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Role of cationic drug-sensitive transport systems at the blood-cerebrospinal fluid barrier in para-tyramine elimination from rat brain
Fluids and Barriers of the CNS volume 15, Article number: 1 (2018)
para-Tyramine (p-TA) is a biogenic amine which is involved in multiple neuronal signal transductions. Since the concentration of p-TA in dog cerebrospinal fluid (CSF) has been reported to be greater than that in plasma, it is proposed that clearance of cerebral p-TA is important for normal function. The purpose of this study was to examine the role of the blood–brain barrier and blood-cerebrospinal fluid barrier (BCSFB) in p-TA clearance from the brain.
In vivo [3H]p-TA elimination from rat cerebral cortex and from CSF was examined after intracerebral and intracerebroventricular administration, respectively. To evaluate BCSFB-mediated p-TA transport, [3H]p-TA uptake by isolated rat choroid plexus and conditionally immortalized rat choroid plexus epithelial cells, TR-CSFB3 cells, was performed.
The half-life of [3H]p-TA elimination from rat CSF was found to be 2.9 min, which is 62-fold faster than that from rat cerebral cortex. In addition, this [3H]p-TA elimination from the CSF was significantly inhibited by co-injection of excess unlabeled p-TA. Thus, carrier-mediated p-TA transport process(es) are assumed to take part in p-TA elimination from the CSF. Since it is known that transporters at the BCSFB participate in compound elimination from the CSF, [3H]p-TA transport in ex vivo and in vitro models of rat BCSFB was examined. The [3H]p-TA uptake by isolated rat choroid plexus and TR-CSFB3 cells was time-dependent and was inhibited by unlabeled p-TA, indicating carrier-mediated p-TA transport at the BCSFB. The p-TA uptake by isolated choroid plexus and TR-CSFB3 cells was not reduced in the absence of extracellular Na+ and Cl−, and in the presence of substrates of typical organic cation transporters. However, this p-TA uptake was significantly inhibited by cationic drugs such as propranolol, imipramine, amantadine, verapamil, and pyrilamine. Moreover, p-TA uptake by TR-CSFB3 cells took place in an oppositely-directed H+ gradient manner. Therefore, this suggested that p-TA transport at the BCSFB involves cationic drug-sensitive transport systems which are distinct from typical plasma membrane organic cation transporters.
Our study indicates that p-TA elimination from the CSF is greater than that from the cerebral cortex. Moreover, it is suggested that cationic drug-sensitive transport systems in the BCSFB participate in this p-TA elimination from the CSF.
para-Tyramine (p-TA) is one of the trace amines derived from tyrosine and present in fermented foods such as cheese [1, 2]. In the brain, p-TA acts as a neuromodulator, which supports neuronal actions by several neurotransmitters such as l-glutamate and norepinephrine [3, 4]. In addition, p-TA binds to trace amine-associated receptor 1, which is a G protein-coupled receptor and is a therapeutic target for schizophrenia . It has been reported that, after activating the receptor, serotonergic and dopaminergic neuronal actions via serotonin receptor 1A and presynaptic dopamine D2 receptor, respectively, are reduced [6,7,8,9,10]. Since p-TA has a variety of roles in neuronal signal transduction, it is important to understand the homeostatic systems governing the p-TA concentration in the brain.
It is considered that the neural concentration of p-TA is maintained by a balance between production and clearance and there are reports that the activity of in vivo blood-to-brain transport of p-TA is low [11, 12]. In addition, Faraj et al.  have shown that the p-TA concentration in the cerebrospinal fluid (CSF) of dogs is approximately 2.6-fold lower than that in plasma although p-TA is produced in the brain. Therefore, it is conceivable that the p-TA clearance from the brain is relatively greater compared with that of p-TA production. Regarding the metabolic pathway of p-TA, it is known to be metabolized to octopamine and p-hydroxyphenylacetate via dopamine β-hydroxylase and monoamine oxidase, respectively . Brain barriers are involved in the clearance of several neural compounds: the blood-brain barrier (BBB), which is formed by brain capillary endothelial cells, directly separates the brain from the circulating blood . In addition, the cerebrospinal fluid (CSF) is separated from the circulating blood by the blood-CSF barrier (BCSFB) composed of choroid plexus epithelial cells . Recent reports have shown that these barriers play a role in brain-to-blood transport of endogenous anionic and cationic compounds such as homovanillic acid and histamine [16, 17]. Therefore, there is a possibility that the BBB and/or BCSFB transport p-TA from the brain to the circulating blood and play a role in the p-TA clearance system in the brain.
These cells express a variety of plasma membrane transporters which contribute to compound transport across the BBB and BCSFB. In rat brain capillary endothelial cells, mRNAs of serotonin transporter [SERT/solute carrier (Slc) 6a4], organic cation transporter 1–3 (OCT1–3/Slc22a1–3), multidrug and toxin extrusion 1–2 (MATE1–2/Slc47a1–2), organic cation/carnitine transporter 1–2 (OCTN1–2/Slc22a4–5), and plasma membrane monoamine transporter (PMAT/Slc29a4) have been reported to be expressed [18, 19]. Among these transporters, it has been demonstrated that PMAT is involved in 1-methyl-4-phenylpyridinium (MPP+) efflux transport at the BBB, at least in part . Regarding the BCSFB, the mRNA expression of these transporters has also been reported . In addition, our previous studies have shown that PMAT and OCT3 are involved in the elimination of histamine and creatinine, respectively, from rat CSF [16, 20]. Taking these reports into consideration, it is possible that several cationic transporters at these brain barriers take part in the clearance of cationic compounds from the brain. It is known that p-TA is a substrate of plasma membrane transporters, such as SERT, OCT3, PMAT, and dopamine transporter (DAT/Slc6a3) [21,22,23,24] and, thus, it is hypothesized that p-TA in the brain is eliminated via these plasma membrane transporters at the brain barriers.
