Abstract
Serotonin transporter has a key-role in regulation of serotoninergic function, and is involved in numerous neurodegenerative and psychiatric disorders. To obtain an efficient radioactive ligand allowing the study of this transporter in vitro and in vivo, we synthesized a new diphenyl sulfide derivative,N,N-dimethyl-2-(2-amino-4-methylphenylthio)benzylamine or MADAM. We present here extensive pharmacological characterization of this compound. [3H]MADAM bound to serotonin transporters with a very high affinity in vitro on rat cortical membranes, at least 2 times better than the most commonly used radioactive probes (Kd, 60 pM; Bmax, 543 fmol/mg of protein). Competition studies showed few inhibitory effect of nisoxetine (Ki = 270 nM), no inhibitory effect of desipramine or 1-[2-(diphenylmethoxy) ethyl]-4-(3-phenylpropyl)piperazine (GBR 12935) (Ki >1000 nM), and strong effect of paroxetine (Ki = 0.32 nM) and citalopram (Ki = 1.57 nM). Therefore, MADAM has around 1000-fold better selectivity for the serotonin transporter than for other transporters. Autoradiographic studies both on rat and postmortem human brain slices demonstrated that the distribution of [3H]MADAM parallels the localization of serotonin transporters and is prevented by known inhibitors of them. The high affinity and selectivity of [3H]MADAM for the serotonin transporter show that it is very valuable for studies using in vitro approaches. The high selectivity and low nonspecific binding of [3H]MADAM on the postmortem human brain, together with preliminary in vivo results with [11C]MADAM, is a new argument for future use of this ligand in in vivo studies of the distribution, pharmacology, and pathophysiology of the serotonin transporter in the human brain with positron emission tomography.
The function of serotoninergic systems is highly dependent on the membrane serotonin transporters that actively clear serotonin from the synaptic space. In the brain, these transporters have an exclusively neuronal localization on serotoninergic neurons of the raphe nuclei and their projections in rats (Blakely et al., 1991) and humans (Ramamoorthy et al., 1993). The study of serotonin transporters can therefore provide relevant information on the density of serotoninergic neurons as well as on its functioning. Several reports have shown that both these factors can be changed in several disease situations. It has been shown that the serotonin transporter can decline with age (Pirker et al., 2000; Van Dyck et al., 2000) and in several neurodegenerative disorders such as Parkinson's disease (Chinaglia et al., 1993) and Alzheimer's disease (Tejani-Butt et al., 1995). Decreases in serotonin uptake and/or radioligand binding have also been observed postmortem (Stanley et al., 1982; Leake et al., 1991) as well as in vivo (Malison et al., 1998) in human brains following depression or suicide. Moreover, serotonin transporters are major targets of antidepressant drugs including fluoxetine, sertraline, paroxetine, fluvoxamine, and citalopram. The serotonin transporter is therefore involved in major physiological processes as well as in various neurological and psychiatric disorders. This is the basis for exploration of this target protein to provide better understanding of the mechanisms linked to central nervous system diseases and to help in the diagnosis and treatment of these disorders.
Several compounds labeled with β+ or γ emitters have been developed for in vivo exploration of serotonin transporters by positron emission tomography (PET) and single photon emission tomography (SPET). The PET tracers [11C]McN 5652 and [11C]DASB seem currently the most appropriate ligands allowing in vivo quantification of serotonin transporters in the human brain (Parsey et al., 2000; Ginovart et al., 2001). The cocaine derivatives β-CIT (Brücke et al., 1993; Malison et al., 1998) and nor-β-CIT (Hiltunen et al., 1998) have been used for SPET studies, but neither is selective as they also bind to dopamine transporters. Several derivatives from another chemical family such as 5-chloro-2-((2-((dimethylamino)methyl)phenyl)thio)benzyl alcohol or 403U76 (Ferris et al., 1995), iodo-2-((2-((dimethylamino)methyl)phenyl)thio)benzyl alcohol (Oya et al., 1999), and 2-((2-((dimethylamino)methyl)phenyl)thio)-5-iodophenylamine benzyl alcohol or ADAM (Oya et al., 2000), have recently been described as potent ligands of serotonin transporters. ADAM seems to be the best tracer among these compounds in terms of affinity, selectivity, and in vivo properties for SPET exploration of the serotonin transporter (Choi et al., 2000). We recently described ADAM labeled with11C for PET exploration of serotonin transporters for this purpose (Vercouillie et al., 2001). The in vivo kinetics of [11C]ADAM, however, are not appropriate for the half-life of 11C (20 min), as the equilibrium of specific binding to serotonin transporters is obtained in the primate brain at 2 h postinjection (Halldin et al., 2001a). To obtain a more efficient PET tracer, we recently synthesized a derivative of ADAM,N,N-dimethyl-2-(2-amino-4-methylphenylthio)benzylamine (MADAM), which has a high affinity for the serotonin transporter compared with the dopamine and noradrenaline transporters (Emond et al., 2002). In addition, preliminary in vivo scintigraphy in the nonhuman primate showed early and specific binding of [11C]MADAM to the serotonin transporter (Halldin et al., 2001b). In view of these initial findings, we hypothesized that MADAM could be an efficient ligand both for in vitro and in vivo study of the serotonin transporter. To assess this, we labeled MADAM with 3H and undertook the extensive in vitro pharmacological characterization of [3H]MADAM in rat and human brains.
