells was determined by staining with the lipophilic dye, Oil Red O (Aldrich Chemical Co., Milwaukee, WI), by washing once with PBS, fixing with 10% formalin for 10 min, washing once with PBS and once with 60% 2-proponal, and incubating with 0.3% Oil Red O in 60% 2-propanol for 15 min. Cells were then quickly washed once with 60% 2-proponal and once with water before visualization and photography.
3T3-L1 Differentiation. 3T3-L1 preadipocytes (American Type Culture Collection) were seeded at a density of 2 x 104 cells/ml (2 x 105 cells/dish) and grown to confluence in DME supplemented with 10% calf serum in 100 x 20-mm treated polystyrene cell culture dishes (Corning). Two days after confluence, media was changed to DME plus 10% FBS, 0.5 mM 3-isobutyl-1-methylxanthine, 0.25 e dexamethasone, and 1 e/ml insulin for 2 days followed by incubation in DME 10% FBS plus 1 e/ml insulin for another 2 days. Finally, cells were incubated in DME with 10% FBS only (no insulin) with fresh media every 2 days until more than 90% were differentiated. Cells were then incubated in serum-free DME overnight before assay.
Phosphorylation Assay. After overnight incubation in serum free medium, 3T3-L1 adipocytes were treated with 10 e ertiprotafib or 10 e vanadate for 30 min, plus 10 nM insulin for an additional 10 min. Cells were washed three times to remove the insulin, and serum free media with compounds were added back for an additional hour to allow for dephosphorylation of the insulin receptor and IRS-1. Cells were then harvested in radioimmunoprecipitation assay buffer with protease inhibitors and 1 mM vanadate, vortexed, and centrifuged. Supernatants were blotted directly with HRP-conjugated anti-phosphotyrosine clone 4G10 (Upstate Biotechnology, Lake Placid, NY), followed by detection with ECL (Amersham Biosciences, Piscataway, NJ).
Glucose Uptake. Differentiated 3T3-L1 adipocytes were incubated in serum-free DME for 2 h, washed with KPH buffer (136 mM NaCl, 4.7 mM KCl, 1.25 mM CaCl2, 1.25 mM MgSO4, and 10 mM HEPES, pH 7.4) and pretreated with DMSO or ertiprotafib in KPH buffer for 30 min. Insulin (100 nM) (or buffer) was then added for 15 min before addition of 2-deoxy-D-[2,6-3H]glucose (Pfizer, New York, NY) at 5 e (1 e藽i/ml) for various times. Glucose transport was stopped by three rapid washes in ice-cold PBS. Cells were solubilized in 0.1% SDS, and incorporated radioactivity was quantified by liquid scintillation.
Animals. Male Ob/ob mice were purchased from The Jackson Laboratory (Bar Harbor, ME) and were acclimated upon arrival before study. They were kept on a 12-h/12-h light/dark cycle and fed Rodent Diet 5001 (for mice and rats) from Purina Mills (Pharma Serv, Framingham, MA). Male Zucker fa/fa rats were purchased from Charles River Laboratories, Inc. (Wilmington, MA) and were also acclimated to a 12-h/12-h light/dark and fed the Rodent Diet 5001. Compounds were dosed orally by gavage in an aqueous suspension of 2% Tween 80 and 0.5% methylcellulose. All experimental work was conducted in accordance with the humane guidelines for ethical and sensitive care of the Institutional Animal Care and Use Committee of the United States National Institutes of Health.