To increase our knowledge of the homeostatic mechanism(s) governing the cerebral p-TA concentration, the purpose of this study was to examine the role of the brain barriers in p-TA clearance from the brain. To examine p-TA elimination across the BBB, we used an intracerebral microinjection technique. To evaluate BCSFB-mediated p-TA efflux transport, in vivo intracerebroventricular administration and ex vivo transport studies using isolated choroid plexus were performed. In addition, the properties of p-TA uptake were examined using an in vitro model of rat BCSFB, conditionally immortalized rat choroid plexus epithelial cells (TR-CSFB3 cells).
Butanol, n [1-14C] ([14C]n-butanol, 2 mCi/mmol), mannitol, d-[1-14C] ([14C]d-mannitol, 55 mCi/mmol), and tyramine hydrochloride, [ring-3,5-3H]-([3H]p-TA, 50 Ci/mmol) were obtained from American Radiolabeled Chemicals (St. Louis, MO, USA). All other reagents were commercially available.
Wistar rats (male, 6-week-old, ~ 160 g) were purchased from Japan SLC (Hamamatsu, Japan) and maintained in a controlled environment.
In vivo technique for evaluating p-TA elimination across the BBB 
Anesthetized rats, obtained by intraperitoneally injecting pentobarbital sodium solution (50 mg/kg), were fixed in a stereotaxic apparatus (SR-5R; Narishige, Tokyo, Japan). Physiological buffer A (0.5 µL; 122 mM NaCl, 25 mM NaHCO3, 10 mM d-glucose, and 10 mM 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethansulfonic acid (HEPES)-NaOH, 3 mM KCl, 1.4 mM CaCl2, 1.2 mM MgSO4, 0.4 mM K2HPO4, pH 7.4) containing [3H]p-TA (120 nCi/0.5 μL, 2.0 μM) and [14C]d-mannitol (6.0 nCi/0.5 μL, 220 μM) was injected into the parietal cortex area two region of the brain over a period of 1 min. [14C]d-Mannitol, a BBB-impermeable marker, was used to normalize the actual injection volume. At a designated time, each rat was decapitated, and the ipsilateral cerebrum was removed. During the procedure, the behavior of rats and abnormal morphology of the brain was monitored, and there was no apparent change in the anesthetized conditions and brain structure. The tissue was dissolved in 2 N NaOH (2 mL) at 55 °C for 3 h and then mixed with 10 mL Hionic-Fluor (PerkinElmer, Boston, MA, USA). The radioactivity was measured in a liquid scintillation counter equipped with an appropriate crossover correction for 3H and 14C (LSC-6101; Hitachi-Aloka Medical, Tokyo, Japan). The percentage of [3H]p-TA remaining in the ipsilateral cerebrum (%) was obtained from Eq. 1.
Lateral ventricular micro-administration 
Rats were anesthetized by intraperitoneally injecting pentobarbital solution (50 mg/kg), and the head was fixed in the SR-5R (Narishige). A hole was drilled in the skull, 1.5 mm to the left and 0.5 mm posterior to the bregma, into which a needle was fixed as a cannula for injection. Then, 10 μL buffer A containing [3H]p-TA (400 nCi) and [14C]d-mannitol (5 nCi), with or without unlabeled 75 mM p-TA, was injected into the left lateral ventricle over a period of 20 s. At designated times, CSF (50 μL) was withdrawn by cisternal puncture and the levels of 3H and 14C in the CSF and injectate were measured in a liquid scintillation counter (LSC-6101; Hitachi-Aloka Medical). The rats exhibited no abnormal behavior during this technique.
The kinetic parameters of this study were obtained using a one-compartmental model (Eq. 2), where C CSF(t), k e,CSF, and V d,CSF are the concentration in CSF at time t, the elimination rate constant from the CSF, and the distribution volume in the CSF, respectively, of either [3H]p-TA or [14C]d-mannitol.
In addition, “C CSF(t)/dose × 100” is the percentage of the residual concentration of the compound in the CSF normalized by the amount of injectate (% of dose/mL CSF). By multiplying k e by V d,CSF, the apparent elimination clearance from the CSF (CL CSF) was obtained.