Materials and Methods
Preparation of Stable and Radiolabeled MADAM
MADAM and its N-desmethylated precursor for labelingN-methyl-2-(2-amino-4-methylphenyl thio)benzylamine were synthesized as previously described (Tarkiainen et al., 2001). The labeling of [3H]MADAM was performed as follows; 700 μg of the precursor N-methyl-2-(2-amino-4-methylphenyl thio)benzylamine diluted in 300 μl of dimethyl formamide was mixed with 150 μl of [3H]methyl-iodide (specific activity, 85 Ci/mmol; Amersham Biosciences AB, Uppsala, Sweden) and heated for 15 min at 90°C. After cooling to room temperature, 300 μl of acetonitrile was added, and the tritiated product was purified by high-performance liquid chromatography using a C18 reverse phase column (μ-Bondapack) and CH3CN/NH4CO2H (45:55) as mobile phase. [3H]MADAM was separated from the precursor and methyl-iodide and obtained with a specific activity of 55 Ci/mmol.
Animals and Drugs
All experiments were conducted on male Wistar rats (Centre d'Elevage R. Janvier, Le Genest St. Isle, France), weighing 250–300 g, in accordance with French law regarding animal experiments. Stable ADAM and PE2I were synthesized as already described by Oya et al. (2000) and Emond et al. (1997), respectively. Natural cocaine was obtained from Coopération Pharmaceutique Française (Melun, France). GBR 12935, nisoxetine, desipramine, and fluoxetine were obtained from RBI Bioblock (Illkirch, France). Paroxetine was obtained from SmithKline Beecham (Nanterre, France), and citalopram was from Lundbeck (Copenhagen, Denmark).
In Vitro Binding Studies
Tissue Preparation.
Rats were sacrificed by decapitation on the day of the assay, and the frontal cortex of each animal was removed on ice and weighed (two rats for each experiment). The tissue was homogenized in 10 volumes of 0.32 M sucrose using an Ultraturrax T25 (Bioblock, Illkirch, France). After centrifugation at 1000gfor 10 min at 4°C, the supernatant was kept, and the pellet was treated as described above. Both supernatants were then pooled and centrifuged at 17,500g for 30 min at 4°C. Twenty volumes of the incubation buffer were added to the pellet, and the mixture was homogenized and centrifuged at 50,000g for 10 min at 4°C. The final pellet was suspended in a minimum volume of the assay buffer, and the protein concentration was measured according to Bradford (1976)using bovine serum albumin as standard.
Saturation Studies.
[3H]MADAM was incubated at concentrations varying between 20 and 1500 pM with 60 of μg protein in a total volume of 1 ml in a Tris-HCl buffer, pH 7.4 (50 mM Tris-HCl, 120 mM NaCl, and 5 mM KCl) for 90 min at 22°C. Nonspecific binding was determined in the presence of 10−6 M paroxetine. Samples were then rapidly filtered through Whatman GF/C fiber filters (Whatman, Clifton, NJ) soaked with 0.05% polyethylenimine (Sigma-Aldrich, St. Quentin-Fallavier, France). The filters were washed twice with 4 ml of cold buffer, and the residual radioactivity was measured in a β counter (LKB 1215 Rackbeta; Perkin Elmer, Courtaboeuf, France) in the presence of 6 ml of scintillator (LKB Optiphase). Results were analyzed with the EBDA RADLIG program (Biosoft, Cambridge, UK).
Competition Studies.
