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GASTROINTESTINAL, HEPATIC, PULMONARY, AND RENAL

Discovery and Characterization of Novel Tryptophan Hydroxylase Inhibitors That Selectively Inhibit Serotonin Synthesis in the Gastrointestinal Tract

Lexicon Pharmaceuticals, Inc., The Woodlands, Texas (Q.L., Q.Y., W.S., P.V., W.H., X.-Q.Y., Z.H., W.Y., B.J., R.P., V.C.-G., M.G., E.O., R.B., E.C., K.P., A.W., D.P., A.S., B.Z.); and Lexicon Pharmaceuticals, Inc., Princeton, New Jersey (Z.-c.S.)

Received October 8, 2007; accepted January 9, 2008.

	Abstract

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5-Hydroxytryptamine (serotonin) (5-HT) is a neurotransmitter with both central and peripheral functions, including the modulation of mood, appetite, hemodynamics, gastrointestinal (GI) sensation, secretion, and motility. Its synthesis is initiated by the enzyme tryptophan hydroxylase (TPH). Two isoforms of TPH have been discovered: TPH1, primarily expressed in the enterochromaffin cells of the gastrointestinal tract, and TPH2, expressed exclusively in neuronal cells. Mice lacking Tph1 contain little to no 5-HT in the blood and GI tract while maintaining normal levels in the brain. Because GI 5-HT is known to play important roles in normal and pathophysiology, we set out to discover and characterize novel compounds that selectively inhibit biosynthesis of GI 5-HT. Here, we describe two of a series of these inhibitors that are potent for TPH activity both in biochemical and cell-based assays. This class of compounds has unique properties with respect to pharmacokinetic and pharmacodynamic effects on GI serotonin production. Similar to the Tph1 knockout results, these TPH inhibitors have the ability to selectively reduce 5-HT levels in the murine GI tract without affecting brain 5-HT levels. In addition, administration of these compounds in a ferret model of chemotherapy-induced emesis caused modest reductions of intestinal serotonin levels and a decreased emetic response. These findings suggest that GI-specific TPH inhibitors may provide novel treatments for various gastrointestinal disorders associated with dysregulation of the GI serotonergic system, such as chemotherapy-induced emesis and irritable bowel syndrome.

5-HT is involved in the control and modulation of multiple physiological and psychological processes. In the central nervous system (CNS), 5-HT regulates mood, appetite, and other behavioral functions. In the GI system, where close to 90% of the 5-HT in the body is synthesized and stored, 5-HT plays a prokinetic role in general, and it is an important mediator of sensation (e.g., nausea and satiety) between the GI tract and the brain (Gershon and Tack, 2007). 5-HT is released when EC cells are activated by stimuli, such as distension or chemical signals; the resultant release of 5-HT increases motility of the gut. Conversely, dysregulation of the GI 5-HT signaling system is involved in the etiology of several conditions such as functional gastrointestinal disorders, chemotherapy-induced emesis, and heart valve damage (Andrews et al., 1990; Kulke and Mayer, 1999; Gershon, 2003, 2005). The large number of pharmaceutical agents that block or stimulate 5-HT receptors is indicative of the wide range of medical disorders that have been associated with 5-HT dysregulation (De Ponti, 2004). Direct blockade of 5-HT synthesis through inhibition of TPH was also evaluated with a compound called para-chlorophenylalanine (pCPA) in humans (Koe and Weissman, 1966; Engelman et al., 1967; Alfieri and Cubeddu, 1995). The compound proved effective in treating diarrhea in patients with carcinoid syndrome and emesis induced by chemotherapy (Engelman et al., 1967; Alfieri and Cubeddu, 1995). However, pCPA treatments have also been linked to depression and other alterations in CNS function (Engelman et al., 1967; Sjoerdsma et al., 1970), precluding the development of this agent for therapeutic use.