Transport study using choroid plexus 
Rats were decapitated and the choroid plexus in the lateral ventricles was isolated. After preincubation of the choroid plexus in buffer A for 1 min at 37 °C, a transport reaction was initiated by applying buffer A containing 1.0 μCi [3H]p-TA and 0.05 μCi [14C]n-butanol, a marker of water space in the choroid plexus , in the absence or presence of unlabeled compounds. Na+-free or Cl−-free buffer was prepared by equimolar replacement of NaCl and NaHCO3 with lithium chloride and potassium bicarbonate or that of NaCl, KCl, and CaCl2 with sodium gluconate, potassium gluconate, and calcium gluconate, respectively. At designated times, the uptake buffer was removed, and the choroid plexus was solubilized by adding 3 N KOH. A liquid scintillation cocktail (Hionic-Fluor; PerkinElmer) was added to the sample, and 3H- and 14C-radioactivities were measured using an LSC-6101 (Hitachi-Aloka Medical).
Uptake by conditionally immortalized rat choroid plexus epithelial cells 
TR-CSFB3 cells were cultured at 33 °C as described previously. Kitazawa et al. have determined the apical localization of Na+, K+-ATPase from an immunocytochemical study using TR-CSFB3 cells cultured onto a glass slide . It has also been demonstrated that the apical-to-cell uptake capacity of [3H]l-proline in TR-CSFB3 cells seeded onto a Transwell® was similar to the uptake value of [3H]l-proline in TR-CSFB3 cells seeded onto a culture plate . The cells were plated onto collagen I-coated 24-well culture plates (BD-Biosciences, Franklin Lakes, NJ, USA) at a density of 1.0 × 105 cells/well and cultured for 2 days at 33 °C. At 37 °C, the cells were washed three times with buffer A and 200 μL [3H]p-TA-containing buffer A (0.75 μCi/mL) was applied. Na+- or Cl−-free buffer A was prepared as described in the previous section. To stop the uptake reaction, cells were rinsed three times with 4 °C buffer A. The cells were subsequently solubilized with 1 N NaOH solution and incubated at room temperature for 12 h. After neutralization with 1 N HCl, the cellular protein and [3H]p-TA-derived radioactivity were determined using a detergent-compatible protein assay kit (BIO-RAD, Hercules, CA, USA) and liquid scintillation counting, respectively.
The distribution volume of [3H]p-TA in isolated rat choroid plexus and TR-CSFB3 cells, namely the tissue/medium ratio and cell/medium ratio, respectively, was obtained from the following equations (Eqs. 3, 4).
The equation was fitted using the nonlinear least-squares regression analysis program, MULTI . To examine the initial uptake process, a linear correlation analysis was performed. The coefficient of determination (r 2) of [3H]p-TA uptake by isolated rat choroid plexus from 0.25 min to 1.0 min was found to be 0.981, which was greater than that from 0.25 min to 2.0 min (r 2 = 0.822). This suggested that the initial [3H]p-TA uptake by isolated rat choroid plexus is reflected in the data up to 1 min. Regarding the uptake of [3H]p-TA by TR-CSFB3 cells, the r 2 of the [3H]p-TA uptake from 0.25 min to 2.0 min was calculated as 0.989, which is similar to that of [3H]p-TA uptake by isolated rat choroid plexus from 0.25 min to 1.0 min and is close to 1. This result suggests that the cell/medium ratio at all time points reflects the initial [3H]p-TA uptake process.
The kinetic parameters for p-TA uptake by TR-CSFB3 cells were obtained from Eq. 7:
where V is the uptake rate of p-TA, [S] is the p-TA concentration in buffer, K m is the Michaelis–Menten constant, and K d is the non-saturable transport clearance. The equation was fitted using the MULTI program . The kinetic parameters are presented as the mean ± standard deviation (S.D.). Other data represent the mean ± standard error of the mean (S.E.M.). The statistical significance of differences between the means was determined using the unpaired Student’s t test for two groups and one-way analysis of variance followed by Dunnett’s test for more than three groups.
Evaluation of p-TA elimination from rat cerebral cortex
The time-course of the percentage [3H]p-TA remaining in rat ipsilateral cerebrum at 5, 10, 20, and 40 min after micro-administration into the parietal cortex area 2 is shown in Fig. 1a. There was no significant difference between the values at 5, 10, 20, and 40 min (p = 0.143), although a tendency for a time-dependent decrease was observed. As a reference value, the half-life (t 1/2) of the percentage of cerebral [3H]p-TA remaining after microinjection into the cerebral cortex was calculated to be 178 ± 68 min.
In vivo p-TA elimination from rat CSF
Figure 1b shows the time profile of “C CSF(t)/dose × 100” values of [3H]p-TA and [14C]d-mannitol after intracerebroventricular injection. The residual concentration in CSF of [3H]p-TA at 1.0, 1.5, and 2.0 min was significantly lower than that of [14C]d-mannitol. [3H]p-TA was eliminated from the CSF with a t 1/2 of 2.85 ± 0.83 min, which is 3.0-fold faster than the t 1/2 of [14C]d-mannitol. From the V d,CSF and k e,CSF values of [3H]p-TA (V d,CSF, 159 ± 16 μL/rat; k e,CSF, 2.43 × 10−1 ± 0.72 × 10−1 min−1), the CL CSF of [3H]p-TA was found to be 38.6 ± 12.0 μL/rat. The kinetic parameters for [14C]d-mannitol, V d,CSF, k e,CSF, and CL CSF, were calculated to be 135 ± 11 μL/rat, 8.07 × 10−2 ± 6.09 × 10−2 min−1, and 10.9 ± 8.3 μL/rat, respectively. To examine the possible contribution of carrier-mediated p-TA elimination system(s) from the CSF, the effect of unlabeled excess p-TA on the concentration ratio of [3H]p-TA and [14C]d-mannitol was examined. The [3H]p-TA/[14C]d-mannitol residual concentration ratio at 2 min was significantly (1.1-fold) increased by co-administration of 75 mM unlabeled p-TA into the rat cerebroventricle compared with that in the control (Fig. 1c), indicating that [3H]p-TA elimination from rat CSF was inhibited by excess unlabeled p-TA.