For these studies, 50 pM of [3H]MADAM was incubated with 60 μg of protein in a total volume of 1 ml in the Tris-HCl buffer (50 mM Tris-HCl, 120 mM NaCl, and 5 mM KCl), pH 7.4, for 90 min at 22°C in the presence of different drugs, either MADAM and ADAM at concentrations of 10−8 to 10−13 M or paroxetine, citalopram, GBR 12935, PE2I, desipramine, and nisoxetine at concentrations of 10−5 to 10−10 M. Samples were then treated as described above. Total binding was determined in the absence of any drug, and nonspecific binding was measured in the presence of 10−6 M paroxetine. The IC50 values were determined graphically for each compound, and the Ki values were calculated according to Cheng and Prussoff (1973), as fully competitive inhibition was the assumed mechanism.
In Vitro Autoradiographic Studies
Rat Brains.
Two animals were sacrificed by decapitation, and their brains were removed and immediately frozen at −35°C in cooled isopentane. Twenty-micron coronal sections were cut with a cryostat microtome at different brain levels (Reichert-Jung Cryocut 1800; Leica, Rueil-Malmaison, France), thaw mounted on gelatin microscope slides, and kept at −80°C until use.
For binding studies, sections were incubated for 60 min at 22°C with 500 pM of [3H]MADAM in 100 μl of a phosphate buffer (10.14 mM NaH2PO4, 137 mM NaCl, 2.7 mM KCl, and 1.76 mM KH2PO4), pH 7.4. The nonspecific binding was defined on adjacent sections incubated in the presence of 1 μM paroxetine. Sections were then washed twice for 10 min in the phosphate buffer at 4°C and rinsed for 1 s in distilled water. After drying, sections were exposed to sensitive film (Hyperfilm 3H; Amersham Biosciences AB) for 4 weeks in X-ray cassettes together with standards (3H microscales; Amersham Biosciences AB). After revelation and fixation, films were analyzed using an image analyzer (Biocom, Les Ulis, France) after identifying anatomical regions according to the Paxinos and Watson's atlas (1986).
Human Postmortem Brains.
The human brains used were obtained from clinical autopsy at the National Institute of Forensic Medicine (Karolinska Institutet, Stockholm, Sweden) and handled as previously described (Hall et al., 1998, 2001). The study was approved by the Ethics Committee at Karolinska Institutet and the Swedish Board of Social Welfare. Cryosectioning on whole hemisphere sections was performed as previously described (Hall et al., 1998, 2001). Experiments were performed on 100-μm horizontal sections.
For the autoradiography studies, sections were incubated for 60 min at 22°C with 1 nM of [3H]MADAM in 10 ml of a phosphate buffer (10.14 mM NaH2PO4, 137 mM NaCl, 2.7 mM KCl, and 1.76 mM KH2PO4), pH 7.4. Nonspecific binding was defined on adjacent sections incubated in the presence of excess (10 μM) fluoxetine. Sections were then washed twice for 10 min in cold phosphate buffer and rinsed for 1 s in distilled water. After drying, the sections were exposed to film (Kodak Biomax MR; Amersham Biosciences) for 12 weeks before development (developer: Kodak D19, fixation: Kodak Fixer 3000; Eastman Kodak, Rochester, NY). The autoradiograms were digitized using a Scan Maker E6 high-resolution scanner (Microtek Europe B.V., Rotterdam, The Netherlands) and Adobe PhotoShop 6.5 (Adobe, San Jose, CA).
Results
In Vitro Binding Studies.
The affinity and density of specific [3H]MADAM binding sites were measured by saturation experiments on rat cortical membranes. In our experimental conditions, the nonspecific binding, determined in the presence of 10−6 M paroxetine, was around 15%. The Scatchard transformation of the resulting data (Fig.1) revealed a linear curve suggesting a one-site model (Hill coefficient = 1) with aKd value of 60 ± 9 pM (mean ± S.D. of three independent determinations, each performed in triplicate) and a Bmax value of 543 ± 181 fmol/mg of protein (mean ± S.D.).
The pharmacological profile of specific [3H]MADAM binding in the frontal cortex was studied using drugs known to bind to the serotonin, dopamine, and norepinephrine transporters (Fig. 2; Table 1). The rank order of potency of these drugs was MADAM = ADAM > paroxetine > citalopram ≫ PE2I > nisoxetine ≫ GBR 12935 = desipramine.
Autoradiographic Studies.