Glucose, Insulin, and Lipid Measurements. Whole blood (5 e) was used for glucose readings via tail nick for measurement using the Ascensia Elite XL glucometer and glucose strips (Bayer Corporation, Elkart, IN) by preloading a strip into the meter and touching the end to a small drop of blood on each tail as instructed by the manufacturer. For insulin measurements, blood was collected by cardiac puncture, centrifuged at 8000 rpm for 10 min, and the serum was collected and stored at -80°C until used. Insulin levels were quantified by enzyme-linked immunosorbent assay using the ultra sensitive rat insulin enzyme-linked immunosorbent assay kit from Crystal Chem. Inc. (Downers Grove, IL) per the manufacturer's instructions. In brief, anti-insulin antibody coated microplates were incubated with 100 e/well of samples and standards at various concentrations in the sample diluent provided for 2 h at 4°C. Wells were then aspirated, washed five times with 300 e of washing buffer (provided), and blotted dry. 100 e of insulin enzyme conjugate was then added to each well, followed by room temperature incubation for 30 min, aspiration, seven washes, and blotting before addition of 100 e/well of enzyme substrate solution. After 40 min at room temperature, reactions were stopped with 100 e/well enzyme reaction stopping solution and absorbance was measured at 450 nm. After subtracting absorbance at 630 nm, insulin concentrations were calculated from the standard curves established in each experiment. Serum triglyceride levels were determined using a kit from Sigma (St. Louis, MO) according to the manufacturer's instructions by mixing 10 e of water, glycerol standards, or samples into 0.8 ml of the free glycerol reagent (prepared according to the manufacturer's instructions) followed by incubation for 15 min at room temperature and reading the initial absorbance at 540 nm. The triglyceride reagent (0.2 ml) was then added in each cuvette, followed by mixing and incubation for an additional 15 min at room temperature. After recording each final absorbance at 540 nm, triglyceride levels were calculated (subtracting water blanks) as instructed. Serum free fatty acid levels were determined by colorimetry using the free fatty acids kit from Wako Chemicals (Richmond, VA). This method measures the nonesterified fatty acids present using acyl-CoA synthetase to produce acyl-CoA, which is then oxidized by added acyl-CoA oxidase, producing hydrogen peroxide. In the presence of peroxidase, the generated hydrogen peroxide condenses 3-methyl-N-ethyl-N-(-hydroxyethyl)-aniline (MEHA) with 4-aminoantipyrine, and the resultant color is measured spectrophotometrically at 550 nm. Sample preparation, assays, and calculations for free fatty acid levels were performed as instructed by the manufacturer.
Oral Glucose Tolerance Test. Food was removed at least 12 h before evaluation of glucose disposal. After a tail vein glucose measurement, animals were allowed to recover before receiving an oral bolus of glucose (2 g/kg). Time points were then collected as indicated using tail vein bleeds for glucose levels as above.
Palmitoyl-CoA Oxidase Assay. Liver samples were excised from rats, snap frozen in liquid nitrogen, and stored at -80°C until processed. Liver microsomes were prepared first by homogenization in a Teflon-glass Potter S mechanical homogenizer with a 5x volume of 50 mM Tris-HCl, pH 7.4, with 0.25 M sucrose, 154 mM potassium chloride, and 1 mM EDTA. Microsomes were then purified by differential ultracentrifugation (Aitio and Vainio, 1976), and the protein content of each microsomal fraction was determined with the BioRad (Hercules, CA) protein assay. Palmitoyl-CoA oxidation was measured with modifications of a method described previously (Gray et al., 1983). In brief, cuvettes contained 50 e palmitoyl-CoA, 0.25 mM NAD+, 0.1 mM coenzyme A, 5 mM dithiothreitol, 1.5 mM KCN, 10 e FAD, 0.01% (w/v) Triton X-100, 0.15 mg of bovine serum albumin, and 0.8 mg of liver homogenate in 1 ml of 50 mM Tris-HCl buffer, pH 7.6. Reference cuvettes had no palmitoyl-CoA. The reaction was monitored every 30 s for 30 min at 340 nm at 37°C in a Hitachi U-3010 Spectrophotometer. Activity was quantified as nanomoles of NADH formed per minute per milligram of homogenate protein using 6.22 cm-1 mM-1 as an extinction coefficient. All reagents were purchased from Sigma.
Results
Ertiprotafib and a close analog, compound 3 (see Fig. 1 for structures), were originally developed as in vitro inhibitors of PTP1b capable of improving insulin sensitivity in mice. Table 1 shows an example of the results after 4 days of treatment with ertiprotafib in the leptin-deficient ob/ob mouse model. Here, 11-week-old male ob/ob mice were placed into two similar groups by weight and fasting blood glucose and then dosed with either vehicle (2% Tween 80 and 0.5% methyl cellulose) or ertiprotafib at 25 mg/kg/day for 4 days. After treatment, mice treated with ertiprotafib had their fasting glucose levels returned to the normal range in the context of markedly reduced insulin levels. Thus, ertiprotafib seemed to increase insulin sensitivity in these mice after short-term treatment. It is noteworthy that serum triglyceride levels were also markedly reduced in these treated animals (see below).