[3H]p-TA uptake by isolated rat choroid plexus
In order to examine whether p-TA was eliminated from the CSF across the BCSFB, a [3H]p-TA transport study using isolated rat choroid plexus was performed. [3H]p-TA was time-dependently taken up into the isolated rat choroid plexus with an initial uptake rate and an initial distribution volume of 1.19 ± 0.31 μL/(min μL ChP) and 0.895 ± 0.223 μL/μL ChP, respectively (Fig. 2). As shown in Table 1, 10 mM unlabeled p-TA significantly inhibited this [3H]p-TA uptake by 34%. The absence of extracellular Na+ or Cl− did not significantly affect the [3H]p-TA uptake by isolated rat choroid plexus (Table 1), indicating that Na+ and/or Cl−-cotransport systems are not involved in p-TA uptake by the rat choroid plexus. To examine p-TA transport mechanism(s) on the choroid plexus, the compound/drug-sensitivities to [3H]p-TA uptake were examined (Table 1). Several cationic drugs, such as propranolol, pyrilamine, amantadine, imipramine, and verapamil, significantly inhibited [3H]p-TA uptake by the isolated rat choroid plexus by more than 29%. Among typical SLC transporter substrates/inhibitors, choline exhibited 28% inhibition of [3H]p-TA uptake. However, [3H]p-TA uptake by the isolated rat choroid plexus was not significantly altered in the presence of serotonin (a substrate of SERT), MPP+ (a typical substrate of OCT and PMAT), tetraethylammonium (TEA; a typical substrate of OCT, OCTN, and MATE), and p-aminohippurate (PAH; a typical substrate of organic anion transporter, OAT).
Characteristics of [3H]p-TA uptake by TR-CSFB3 cells
To clarify the characteristics of p-TA transport at the BCSFB, a [3H]p-TA transport study using an in vitro model of rat BCSFB, TR-CSFB3 cells, was performed. TR-CSFB3 cells exhibited time-dependent [3H]p-TA uptake with an initial uptake rate and an initial distribution volume of 2.93 ± 0.32 μL/(min mg protein) and 2.25 ± 0.24 μL/mg protein (Fig. 3a, open circles). At 2 min, [3H]p-TA uptake by TR-CSFB3 cells at 4 °C was significantly reduced by 86% (Fig. 3a, closed square). In addition, concentration-dependent p-TA uptake by TR-CSFB3 cells consisted of saturable and non-saturable components with apparent K m, V max and K d values of 3.48 ± 0.83 mM, 7.26 ± 1.61 nmol/(min mg protein), and 9.78 × 10−1 ± 0.66 × 10−1 μL/(min mg protein), respectively (Fig. 3b). Moreover, 10 mM p-TA significantly inhibited the [3H]p-TA uptake by 48% (Table 2). [3H]p-TA uptake by TR-CSFB3 cells was significantly inhibited by more than 30% in the presence of several kinds of cationic drugs/compounds, such as propranolol, imipramine, amantadine, nicotine, desipramine, pyrilamine, and verapamil. In contrast, this [3H]p-TA uptake was not significantly altered by l-carnitine (a typical substrate of OCTN), pyrimethamine (a substrate of MATE), norepinephrine (a substrate of norepinephrine transporter), PAH, serotonin, and cimetidine (a substrate of OCT and MATE). In addition, the [3H]p-TA uptake by TR-CSFB3 cells was significantly increased, but not decreased, by the co-presence of tyrosine (a precursor of p-TA), choline (a substrate of OCT), MPP+, and TEA (Table 2).
The extracellular inorganic anion sensitivity of [3H]p-TA uptake by TR-CSFB3 cells was examined and was found not to be altered in the absence of extracellular Cl−, whereas it was significantly increased, but not decreased, in the absence of extracellular Na+ (Table 2). This result indicates that Na+- and Cl−-cotransporters are not involved in p-TA transport into the choroid plexus. The [3H]p-TA uptake by TR-CSFB3 cells was significantly reduced by 50% at an extracellular pH of 6.0 (Fig. 4a, closed column), and increased 1.8-fold at an extracellular pH of 8.4 (Fig. 4a, hatched column). In order to examine the intracellular pH effect, TR-CSFB3 cells were treated with ammonium chloride, since the intracellular pH is increased by treatment with ammonium chloride (acute), and subsequent removal of ammonium chloride (pretreated) reduces the intracellular pH . An increase in the intracellular pH significantly reduced [3H]p-TA uptake by TR-CSFB3 cells at pH 7.4 and pH 8.4 by 37% and 42%, respectively (Fig. 4b, acute and closed column), compared with respective untreated conditions (Fig. 4b, untreated and open column). In contrast, a reduction in intracellular pH increased [3H]p-TA uptake by TR-CSFB3 cells to 126% and 191% at pH 7.4 and pH 8.4, respectively (Fig. 4b, pretreated and hatched column), relative to the respective untreated conditions.