As shown on Fig.3 and Table2, the binding of [3H]MADAM to rat brain sections was consistent with the distribution of serotonin transporters in rat brain regions such as the frontal cortex, latero-dorsal thalamus, superior colliculi, and raphe nuclei. Binding was totally abolished in the presence of 1 μM paroxetine (not shown).
In the human postmortem brain sections (Fig.4), very high [3H]MADAM binding was seen in the pineal gland. Moreover, [3H]MADAM binding was concentrated in the basal ganglia (caudate nucleus and putamen), raphe nuclei, and superior colliculi, and slightly less in cortical regions. Excess fluoxetine (10 μM) blocked most of the [3H]MADAM binding, leaving only low nonspecific binding or binding to other sites.
Discussion
Numerous recent studies have disclosed relationships between disturbances in serotoninergic neurotransmission, cerebral sites of action of antidepressant drugs, and behavioral disorders. Imaging of the serotonin transporter, a major element of the function of serotonin systems, could be useful to explain the role of these systems in the pathophysiological processes of these disorders and to improve therapeutic strategies. To date, few radiotracers have had optimal properties to allow in vivo study of the serotonin transporter, due mainly to high in vivo nonspecific binding or inappropriate kinetics. Derivative compounds from the diphenyl sulfide structure (Ferris et al., 1995) have recently been proposed as potent tracers for scintigraphic exploration of the serotonin transporter, in particular iodo-2-((2-((dimethylamino)methyl)phenyl)thio)benzyl alcohol (Oya et al., 1999), ADAM (Oya et al., 2000; Acton et al., 2001), and DASB (Ginovart et al., 2001). Our team recently described the synthesis and evaluation of several new compounds from this chemical family (Emond et al., 2002); among these derivatives, MADAM appeared to be a good candidate because of its high selective binding to the serotonin transporter compared with dopamine and norepinephrine transporters. In addition, preliminary in vivo scintigraphy in monkeys showed that accumulation of [11C]MADAM was rapid and highly specific in brain regions rich in serotonin transporters (Halldin et al., 2001b). Precise understanding of the pharmacological profile of such a radioactive probe, however, is essential for reliable interpretation of data obtained with it. We therefore characterized this profile using [3H]MADAM in vitro. This ligand bound to the serotonin transporters of cortical membranes with very high affinity,Kd around 60 pM, and a meanBmax value of 543 fmol/mg of protein. Our data fitted with the binding of [3H]MADAM to a one-site model, in agreement with results obtained in same experimental conditions with ADAM, a compound with a closely related structure (Choi et al., 2000). It cannot be excluded that [3H]MADAM may bind to multiple sites, as the buffer used (high sodium concentration and Tris) has already be shown to interfere with binding sites, as described for binding of cocaine derivatives to monoamines transporters (Calligaro and Eldefrawi, 1988; Laruelle et al., 1994). A single binding site, however, has already been determined in rat cortical membrane with different ligands of the serotonin transporter such as [3H]paroxetine (Habert et al., 1985), [3H]citalopram (D'Amato et al., 1987), and [125I]β-CIT (Boja et al., 1992). The affinity of [3H]MADAM for the serotonin transporter was at least 2 times greater than described for the most commonly used in vitro radioactive probes such as [3H]paroxetine (Habert et al., 1985), [3H]citalopram (D'Amato et al., 1987), and [125I]β-CIT (Boja et al., 1992), whereas the Bmax was of the same order for [3H]MADAM and other tracers. Competition studies toward [3H]MADAM showed no inhibitory effect of desipramine (norepinephrine transporter) or GBR 12935 (dopamine transporter), a poor inhibitory effect of nisoxetine (norepinephrine transporter) and PE2I (dopamine transporter), and a strong effect of serotonin transporter ligands such as citalopram, paroxetine, and ADAM. This showed that MADAM had around 1000-fold selectivity for the serotonin transporter over the norepinephrine transporter and dopamine transporter, comparable to that of ADAM (Oya et al., 2000) and DASB (Wilson et al., 2000).