To further test the ability of ertiprotafib to increase insulin sensitivity, male Zucker fa/fa rats were dosed with ertiprotafib or compound 3 at either 25 or 5 mg/kg/day for 14 days. Fasting blood glucose levels were measured, and an oral glucose tolerance test was performed on day 10 of dosing, whereas insulin, triglyceride, and free fatty acid levels were measured at the end of the 14-day dosing. As seen with treatment of ob/ob mice, both compounds seemed to significantly improve glucose metabolism in rats (Table 2 and Fig. 2). At 25 mg/kg/day, these compounds decreased both fasting blood glucose and insulin levels compared with vehicle treated rats (Table 2). Furthermore, both ertiprotafib and compound 3 increased glucose disposal after an oral challenge (Fig. 2). Compound 3 seemed to work slightly better at this dose, consistent with its two-fold greater exposure after oral dosing (data not shown), but neither compound was efficacious at the 5 mg/kg/day dose. It is noteworthy that lipid levels were also reduced in treated animals (Table 2). Both triglyceride and free fatty acid levels were substantially reduced in rats treated with 25 mg/kg/day of either compound. Again, compound 3 may be slightly more potent, with free fatty acids levels reduced even at the 5 mg/kg/day dose of this compound. To summarize, both ertiprotafib and compound 3 seem to be robust agents in improving glucose utilization in fa/fa rats while also decreasing lipid levels in these animals.
Decreased lipid levels (especially free fatty acids) may be unexpected for a pure PTP1b inhibitor (Klaman et al., 2000). It was more telling, as mentioned above, that rats treated with suprapharmacologic doses of ertiprotafib showed signs of PPAR family activation (peroxisome proliferation, adipose deposition in bone marrow) (Peterson et al., 2004). Because engagement of PPAR family members could contribute to the efficacy seen here, we re-examined the actions of ertiprotafib in vitro to gain a more complete understanding of its mechanism(s) of action.
In this study, we see that ertiprotafib does not behave as a simple, competitive inhibitor of PTP1b. Inhibition follows a time-dependent, irreversible mechanism that displays nonclassic kinetics (Fig. 3a and Table 3). It is very revealing that this inhibition was dependent on the concentration of enzyme used in each assay, a hallmark of complex inhibition (Table 3). In addition, IC50 values for this class of compounds in cell-free assays of PTP1b enzymatic activity vary depending on each assay's components and their interactions with these nonpolar compounds (data not shown). For example, adding small amounts of the nonionic detergent, Triton X-100, shifts the inhibition curve with ertiprotafib (Table 3). Similar results have been found for compounds related to this series (Burkey et al., 2002; Johnson et al., 2002). Thus, PTP1b inhibition by ertiprotafib must be understood in the context of compounds with similar, complex behavior (Doman et al., 2002; McGovern et al., 2002).
To define the concentrations required to inhibit PTP1b in the cellular milieu, we first used a simplified cellular assay expressing recombinant PTP1b in the baculovirus system in sf21 insect cells and measuring turnover of pNPP as reported previously (Cromlish et al., 1999). In this assay (Fig. 3b), both vanadate and the known, reversible PTP1b inhibitor compound 33 (see Fig. 1 for structure from Taing et al., 1999) give inhibition constants of 0.1 and 4.5 e, respectively, consistent with literature values (Huyer et al., 1997; Cromlish et al., 1999; Taing et al., 1999). Ertiprotafib, on the other hand, inhibits with an IC50 greater than 20 e (Fig. 3b). Similar results were found for compound 3, with an IC50 greater than 20 e (not shown). As in cell-free assays, inhibition by ertiprotafib (but not the control compounds vanadate and compound 33) in this cellular assay varied with assay components and with time, with greater inhibition seen at lower enzyme levels and later time points (data not shown).
Next, potential effects of ertiprotafib on PTP1b regulation of insulin signaling were investigated in 3T3-L1 cells differentiated into adipocytes by standard procedures (Frost and Lane, 1985). Cells were preincubated with inhibitor for 30 min, pulsed with insulin for 10 min, washed, and compounds were added back for another hour before harvest, lysis, electrophoresis and blotting with anti-phosphotyrosine antibodies. This time after insulin withdrawal allows measurement of the rate of dephosphorylation of the insulin receptor and proximal signaling molecules in the presence of inhibitors. Although no significant difference in phosphorylation of the insulin receptor was seen with either vanadate or ertiprotafib, both treatments did give about a 2-fold increase in tyrosine phosphorylation of the downstream molecule IRS-1 (Fig. 4a). The short incubation period makes it likely that this effect occurs through phosphatase inhibition, presumably PTP1b, although at these concentrations, effects on other phosphatases cannot be ruled out. This increase in IRS-1 phosphorylation did not translate into increased glucose uptake by these cells, however. As seen in Fig. 4b, no increase in glucose uptake by the differentiated 3T3-L1 cells was seen with ertiprotafib either alone or with insulin. Similar results were seen with cultured myocytes (data not shown). Taken together, these assays of phosphatase inhibition and insulin signaling indicate that although ertiprotafib inhibits PTP1b in cells, this inhibition occurs at relatively high concentrations (under the specified assay conditions) and may not provide a full explanation of its in vivo efficacy.