Based on the above-mentioned observations, we wanted to determine whether the specific loss of 5-HT from GI tissues would have an effect on emesis. We hypothesized that selective reduction of GI 5-HT synthesis could be achieved with inhibitors exhibiting either isoform selectivity or restricted tissue distribution and that selectively targeted inhibition of TPH could potentially exert a therapeutic effect on emesis or other functional gastrointestinal disorders such as irritable bowel syndrome without exerting undesired CNS effects. We show here that mice deficient for Tph1 lack 5-HT in the GI tract, but they have normal 5-HT levels in the brain. We also describe novel, potent TPH inhibitors that deplete 5-HT in the GI tract while not affecting brain 5-HT levels. When administered to animals in a chemotherapy-induced emesis model, one of these TPH inhibitors was able to decrease the emetic response.

	Materials and Methods

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Generation of Tph1 Homozygous Null (–/–) Mice. A Tph1 targeting vector was constructed using the knockout shuttle (KOS) system (Wattler et al., 1999). A KOS clone (pKOS5) and target vector were isolated essentially as described previously (Salojin et al., 2006). This clone spanned 9.2 kilobases of the Tph1 gene, including exons 2 to 4.

In the pKOS5-derived vector, exon 3 (184 base pairs) and surrounding DNA were replaced by the IRES/LacZ/Neo selection cassette (Supplemental Fig. 1A); this vector was linearized and electroporated into Lex-1 embryonic stem cells, which were derived from 129S5/SvEvBrd mice (formerly designated as 129/SvEvBrd). G418/FIAU-resistant clones were selected, and targeted clones were identified and confirmed by Southern analysis (Supplemental Fig. 1B). The sequence of primers used to generate 5' external probes (79/47) and 3' external probes (55/80) was as follows: TPH1-79 (5'-GCTCTTCTAAAACGTCCAGTAG-3'), TPH1-47 (5'-GTCTGAGTAAGATTAAACAATCCG-3'), TPH1-55 (5'-GCATCTTCCCTTTATTCAACC-3'), and TPH1-80 (5'-CTTCATGTGAACTGTACTCTTGG-3'). Embryonic stem cells from two targeted clones were microinjected into (albino) C57BL/6J-Tyr^c-Brd (Zheng et al., 1999) blastocysts to generate chimeric mice, which were then bred to C57BL/6J-Tyr^c-Brd (albino) to allow germline transmission. Heterozygous mice were interbred to produce Tph1-deficient animals (Tph1^tm1Lex). Genotype analysis was performed by conducting quantitative polymerase chain reaction for the Neo gene on mouse tail DNA. Tph1 wild-type (+/+), heterozygous (+/–), and homozygous null (–/–) mice contain zero, one, and two copies of the Neo gene, respectively. Homozygous Tph1 homozygous null mice were born with the expected Mendelian frequency, and they exhibited normal growth with no obvious abnormalities.

Analysis of 5-HT and 5-HIAA Production in Mice. Wild-type, heterozygous, and homozygous null mice were generated in a 129S5/SvEvBrd and C57BL/6J hybrid background. For tissue collection, 1-year-old female mice were anesthetized using isoflurane. Blood was obtained via cardiac puncture, after which animals were immediately euthanized. Blood was collected into a Capiject tube with dipotassium EDTA (Terumo Medical Corp., Elkton, MD). Whole brain, stomach antrum, proximal duodenum, mid jejunum, distal ileum, and proximal and distal halves of the colon were collected. With intestinal tissues, mesenteric fat was removed, the gut lumen was opened, the contents were removed, and the tissue was blotted dry. Tissue wet weight was recorded. Samples were snap-frozen immediately thereafter in liquid nitrogen, and they were stored at –80°C for subsequent 5-HT analysis.

For 24-h urinary 5-HIAA and creatinine analysis, 14-month-old male mice were housed singly, and they were acclimatized to metabolic cages (Nalge Nunc International, Rochester, NY) for 1 week before urine collection. To avoid contamination of spilled food into urine, mice were fed on daily prepared chow paste (1 g of regular chow powder:1 ml of H₂O) in a feeding cup. Urine samples were collected every 24 h for four consecutive days. Urine volumes were recorded, and the samples were analyzed for 5-HIAA and creatinine.