In this study, p-TA elimination from the brain and CSF was investigated in rats (Fig. 1). To clarify the involvement of the BCSFB in p-TA elimination from the CSF, a p-TA transport study using isolated rat choroid plexus, which forms the BCSFB, was carried out (Fig. 2 and Table 1). Since carrier-mediated transport properties were observed in this study using rat choroid plexus, p-TA transport characteristics were examined in in vitro rat BCSFB model cells (Figs. 3, 4, and Table 2).
The percentage of [3H]p-TA remaining in the ipsilateral cerebrum tended to be reduced in a time-dependent manner (Fig. 1a), although there was no significant difference between the values at examined time points. It is known that p-TA is converted via enzymes in neural cells to several metabolites, such as octopamine . Thus, it is suggested that p-TA and its metabolites are eliminated to a degree from the brain across the BBB. However, this t 1/2, as a reference record (178 min), was 62-fold longer than that of the residual concentration of [3H]p-TA in the CSF (Fig. 1b). These results show that p-TA elimination from the CSF makes a major contribution to cerebral p-TA clearance relative to that from the brain parenchyma or interstitial fluid. In addition, the CL CSF for [3H]p-TA was 3.5-fold higher than that of [14C]d-mannitol, a marker compound for bulk flow of CSF [26, 32]. Taking the inhibitory effect of p-TA elimination from the CSF by excess unlabeled p-TA (Fig. 1c) into consideration, this suggests that carrier-mediated transport system(s), which are distinct from CSF bulk flow, are involved in p-TA elimination from the CSF.
After intracerebroventricular administration, it is possible that [3H]p-TA is distributed to the brain parenchyma and/or taken up into ependymal cells and choroid plexus epithelial cells . It is known that transporters at the BCSFB participate in the elimination of several compounds from the CSF . We have shown that [3H]p-TA was time-dependently taken up into ex vivo isolated rat choroid plexus (Fig. 2) and in vitro choroid plexus epithelial cells, which form the BCSFB (Fig. 3). In addition, this [3H]p-TA uptake was significantly inhibited by unlabeled 10 mM p-TA (Tables 1, 2). Since the initial distribution volume of p-TA was found to be 159 μL (Fig. 1b), the concentration in rat CSF of unlabeled p-TA after a 10 μL intracerebroventricular microinjection of 75 mM unlabeled p-TA was calculated to be 4.7 mM, which is similar to that in the in vitro self-inhibition studies. Therefore, it is suggested that some transport systems at the BCSFB take part in carrier-mediated elimination of p-TA from the CSF.
Since the apical membrane of the choroid plexus faces the [3H]p-TA-containing buffer in the uptake study using isolated choroid plexus, it appears that the characteristics of [3H]p-TA uptake by rat choroid plexus reflects the CSF-to-cell transport direction at the BCSFB. In this study, the choroid plexus from the lateral ventricle was used in the p-TA transport study. Although there are known regional differences in physiological and transport functions between the choroid plexuses from the lateral, third, and fourth ventricles [34, 35], Ogawa et al.  have reported that the in vivo uptake rate which is extrapolated from in vitro benzylpenicillin transport in rat choroid plexus from the lateral ventricle, is in good agreement with that of saturable in vivo elimination of benzylpenicillin from the CSF. p-TA transport across the apical membrane of the isolated rat choroid plexus was found to be 7.14 μL/(min rat) since the total volume of rat choroid plexus has been reported to be 6 μL (7.14 μL/(min rat) = 1.19 μL/μL ChP × 6 μL/rat) . Regarding the polarity of TR-CSFB3 cells after seeding onto a culture plate and glass slide, it has been reported that membrane protein localization onto the plasma membrane of choroid plexus epithelial cells is mostly retained . As the surface area of TR-CSFB3 cells and rat lateral ventricle choroid plexus epithelium has been reported to be 20 cm2/mg protein  and 75 cm2/rat , respectively, the initial p-TA uptake clearance estimated from the uptake study using TR-CSFB3 cells was calculated to be 11.0 μL/(min rat) (= 2.93 μL/(min mg protein) ÷ 20 cm2/mg protein × 75 cm2/rat). This estimated initial p-TA uptake clearance from the transport study using TR-CSFB3 cells is consistent with that using isolated rat choroid plexus. Taking these findings into consideration, there is a high possibility that the characteristics of p-TA uptake by TR-CSFB3 cells reflect the p-TA transport properties of the apical membrane of the BCSFB.