To evaluate whether agonism of PPAR family members might play a role in the pharmacology of ertiprotafib, a reporter system was employed using luciferase as the readout. Three copies of the DNA for the consensus PPAR response element (PPRE) were inserted upstream of the SV40 promoter and luciferase gene (reporter plasmid pGL3). This was cotransfected into CV-1 cells along with expression plasmids for either PPAR or PPAR. Test compounds were then added at various concentrations for 40 h (to allow expression of each PPAR and induced transcription of luciferase) before cell lysis and quantification of luciferase activity. As seen in Fig. 5, ertiprotafib seems to activate transcription through both PPAR and PPAR at concentrations similar to known agonists. Here, ciprofibrate gave dose-dependent stimulation of PPAR driven transcription of luciferase (EC50 of 0.6 ± 0.2 e). Ertiprotafib also seemed to drive PPAR-dependent transcription to the same extent, with an EC50 of 1.4 ± 0.5 e. In Fig. 5b, one sees that ertiprotafib also activates transcription through PPAR (EC50 of 1.1 ± 0.4 e), although the magnitude of the response was less than the known PPAR agonist troglitazone (EC50 of 1.7 ± 0.1 e), indicating partial agonism of this receptor by ertiprotafib. Ertiprotafib activation of each PPAR seems to be direct. Figure 6 shows the results of experiments using ertiprotafib to compete for binding of fluorescent fatty acids to each PPAR. In this study, we see competitive displacement of fatty acid binding to PPAR with an IC50 of 0.5 e (Fig. 6a) and displacement of fatty acid binding to PPAR with an IC50 of 0.6 e (Fig. 6b).
The transactivation of PPAR by ertiprotafib also results in relevant responses in cells, as measured by adipocyte differentiation of the murine fibroblast line C3H/10T 1/2 (Fig. 7). This assay was used in identification of PPAR ligands and has been clearly shown to reflect induction of the adipocyte phenotype in a PPAR-dependent manner (Forman et al., 1995). In these assays, fibroblasts are treated with compounds and insulin for a total of 4 to 6 days, washed, fixed, and stained with oil red to visualize the fat droplets that form as a result of adipogenesis. In Fig. 7, one sees the comparison between control cells treated with DMSO alone (A) and cells treated with the known PPAR agonist rosiglitazone (B), or the test compounds ertiprotafib (C) and compound 3 (D). One can clearly see the increase in cells staining positive for fat droplets with oil red when treated with rosiglitazone (Fig. 7B). Ertiprotafib and compound 3 were evaluated in these same cells and also seemed to drive adipogenesis (Fig. 7, C and D). Therefore, not only does ertiprotafib transactivate PPAR in the reporter gene systems, it also serves as bona fide inducer of adipogenesis in fibroblast cells. In fact, compared with rosiglitazone, a known PPAR agonist, both ertiprotafib and its analog improve glycemic excursion to a similar extent after an oral glucose tolerance test in fa/fa rats (Fig. 8).
Last, one sees evidence for the relevance of PPAR engagement in vivo by ertiprotafib, through induction of a PPAR-responsive enzyme in treated animals (Fig. 9). In this study, CN--insensitive palmitoyl-CoA oxidase activity was measured in the isolated microsomes of liver from animals treated with either ertiprotafib or rosiglitazone versus vehicle-treated and lean control rats. One sees no difference in activity in fa/fa rats treated with either vehicle or rosiglitazone (even compared with lean control rats). Ertiprotafib treatment, however, significantly increased oxidase activity (Fig. 9). Thus, one sees evidence of PPAR engagement by ertiprotafib under conditions in which efficacy is seen.