Quantification of 5-HT, 5-HIAA, and Creatinine. Fresh blood was mixed with 9 volumes of lysis solution containing 0.5 M trichloroacetic acid and 0.05 M sodium ascorbate. After rigorous mixing, the samples were filtered through a GF/B 96-well filter plate (Whatman, Clifton, NJ) by centrifugation at 650g for 5 min at 4°C. The filtrates were analyzed for 5-HT by a high-performance liquid chromatography fluorometric method under the following conditions: 1) column: Symmetry C18 (4.6 x 50 mm; Waters, Milford, MA); 2) mobile phase: 97% 100 mM sodium acetate and 3% acetonitrile, pH 3.5; and 3) detection: excitation wavelength, 280 nm; and emission wavelength, 330 nm. For intestinal tissues, frozen samples were homogenized in 4 volumes of homogenization buffer consisting of 0.3 M trichloroacetic acid, 0.1 M sodium acetate, 10 mM EDTA, and 20 mM sodium bisulfate. Brain tissues were homogenized in 1.75 volumes of homogenization buffer; homogenate was centrifuged at 20,000g for 20 min at 4°C, and supernatant was then filtered and 5-HT levels were determined as described above. For urinary 5-HIAA analysis, each sample was diluted 5-fold with a buffer containing 100 mM sodium acetate, pH 3.5, 1 M sodium ascorbate, and 0.5 M EDTA. The diluted samples were centrifuged at 13,000g for 5 min at room temperature, and the supernatant was then filtered as described above. 5-HIAA levels were determined using the high-performance liquid chromatography fluorometric method described above. Creatinine levels were determined using a commercial assay (Creatinine Plus version 2; Roche Diagnostics, Indianapolis, IN).

In Vitro TPH Activity Assays. Human full-length TPH1 and TPH2 were cloned into the expression vector pET24 (Novagen, Madison, WI), expressed in Escherichia coli, and the TPH1 and TPH2 proteins were purified to apparent homogeneity using pterin-based affinity chromatography. Activities of both enzymes were measured using the fluorescence assay as described previously (Moran and Fitzpatrick, 1999). The rat mastoctyoma cell line RBL-2H3, which expresses Tph1 endogenously was obtained from The American Type Culture Collection (Manassas, VA). The cells were seeded at 7000 cells/well in a 96-well plate in complete medium. Cells were treated with TPH1 inhibitors at various concentrations for 3 days. After treatment, media were removed, and the cells were lysed with 0.1 N NaOH; lysates were then filtered and analyzed for 5-HT as described above.

Treatment of Mice with Compounds. All mouse experimental procedures were reviewed and approved by the Lexicon Institutional Animal Care and Use Committee. In general, 14-week-old C57BL/6J-Tyr^c-Brd (albino) male mice were used for all pharmacological experiments. Animals were housed in microisolator cages in a temperature- and light/dark cycle-controlled environment, with access to standard chow diet and water ad libitum. In general, compounds were given at 5 ml/kg by oral gavage twice daily for a period of 3 days. Vehicle controls consisted of polyethylene glycol 400 + 5% dextrose (40:60 ratio) for LP-533401 treatments and 0.1% Tween 20 for all other treatments. Animals were sacrificed 5 h following the last dose, and tissues were collected for 5-HT analyses as described above.

Immunohistochemistry. Mice were euthanized by CO₂, and tissues were fixed by immersion in 10% neutral buffered formalin for 48 h. Tissues were embedded in paraffin, sectioned at 4 µm, mounted on positively charged glass slides (Superfrost Plus; Fisher Scientific, Pittsburgh, PA), stained with hematoxylin and eosin, and mounted with Permount mounting medium (Fisher Scientific) for histopathologic examination. For immunohistochemistry, sections were incubated with primary antibody (rabbit anti-serotonin at 1:4000; S5545; Sigma-Aldrich, St. Louis, MO) for 2 h at room temperature followed by a rinse in phosphate-buffered saline (PBS) before blocking of endogenous peroxidase with hydrogen peroxide in methanol. Sections were rinsed in PBS, and then they were incubated with biotinylated goat anti-rabbit IgG secondary antibody (Vector Laboratories, Burlingame, CA) diluted 1:400 in PBS. Afterward, sections were incubated for 1 h with an avidin-biotin horseradish peroxidase complex (Vector Elite ABC; Vector Laboratories). Diaminobenzidine was used as the chromogenic substrate (Vector DAB Substrate kit; Vector Laboratories), and sections were counterstained with Meyer's hematoxylin. Control sections were incubated with nonspecific primary antibodies (affinity-purified rabbit IgG).