These BCSFB-mediated [3H]p-TA uptake clearance values obtained from the uptake studies of isolated rat choroid plexus (7.14 μL/(min rat) and TR-CSFB3 cells (11.0 μL/(min rat)) were 18.5 and 28.5% of the in vivo total [3H]p-TA elimination clearance from rat CSF (38.6 μL/(min rat), Fig. 1b). As the elimination clearance of [14C]d-mannitol from rat CSF was found to be 10.9 μL (Fig. 1b), 28.2% of the total [3H]p-TA clearance would reflect the CSF bulk flow and diffusion to the brain parenchyma. As the other pathways for p-TA elimination from the CSF, the remainder of which corresponds to (43.3–53.5%), the incorporation of p-TA into the neural cells facing the cerebroventricles, including the ependymal cells, is a possibility. Further analysis to check the radioactivities in choroid plexus and neural cells surrounding the cerebroventricle could help these cells contribute to p-TA elimination from the CSF. Nevertheless, it is considered that the BCSFB is involved in the carrier-mediated p-TA elimination from the CSF, at least in part, since an inhibitory effect of unlabeled excess p-TA on [3H]p-TA uptake by isolated rat choroid plexus (Table 1) and TR-CSFB3 cells (Table 2) was observed.
p-TA uptake by TR-CSFB3 cells exhibited saturable and non-saturable kinetics (Fig. 3b). The clearance of the saturable process of p-TA transport (V max/K m) was found to be 2.09 μL/(min mg protein), which is 2.1-fold higher than that of the non-saturable process [K d, 0.978 μL/(min mg protein)]. This result indicates that the transporter-mediated process makes a major contribution to apical p-TA transport at the BCSFB. It has been reported that human OCT3 and PMAT accept p-TA as a substrate with a K m of 0.281 and 283 μM, respectively [21, 22]. However, the K m value of p-TA uptake by TR-CSFB3 cells (3.48 mM) was inconsistent with these values. mRNA expression of OCT1–2, OCTN1–2, and MATE in addition to OCT3 and PMAT as typical organic cation transporters has been reported  but no attenuation of [3H]p-TA transport into TR-CSFB3 cells and/or isolated rat choroid plexus was observed in the presence of these transporter inhibitors, such as MPP+, TEA, l-carnitine, pyrimethamine, and cimetidine (Tables 1, 2). In summary, these lines of evidence suggest that typical organic cation transporters which are expressed in the BCSFB are not involved in p-TA transport across the BCSFB. Other plasma membrane transporters for p-TA are known: i.e. several Na+-, Cl−-dependent Slc molecules, such as DAT and SERT. However, in the uptake study using isolated rat choroid plexus and TR-CSFB3 cells, [3H]p-TA uptake was not attenuated in the absence of extracellular Na+ and Cl− (Tables 1, 2). The K m value of human DAT- and SERT-mediated p-TA transport has been reported to be 1.7 and 52.7 μM, respectively [23, 24], which is different from the K m value obtained for p-TA uptake by TR-CSFB3 cells. In addition, [3H]p-TA uptake by both isolated rat choroid plexus and TR-CSFB3 cells was not significantly changed in the presence of serotonin, a substrate of SERT (Tables 1, 2). Consequently, we conclude that typical organic cation transporters and the Na+- and Cl−-dependent Slc family do not play a role in apical p-TA transport at the BCSFB.
We showed that p-TA transport into TR-CSFB3 cells exhibited an oppositely-directed H+-gradient (Fig. 4). Cationic drug transport system(s) in several tissues and blood-central nervous system barriers have been proposed [37,38,39,40,41,42,43]. It has been reported that human intestinal epithelial cells transport several cationic drugs, such as bisoprolol and metoprolol, in an extracellular pH-dependent manner [37, 38]. Our previous reports have shown that nicotine is taken up into rat hepatocytes and lung via unidentified transport system(s) which recognize several cationic drugs and exhibit a H+/substrate antiport behavior [39, 40]. Moreover, it has been shown that H+/substrate antiport system(s) involve blood-to-brain transport across the BBB of cationic compounds and drugs, such as pyrilamine, oxycodone, and nicotine, although the molecular identification of the system(s) has not been reported [41,42,43]. p-TA uptake by isolated rat choroid plexus (Table 1) and TR-CSFB3 cells (Table 2) was significantly inhibited by cationic drugs which also inhibited the uptake of pyrilamine, oxycodone, and nicotine by an in vitro BBB model cell line [41, 42]. Thus, it is suggested that cationic drug-sensitive transport system(s), similar to the systems in the BBB, are present on the apical membrane of the BCSFB and are involved in p-TA elimination across the BCSFB from the CSF.
In patients with Parkinson’s disease and depression, monoamine oxidase inhibitors, such as selegiline, are regularly prescribed. It is widely known that patients who take p-TA-enriched foods exhibit neural side-effects such as migraine when receiving pharmacotherapy with monoamine oxidase inhibitors [44, 45]. As one reason for the above side-effects, the activation of noradrenergic signal transduction has been proposed by monoamine oxidase inhibition and, thus, an increase in the neural p-TA concentration. Many monoamine oxidase inhibitors, including selegiline, are cationic and lipophilic drugs. This study has demonstrated that p-TA elimination across the BCSFB from the CSF is inhibited by cationic and lipophilic compounds (Tables 1, 2). Thus, it is possible that the administration of cationic drugs causes an increase in p-TA in the brain via the inhibition of BCSFB-mediated p-TA elimination and exacerbates neuronal actions induced by excess p-TA. Further studies on the identification of p-TA transport molecule(s) which also recognize cationic drugs are needed, since this could help improve the pharmacotherapy of these patients in addition to increasing our understanding of the role of the BCSFB in homeostasis of p-TA levels in the brain. Moreover, it is considered that our findings about the in vitro characteristics of tyramine transport at the BCSFB (Tables 1, 2), such as inhibition by cationic drugs and promotion by the presence of several compounds (i.e., tyrosine, choline, MPP+, and TEA), are helpful for identifying the responsible molecule(s) for tyramine transport at the BCSFB.