In vitro binding studies on cerebral rat slices followed by autoradiographic analysis provided characterization of the distribution of the tracer among brain areas. The results showed widespread [3H]MADAM binding throughout cerebral regions, fitting well with known serotonin transporter localization and serotoninergic innervation (Vergé and Calas, 2000). The highest levels of [3H]MADAM were found in the dorsal raphe, superior colliculi, frontal cortex, and latero-dorsal thalamic nuclei. The very high binding of [3H]MADAM in the dorsal raphe, corresponding to the serotonin transporters localized on serotoninergic cell bodies and in regions of nerve projections, such as the superior colliculi and latero-dorsal thalamic nuclei, is in agreement with previous studies using other serotonin transporter ligands such as [3H]paroxetine (De Souza and Kuyatt, 1987; Hrdina et al., 1990; Hrdina and Vu, 1993) and [3H]citalopram (D'Amato et al., 1987;Hébert et al., 2001). Some discrepancies, however, appeared between the results obtained with [3H]MADAM and these other ligands, e.g., a relatively high binding in the frontal cortex and a relatively low binding in the caudate-putamen. The high binding in the frontal cortex could be due to our choice of a more anterior cut level for quantification (Bregma 3.70 according toPaxinos and Watson, 1986) than in other studies, whereas the low intensity of striatal binding remains unclear. The distribution of [3H]MADAM binding in the human brain as determined by autoradiograms roughly paralleled that of the autoradiographic study in rats. The highest binding density in the brain was found in the superior colliculus and was totally abolished in the presence of fluoxetine. The strong labeling of the pineal gland indicates the presence of serotonin transporters in this structure. Serotonin is a precursor of the pineal gland hormone melatonin, and it has been shown that mammalian pinealocytes contain more 5-hydroxytryptamine than any other cells (Hayashi et al., 1999). To our knowledge, however, there has been no demonstration of serotonin transporters in the pineal gland. Ligands for the serotonin transporter have been shown to label the vesicular monoamine transporters in the pineal gland (Segonzac et al., 1985; Darchen et al., 1989), a property that may be shared with [3H]MADAM. Vesicular monoamine transporters, however, are located in most brain regions (Darchen et al., 1989), and it is therefore unlikely that the exceptional binding of [3H]MADAM in the pineal gland is to a vesicular monoamine transporters. Previous findings have shown high levels of norepinephrine transporters to the pineal gland (Madras and Kaufman, 1994), but this is not the cause of this strong [3H]MADAM binding. Taken together, autoradiographic studies in rat and human brains showed that [3H]MADAM had high specific binding to the serotonin transporter, with low nonspecific binding. In view of in vivo use of MADAM in humans, it would be now necessary to precisely characterize several of its properties such as the lipophilicity, association/dissociation rate, and plasma protein binding.
In conclusion, the high affinity and selectivity of [3H]MADAM for the serotonin transporter show that this ligand is very valuable for further in vitro studies of this transporter with homogenate assays as well as autoradiography, especially in animal models of serotoninergic system disorders. The high selectivity and low nonspecific binding of [3H]MADAM on postmortem human brains, together with preliminary in vivo results obtained with [11C]MADAM in monkey brains (Halldin et al., 2001b), is a new argument for future use of this ligand for in vivo studies of the distribution, pharmacology, and pathophysiology of the serotonin transporter in the human brain with PET.
Acknowledgments
We thank Kerstin Larsson for technical assistance and are grateful for the discussions on human brain neuroanatomy with Dr. Yasmin Hurd.
Footnotes
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This work was supported by Institut National de la Santéet de la Recherche Médicale (University François Rabelais), an INSERM-Medicinska Forskningsradet grant, and by grants from the Swedish Medical Research Council (11640).
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DOI: 10.1124/jpet.102.042226
- Abbreviations:
- PET
- positron emission tomography
- SPET
- single photon emission tomography
- β-CIT
- 2β-carbomethoxy-3β-(4-iodophenyl)-tropane
- 403U76
- 5-chloro-2-((2-((dimethylamino)methyl)phenyl)thio)benzyl alcohol
- ADAM
- 2-((2-((dimethylamino)methyl)phenyl)thio)-5-iodophenylamine
- MADAM
- N,N-dimethyl-2-(2-amino-4-methylphenylthio) benzylamine
- PE2I
- (E)-N-(3-iodoprop-2-enyl)-2β-carbomethoxy-3β-(4′-methylphenyl)nortropane
- GBR 12935
- 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine
- McN 5652
- trans-1,2,3,5,6,10-β-hexahydro-6-[4-(methylthio)phenyl]pyrrolo-[2,1-a]-isoquinoline
- DASB
- 3-amino-4-(2-dimethylaminomethylphenylsulfanyl)benzonitrile
- Received July 25, 2002.
- Accepted September 4, 2002.
- The American Society for Pharmacology and Experimental Therapeutics