View larger version (18K): [in this window] [in a new window]   Fig. 1. Comparison of 5-HT levels in various tissues, and daily 5-HIAA and creatinine excretion in the urine among Tph1 wild-type (+/+), heterozygous (+/–), and homozygous null (–/–) mice. Error bars are S.E.M. A to C, 5-HT levels in whole blood (A), jejunum (B), and brain (C). The number of animals was wild-type (+/+)(n = 10), heterozygous (+/–)(n = 11), and homozygous null (–/–)(n = 4). *, P < 0.01 versus control (Dunnett's post-test following one-way ANOVA). D to F, 24-h urinary excretion of 5-HIAA (D) and creatinine (E) and ratio of 5-HIAA over creatinine (F). **, P < 0.001 versus control (unpaired Student's t test analysis on each day).

Data Analysis. Data are presented as mean ± S.E.M. Differences between vehicle and compound-treated groups were analyzed by the unpaired Student's t test, or one-way ANOVA followed by Dunnett's multiple comparison test. Unless indicated otherwise, P values less than 0.05 were considered significant.

	Results

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Analysis of 5-HT and 5-HIAA Levels in Tph1 Homozygous Null Mice. We first examined 5-HT levels in various tissues from Tph1-deficient female mice. In such mice, 5-HT levels are reduced by 94% in blood and approximately 99% throughout the gastrointestinal tract (Fig. 1, A and B; Supplemental Table 1), demonstrating that TPH1 is responsible for essentially all 5-HT synthesis there. These observations are consistent with previous findings (Côté et al., 2003; Walther et al., 2003a). It is interesting to note that, in Tph1 heterozygous mice, 5-HT levels are 32% lower in blood and 28 to 47% lower in small and large intestines (Fig. 1, A and B; Supplemental Table 1), indicating that TPH1 is truly the rate-limiting enzyme in the synthesis of GI 5-HT. Furthermore, the loss of 5-HT in whole blood is nearly equivalent to that of the GI tract in both the homozygous and the heterozygous animals, consistent with the well established observation that platelets, without expressing Tph1 or Tph2, take up 5-HT synthesized by the GI tract.

In contrast, brain 5-HT and 5-HIAA levels from Tph1 heterozygous and homozygous null mice showed no statistically significant difference from their wild-type littermates (Fig. 1C; Supplemental Table 1), which is also consistent with previously published data (Walther et al., 2003a). Results obtained from male mice are similar to those from the female mice (data not shown). The normal brain 5-HT and 5-HIAA levels, together with the preserved general health and gastrointestinal function of the Tph1 knockout animals indicates that inhibition of non-neuronal TPH activity represents a potentially safe mechanism of action for drug discovery and development.

Because 5-HIAA is the major metabolite of 5-HT, we compared 24-h urinary output of 5-HIAA in Tph1 wild-type and homozygous null mice (Supplemental Table 2). Total daily 5-HIAA excretion was 80% lower in Tph1 homozygous null mice compared with that of wild-type mice in each of the study days (Fig. 1D; Supplemental Table 2), whereas daily total urinary creatinine excretion was similar between the two groups of animals (Fig. 1E; Supplemental Table 2). After normalization to creatinine output, Tph1-deficient mice still showed 80% reduction in daily 5-HIAA excretion compared with their wild-type littermates (Fig. 1F; Supplemental Table 2). These data demonstrate that approximately 80% of daily urinary 5-HIAA is derived from the metabolism of nonneuronal 5-HT sources. Brain 5-HT, only accounting for 2% of the body's total amount in storage in the mouse, seems to be responsible for 20% of the metabolism, implying a much higher turnover rate in the brain.