Our study demonstrates the greater contribution of p-TA elimination from the CSF to the clearance of p-TA from the brain parenchyma in vivo. From the transport studies using isolated choroid plexus and TR-CSFB3 cells, p-TA efflux transport at the BCSFB was shown to involve cationic drug-sensitive transport systems. These are distinct from typical plasma membrane organic cation transporters in the BCSFB. This study provides a new view of the role of the BCSFB in homeostasis of trace amines in the brain, including p-TA.
blood-cerebrospinal fluid barrier
- C CSF(t):
concentration in CSF at time t
- k e,CSF :
elimination rate constant from the CSF
- K d :
clearance of non-saturable transport
- K m :
multidrug and toxin extrusion
- MPP+ :
organic cation transporter
organic cation/carnitine transporter
plasma membrane monoamine transporter
the p-TA concentration in buffer
standard error of the mean
conditionally immortalized rat choroid plexus epithelial cells
- V :
- V d,CSF :
distribution volume in the CSF
Borkum JM. Migraine triggers and oxidative stress: a narrative review and synthesis. Headache. 2016;56:12–35.
Ledonne A, Berretta N, Davoli A, Rizzo GR, Bernardi G, Mercuri NB. Electrophysiological effects of trace amines on mesencephalic dopaminergic neurons. Front Syst Neurosci. 2011;5:56.
Youdim MB, Weinstock M. Therapeutic applications of selective and non-selective inhibitors of monoamine oxidase A and B that do not cause significant tyramine potentiation. Neurotoxicology. 2004;25:243–50.
Revel FG, Moreau JL, Gainetdinov RR, Bradaia A, Sotnikova TD, Mory R, et al. TAAR1 activation modulates monoaminergic neurotransmission, preventing hyperdopaminergic and hypoglutamatergic activity. Proc Natl Acad Sci USA. 2011;108:8485–90.
Revel FG, Moreau JL, Pouzet B, Mory R, Bradaia A, Buchy D, et al. A new perspective for schizophrenia: TAAR1 agonists reveal antipsychotic- and antidepressant-like activity, improve cognition and control body weight. Mol Psychiatry. 2013;18:543–56.
Wolinsky TD, Swanson CJ, Smith KE, Zhong H, Borowsky B, Seeman P, et al. The Trace Amine 1 receptor knockout mouse: an animal model with relevance to schizophrenia. Genes Brain Behav. 2007;6:628–39.
Lindemann L, Meyer CA, Jeanneau K, Bradaia A, Ozmen L, Bluethmann H, et al. Trace amine-associated receptor 1 modulates dopaminergic activity. J Pharmacol Exp Ther. 2008;324:948–56.
Xie Z, Miller GM. Beta-phenylethylamine alters monoamine transporter function via trace amine-associated receptor 1: implication for modulatory roles of trace amines in brain. J Pharmacol Exp Ther. 2008;325:617–28.
Bradaia A, Trube G, Stalder H, Norcross RD, Ozmen L, Wettstein JG, et al. The selective antagonist EPPTB reveals TAAR1-mediated regulatory mechanisms in dopaminergic neurons of the mesolimbic system. Proc Natl Acad Sci USA. 2009;106:20081–6.
Leo D, Mus L, Espinoza S, Hoener MC, Sotnikova TD, Gainetdinov RR. Taar1-mediated modulation of presynaptic dopaminergic neurotransmission: role of D2 dopamine autoreceptors. Neuropharmacology. 2014;81:283–91.
Oldendorf WH. Brain uptake of radiolabeled amino acids, amines, and hexoses after arterial injection. Am J Physiol. 1971;221:1629–39.
James JH, Escourrou J, Fischer JE. Blood-brain neutral amino acid transport activity is increased after portacaval anastomosis. Science. 1978;200:1395–7.
Faraj BA, Camp VM, Ansley JD, Scott J, Ali FM, Malveaux EJ. Evidence for central hypertyraminemia in hepatic encephalopathy. J Clin Invest. 1981;67:395–402.
Berry MD. Mammalian central nervous system trace amines. Pharmacologic amphetamines, physiologic neuromodulators. J Neurochem. 2004;90:257–71.
Ohtsuki S, Terasaki T. Contribution of carrier-mediated transport systems to the blood–brain barrier as a supporting and protecting interface for the brain; importance for CNS drug discovery and development. Pharm Res. 2007;24:1745–58.
Usui T, Nakazawa A, Okura T, Deguchi Y, Akanuma SI, Kubo Y, et al. Histamine elimination from the cerebrospinal fluid across the blood-cerebrospinal fluid barrier: involvement of plasma membrane monoamine transporter (PMAT/SLC29A4). J Neurochem. 2016;139:408–18.
Mori S, Takanaga H, Ohtsuki S, Deguchi T, Kang YS, Hosoya K, et al. Rat organic anion transporter 3 (rOAT3) is responsible for brain-to-blood efflux of homovanillic acid at the abluminal membrane of brain capillary endothelial cells. J Cereb Blood Flow Metab. 2003;23:432–40.