Discussion
Ertiprotafib was initially targeted as a PTP1b inhibitor for the treatment of type 2 diabetes and progressed as far as phase II clinical trials before its development was discontinued. The present study sought to clarify its mechanism(s) of action to aid in interpretation of these results. In this study, PTP1b inhibition by ertiprotafib was shown to follow nonclassic kinetics; results were dependent on the time of incubation as well as assay components such as enzyme concentration. A common mechanism has recently been described for many of the poorly behaved inhibitors that result from screening efforts (Doman et al., 2002; McGovern et al., 2002). Compounds of this type form higher order aggregates that have been visualized by electron microscopy. Their inhibitory properties are dependent upon this aggregation, resulting in nonclassic kinetics. Two signatures of such inhibition are changes in IC50 values with either a change in enzyme concentration or addition of a small amount of detergent (McGovern et al., 2002; B. Shoichet, unpublished observations). Both phenomena were seen in the characterization of ertiprotafib. This demonstration of poorly behaved kinetics confounds estimates of potency versus PTP1b in vivo. Ertiprotafib did seem here to inhibit PTP1b in cellular assays (including delaying de-phosphorylation of IRS-1 in adipocytes) albeit at relatively high concentrations. Ertiprotafib treatment of either fat or muscle cells did not translate into a short term increase in glucose uptake, although these assays may not be sensitive enough to see a partial effect of PTP1b inhibition. Thus, these data indicated that although PTP1b inhibition probably plays some role in the pharmacology of ertiprotafib, potent inhibition of PTP1b seems an unlikely explanation for its complete pharmacological profile.
The data presented here indicate that (in addition to inhibiting PTP1b) ertiprotafib is at least a dual PPAR and PPAR agonist with EC50 values for transactivation of 1 e. Such activities readily explain the observations with suprapharmacologic doses of these compounds (see above) while also contributing to the pharmacology seen at efficacious doses. The efficacy results presented show that ertiprotafib and its analog, compound 3, lowered plasma glucose levels, reduced insulinemia, lowered serum triglycerides, and lowered free fatty acid levels in rodent models of type 2 diabetes. It is noteworthy that similar results were seen when these same animal models were used in the evaluation of thiazolidinediones (Spiegelman, 1998). Although a PTP1b inhibitor could be expected to decrease glucose, insulin, and triglyceride levels based upon the phenotype of the knockout mice, free fatty acid levels were not different in these animals (Klaman et al., 2000). PPAR ligands, however, are able to lower both serum triglycerides and free fatty acids in rodents (Staels et al., 1998; Chou et al., 2002) and are able to improve insulin sensitivity (Guerre-Millo et al., 2000). Thus, given the increase in acyl-CoA oxidase activity in the livers of treated animals, it seems likely that PPAR agonism (in addition to PPAR agonism and PTP1b inhibition) may contribute to the drop in fatty acid levels seen with ertiprotafib treatment, along with a portion of the glucose and insulin lowering. In fact, the livers of Sprague-Dawley rats treated with ertiprotafib showed widespread up-regulation of genes involved in lipid metabolism, peroxisome proliferation, and fatty acid -oxidation (Peterson et al., 2004). These animals also exhibited increased liver weights and hepatocellular hypertrophy, along with decreased cholesterol and triglyceride levels. Furthermore, many of the genes with increased liver expression after ertiprotafib treatment are known to be PPAR-regulated, including acyl-CoA oxidase, PEX11, and CYP4A1 (Peterson et al., 2004). These animals also showed induction of the PPAR-regulated gene CD36 in ovaries as well as multiple PPAR-dependent genes in fat (R. Peterson, R. Jordan, A. Dorner, unpublished observations). Although these studies were performed at doses of ertiprotafib higher than those needed for efficacy, the results are consistent with the data presented here and indicate that PPAR agonism probably contributes to the pharmacology seen with ertiprotafib. In fact, preliminary experiments indicate that ertiprotafib is able to transactivate gene expression through PPAR as well, with an EC50 of 5 e (C. R. Elcombe, unpublished observations). Because agonism of PPAR can be expected to mediate effects in vivo similar to those shown here (Wang et al., 2003), this nuclear receptor may also contribute to the pharmacology observed with ertiprotafib. What portion each of the targets discussed here (PTP1b, PPAR, PPAR, PPAR) may play in the pharmacology of ertiprotafib, as well as potential contributions from other targets (e.g., RXR), requires further study.
In conclusion, results from both in vitro and in vivo experiments indicate that the improvements in peripheral insulin sensitivity (normalizing plasma glucose while reducing insulin levels) and reductions in hyperlipidemia after treatment with ertiprotafib are probably caused by a combination of mechanisms. These data should inform interpretations from results of clinical trials with ertiprotafib and aid in the search for improved insulin sensitizers.
Acknowledgements
We thank Dr. Zhong-Yin Zhang for compound 33, Drs. Arlene Dietrich, Madelene Antane, Paul Dollings, and Jay Wrobel for ertiprotafib and compound 3, Dr. Clifford Elcombe for fatty acid binding studies, and Richard Maylor for helpful advice and discussion.
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