Identification of Novel TPH Inhibitors. In an attempt to discover and develop compounds that can inhibit 5-HT synthesis in the gut, we set out to identify novel TPH inhibitors. A high-throughput screen using purified TPH1 was conducted with a library of approximately 200,000 compounds using radiolabeled tryptophan. Several classes of inhibitors were identified, and medicinal chemistry was applied to improve the potency of the compounds (Z.-C. Shi, A. Deyasagayaraj, K. Gu, H. Jin, B. Marinelli, L. Samala, S. Scott, T. Stouch, A. Tunoori, Y. Wang, et al., unpublished data). One of the compounds, LP-533401 (Fig. 2A), was found to inhibit human TPH1 in vitro with an IC₅₀ (concentration causing half of maximal inhibition) value of 0.7 µM (Fig. 3A). It also inhibited purified, recombinant human TPH2 with similar potency (Fig. 3B). In comparison, para-chlorophenylalanine (pCPA) is a much less potent inhibitor, with an IC₅₀ value of approximately 250 µM in the same assay (Fig. 3A). These compounds were also tested in a cell-based assay using the rat mastocytoma cell line RBL-2H3, which expresses Tph1 endogenously. LP-533401 was found to completely inhibit 5-HT production in these cells, with an IC₅₀ value of 0.4 µM (Fig. 3B). pCPA, as expected, showed a significantly less potent IC₅₀ value of 43 µM (Fig. 3C). To improve the efficacy of the compound in vivo, a prodrug was synthesized as an ethyl ester of LP-533401 and designated LP-615819 (Fig. 2B). The prodrug did not inhibit TPH1 in vitro at concentrations up to 40 µM (Fig. 3A). However, in the rat cell line, LP-615819 had about the same potency as LP-533401 (Fig. 3B), indicating that the prodrug had undergone conversion to the active compound in either cells, or cell culture media, or both. Because they have much improved in vitro potency, these compounds were tested in the mouse for 5-HT-lowering effects.

View larger version (7K): [in this window] [in a new window]   Fig. 2. Structures of LP-533401 (A) and LP-615819 (B).

View larger version (12K): [in this window] [in a new window]   Fig. 3. Inhibition of TPH1 and TPH2 activity in enzyme and cell-based assays. A, inhibition of purified human TPH1 (, pCPA; , LP-533401; and , LP-615819). B, inhibition of purified TPH1 and TPH2 by LP-533401 (, TPH1; and , TPH2). C, inhibition of 5-HT production in RBL-2H3 cells (, pCPA; , LP-533401; and , LP-615819). All error bars are S.E.M.

Depletion of Gastrointestinal 5-HT by Novel TPH Inhibitors. We examined in vivo activities of LP-533401 and LP-615819 by administering the compounds into mice through oral gavage for 3 to 4 days, and then we measured the levels of 5-HT in the GI and brain. The use of multiple-day dosing was based on previous reports of slow 5-HT turnover in the GI of the rat after pCPA administration (Koe and Weissman, 1966; Weber, 1970). In one of the studies, LP-533401 was given to mice at either 30 or 90 mg/kg, twice daily, whereas another group was given vehicle only, also twice daily. After six consecutive doses, 5-HT levels in the small intestine (jejunum and ileum) were significantly lower in the LP-533401-treated animals, averaging 55 and 70% reductions at 30 and 90 mg/kg, respectively (Fig. 4A; Supplemental Table 3). 5-HT levels in the colon were also reduced, averaging 24 and 36% reductions at 30 and 90 mg/kg, respectively. In contrast, no significant changes in brain 5-HT levels were observed at either dosage.

View larger version (20K): [in this window] [in a new window]   Fig. 4. Reduction of 5-HT in the intestine and brain of mice after compound treatment. A, effect of vehicle control (white bars) versus LP-533401 at 30 mg/kg (gray bars) and 90 mg/kg (black bars). B, effect of vehicle control (white bars) versus pCPA (gray bars) and LP-615819 (black bars). Data are presented as the mean percentage normalized to vehicle control. Error bars are S.E.M. (n = 5/group).

Because a prior TPH1 inhibitor, pCPA, was shown to lower both intestinal and brain 5-HT with stronger efficacy in the latter, we compared LP-615819, the prodrug of LP-533401, and pCPA side by side in the mouse. Animals were treated twice daily with LP-615819 at 45 mg/kg or pCPA at 90 mg/kg. After 3 days, both compounds had caused reduction of 5-HT levels in the intestine, with LP-533401 showing greater efficacy in the jejunum (Fig. 4B; Supplemental Table 4). More importantly, pCPA, as expected, significantly lowered 5-HT levels in the brain, whereas LP-615819 caused no such effect. In a follow-up study, LP-615819 was given to mice twice daily at three different dose levels (20, 45, and 90 mg/kg) for 3 days. Treatment with LP-615819 caused robust reduction of 5-HT along the entire gastrointestinal tract in a dose-dependent manner (Fig. 5; Supplemental Table 5). The best potency and efficacy with respect to 5-HT reduction was observed in the small intestine, including duodenum, jejunum, and ileum, whereas the least was seen in the stomach antrum (Fig. 5). It is noteworthy that the compound did not reduce brain 5-HT levels significantly, even at the highest dose tested.

View larger version (17K): [in this window] [in a new window]   Fig. 5. Dose-dependent 5-HT reduction in the gastrointestinal tract by LP-615819 in the mouse (, brain; , stomach antrum; ), colon; , ileum; , duodenum; and , jejunum). Data are presented as the mean percentage normalized to vehicle control. Error bars are S.E.M. (n = 5/group).

View larger version (74K): [in this window] [in a new window]   Fig. 6. Immunohistochemistry analysis of intestinal 5-HT from untreated and LP-615819-treated animals. Serotonin-immunoreactive cells are stained brown. Control duodenum (A), jejunum (C), cecum (E), and colon (F). LP-615819-dosed duodenum (B), jejunum (D), cecum (G), and colon (H).

View larger version (26K): [in this window] [in a new window]   Fig. 7. Effect of LP-615819 on cisplatin-induced emesis and intestinal 5-HT levels in the ferret. A, number of retches and vomits. B, combined number of retches and vomits from all LP-615819-treated animals. C, number of emesis periods. D, 5-HT in duodenum. E, 5-HT in jejunum. F, 5-HT in brain. Data are presented as the mean percentage normalized to vehicle control. Error bars are S.E.M. (n = 8/dosage group). *, P < 0.05; **, P < 0.01 versus vehicle control (Dunnett's test following one-way ANOVA).

	Discussion

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Knockout of Tph1 in the mouse demonstrates that the majority of 5-HT synthesis in the GI tract is carried out by TPH1 (Côté et al., 2003; Walther et al., 2003b). Even though enteric neurons are known to express Tph2 (Côté et al., 2003), they apparently contribute to only approximately 1% of total 5-HT content in the GI tract. In the work described here, we compared 5-HT synthesis and 5-HIAA excretion among Tph1 wild-type, heterozygous, and homozygous null mice. Our data are consistent with previous conclusions that deletion of Tph1 leads to 99% loss of 5-HT in the GI tract and 94% reduction in the blood. Furthermore, the significant reduction of 5-HT levels in both the blood and gut of Tph1 heterozygotes indicates that the 5-HT synthesis in the GI tract is influenced by Tph1 copy number.

We have discovered and characterized a series of novel compounds that inhibit both TPH1 and TPH2 in vitro but that selectively lower 5-HT levels in the GI tract. TPH is an intracellular enzyme; therefore, effective inhibitors must cross the plasma membranes to reduce 5-HT synthesis in vivo. pCPA displayed an IC₅₀ value or K_i value of roughly 250 µM against purified, recombinant human TPH1 (the K_i value is approximately equal to the IC₅₀ value here, because the tryptophan concentration was significantly below its K_m value in the assay). In the cell-based assay, pCPA showed an IC₅₀ value of 43 µM, indicating that it was taken up by these cells quite efficiently. LP-533401 showed a K_i value of 0.7 µM against purified TPH1 and an IC₅₀ value of 0.3 µM with RBL-2H3 cells. Both pCPA and LP-533401 (disclosed here) are phenylalanine-based zwitterions, neither of which is expected to be able to diffuse passively across the plasma membrane. We speculate that the two compounds enter the cells through a cognate transporter. The most likely candidates are amino acid transporters located in the plasma membrane. However, the exact mechanism of how pCPA and LP-533401 cross the cellular membrane remains to be determined.

In contrast to pCPA, LP-533401 and LP-615819 do not lower 5-HT levels in the brain when administered orally. Because LP-533401 inhibits TPH2 as potently as it does TPH1 (Fig. 2B), the most likely explanation for its lack of effect on central 5-HT is its inability to cross the blood-brain barrier. Preliminary experiments found that the concentration of LP-533401 in the brain is approximately 1% of that in the plasma after dosing at 10 mg/kg by oral gavage (6.1 nM in the brain versus 485 nM in the plasma at 2 h after administration; Z.-C. Shi, A. Devasagayaraj, K. Gu, H. Jin, B. Marinelli, L. Samala, S. Scott, T. Stouch, A. Tunoori, Y. Wang, et al., unpublished data), indicating that LP-533401 is unable to cross the blood-brain barrier. Furthermore, we examined the effect of LP-533401 on brain 5-HT following i.p. administration of this compound for 5 days at 100 mg/kg, twice daily, and we found that brain 5-HT levels were not altered (vehicle group, 0.66 ± 0.03 µg/g; LP-533401 group, 0.67 ± 0.03 µg/g; P > 0.05, t test). pCPA, which can deplete brain 5-HT quickly and robustly, apparently enters the brain by an unidentified transporter. Although the exact mechanism of the observed differential tissue activity remains to be elucidated, we speculate that the greater molecular mass of LP-533401, compared with pCPA (526.5 versus 199.6 Da), may have prevented its uptake by such a hypothetical transporter.

5-HT released by EC cells after treatment with chemotherapeutic agents is one of the major factors responsible for nausea and vomiting in patients receiving such medications (Andrews et al., 1990). Even though 5-HT3 antagonists are effective in controlling acute nausea and vomiting in the majority of patients, delayed onset nausea and vomiting continues to be a significant issue for patients receiving certain types of chemotherapy (Gregory and Ettinger, 1998; Lindley and Blower, 2000; Schwartzberg, 2007). TPH1 inhibitors alone or in combination with 5-HT3 antagonists may further increase the effectiveness in the control of nausea and vomiting. Consistent with this, pCPA has been tested in a small number of patients for such a purpose, and it was found to be equally effective as the 5-HT3 antagonist ondansetron (Alfieri and Cubeddu, 1995). We tested LP-615819 in the ferret emesis model, and we found that it was able to partially reduce emesis induced by cisplatin. The limited efficacy may be due to the relatively modest (30%) reduction in 5-HT levels observed in the duodenum and jejunum at all three dosages. It was unclear why all three dosages gave nearly the same level of 5-HT reduction. One potential explanation is that 5-HT turnover in the ferret intestine is very slow; therefore, the maximal effect was achieved at the lowest dosage. Another possibility is that LP-615819 had a short-lasting effect, and 5-HT turnover in the ferret is fast enough so that 5-HT in all the groups has rebounded to approximately the same level. Nevertheless, the fact that a similar degree of antiemetic effect was observed at all three dosages is consistent with the corresponding equivalent loss of 5-HT at all dosage levels. Taken together, these data imply that the modest reduction of 5-HT in the upper intestine can lead to alleviation of emesis in the ferret. However, it is still interesting that, given the abundance of 5-HT in the small intestine, a partial antiemetic effect was observed with a limited (30%) reduction of 5-HT. One potential explanation is that the large initial abundance of 5-HT in the GI tract may be masking any observed reduction, caused by LP-615819, in the more physiologically important 5-HT efflux. Nonetheless, our finding that a modest reduction in intestinal 5-HT reduces emesis is cause for further investigations of GI-specific TPH inhibitors for the treatment of nausea and vomiting induced by chemotherapy. However, improved efficacy in emesis reduction will be required for clinical use.

In the periphery, 5-HT participates in several key processes, including vasoconstriction, thrombosis, GI motility, secretion, and nociception. The dysregulation of 5-HT is associated with various maladies, as manifested by the significant number of therapeutic agents targeting the serotonergic system. However, direct inhibition of TPH enzymes has never been seriously explored as a therapeutic approach, due in part to the importance of 5-HT in the brain and to the challenges associated with selective reduction of 5-HT outside the brain. The discovery of two distinct genes, TPH1 and TPH2, responsible for the synthesis of non-neuronal and neuronal 5-HT, respectively, offers the possibility of developing drugs that specifically inhibit one enzyme or the other. However, the generation of such specific inhibitors will be challenging because TPH1 and TPH2 are 71% identical in amino acid sequence and approximately 90% similar in the catalytic domain. The design and synthesis of compounds that cannot cross the blood-brain barrier may offer the best approach in this case.

In summary, we have discovered and characterized two compounds (LP-533401 and LP-615819) that selectively inhibit gastrointestinal 5-HT biosynthesis in animals, leaving brain 5-HT levels unaffected. This tissue-selective profile is probably due to the inability of these compounds to cross the blood-brain barrier, resulting in a restricted tissue distribution in vivo. Moreover, these compounds reduce emesis in a model system. We propose that specific inhibition of gastrointestinal 5-HT will offer therapeutic avenues for a multitude of diseases linked to the dysregulation of peripheral serotonergic pathways, including gastrointestinal diseases such as irritable bowel syndrome.

	Acknowledgements

 
We thank Dr. Melanie Shadoan for helpful discussions on pharmacology studies; Paul Blenzinger and Utpala Daftary for assistance to establish pharmacology protocols in the earlier stage; Mary Jean Sparks for creatinine measurement; Wade Walke and Joe Shaw for assistance with writing and editing; and Yi Hu, Jon Madren, Ellen Huang, and Brenda Gerhardt for the generation of expression constructs for Tph1 and Tph2.

	Footnotes

 
Article, publication date, and citation information can be found at http://jpet.aspetjournals.org.

doi:10.1124/jpet.107.132670.

ABBREVIATIONS: 5-HT, 5-hydroxytryptamine (serotonin); TPH, tryptophan hydroxylase; EC, enterochromaffin; GI, gastrointestinal; CNS, central nervous system; pCPA, para-chlorophenylalanine; KOS, knockout shuttle; 5-HIAA, 5-hydroxyindole acetic acid; PBS, phosphate-buffered saline; ANOVA, analysis of variance; 5-HT3, 5-hydroxytryptamine receptor 3; LP-533401, (2S)-2-amino-3-(4-(2-amino-6-(2,2,2-trifluoro-1-(3'-fluorobiphenyl-4-yl)ethoxy)pyrimidin-4-yl)phenyl)propanoic acid; LP-615819, (2S)-ethyl 2-amino-3-(4-(2-amino-6-(2,2,2-trifluoro-1-(3'-fluorobiphenyl-4-yl)ethoxy)pyrimidin-4-yl)phenyl)propanoic acid; FIAU, 1-2'-deoxy-2'-fluoro-β-D-arabinofuranosyl-5-iodouracil.

The online version of this article (available at http://jpet.aspetjournals.org) contains supplemental material.

Address correspondence to: Dr. Qingyun Liu, Lexicon Pharmaceuticals, Inc., 8800 Technology Forest Place, The Woodlands, TX 77382. E-mail: jliu{at}lexpharma.com

	References

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