Okura T, Kato S, Takano Y, Sato T, Yamashita A, Morimoto R, et al. Functional characterization of rat plasma membrane monoamine transporter in the blood–brain and blood-cerebrospinal fluid barriers. J Pharm Sci. 2011;100:3924–38.
Wakayama K, Ohtsuki S, Takanaga H, Hosoya K, Terasaki T. Localization of norepinephrine and serotonin transporter in mouse brain capillary endothelial cells. Neurosci Res. 2002;44:173–80.
Tachikawa M, Kasai Y, Takahashi M, Fujinawa J, Kitaichi K, Terasaki T, et al. The blood-cerebrospinal fluid barrier is a major pathway of cerebral creatinine clearance: involvement of transporter-mediated process. J Neurochem. 2008;107:432–42.
Chen L, Pawlikowski B, Schlessinger A, More SS, Stryke D, Johns SJ, et al. Role of organic cation transporter 3 (SLC22A3) and its missense variants in the pharmacologic action of metformin. Pharmacogenet Genom. 2010;20:687–99.
Engel K, Wang J. Interaction of organic cations with a newly identified plasma membrane monoamine transporter. Mol Pharmacol. 2005;68:1397–407.
Hilber B, Scholze P, Dorostkar MM, Sandtner W, Holy M, Boehm S, et al. Serotonin-transporter mediated efflux: a pharmacological analysis of amphetamines and non-amphetamines. Neuropharmacology. 2005;49:811–9.
Sitte HH, Huck S, Reither H, Boehm S, Singer EA, Pifl C. Carrier-mediated release, transport rates, and charge transfer induced by amphetamine, tyramine, and dopamine in mammalian cells transfected with the human dopamine transporter. J Neurochem. 1998;71:1289–97.
Kakee A, Terasaki T, Sugiyama Y. Brain efflux index as a novel method of analyzing efflux transport at the blood–brain barrier. J Pharmacol Exp Ther. 1996;277:1550–9.
Ogawa M, Suzuki H, Sawada Y, Hanano M, Sugiyama Y. Kinetics of active efflux via choroid plexus of beta-lactam antibiotics from the CSF into the circulation. Am J Physiol. 1994;266:R392–9.
Suzuki H, Sawada Y, Sugiyama Y, Iga T, Hanano M. Transport of benzylpenicillin by the rat choroid plexus in vitro. J Pharmacol Exp Ther. 1987;242:660–5.
Suzuki H, Sawada Y, Sugiyama Y, Iga T, Hanano M. Transport of cimetidine by the rat choroid plexus in vitro. J Pharmacol Exp Ther. 1986;239:927–35.
Kitazawa T, Hosoya K, Watanabe M, Takashima T, Ohtsuki S, Takanaga H, et al. Characterization of the amino acid transport of new immortalized choroid plexus epithelial cell lines: a novel in vitro system for investigating transport functions at the blood-cerebrospinal fluid barrier. Pharm Res. 2001;18:16–22.
Yamaoka K, Tanigawara Y, Nakagawa T, Uno T. A pharmacokinetic analysis program (multi) for microcomputer. J Pharmacobiodyn. 1981;4:879–85.
Ohta KY, Inoue K, Hayashi Y, Yuasa H. Molecular identification and functional characterization of rat multidrug and toxin extrusion type transporter 1 as an organic cation/H+ antiporter in the kidney. Drug Metab Dispos. 2006;34:1868–74.
Suzuki H, Sawada Y, Sugiyama Y, Iga T, Hanano M. Saturable transport of cimetidine from cerebrospinal fluid to blood in rats. J Pharmacobiodyn. 1985;8:73–6.
Akanuma S, Sakurai T, Tachikawa M, Kubo Y, Hosoya K. Transporter-mediated l-glutamate elimination from cerebrospinal fluid: possible involvement of excitatory amino acid transporters expressed in ependymal cells and choroid plexus epithelial cells. Fluids Barriers CNS. 2015;12:11.
Quay WB. Regional differences in metabolism and composition of choroid plexuses. Brain Res. 1966;2:378–89.
Krunic N, Adamson SL, Coceani F. Differential uptake and catabolism of prostaglandin (PG)E(2) versus PGF(2alpha) in the sheep choroid plexus during development. Brain Res Dev Brain Res. 2000;119:11–9.
Keep RF, Jones HC. A morphometric study on the development of the lateral ventricle choroid plexus, choroid plexus capillaries and ventricular ependyma in the rat. Brain Res Dev Brain Res. 1990;56:47–53.
Fukao M, Ishida K, Horie A, Taguchi M, Nozawa T, Inoue H, et al. Variability of bioavailability and intestinal absorption mechanisms of metoprolol. Drug Metab Pharmacokinet. 2014;29:162–7.
Ishida K, Horie A, Nishimura M, Taguchi M, Fujii N, Nozawa T, et al. Variability of bioavailability and intestinal absorption characteristics of bisoprolol. Drug Metab Pharmacokinet. 2013;28:491–6.
Tega Y, Akanuma S, Kubo Y, Hosoya K. Involvement of the H+/organic cation antiporter in nicotine transport in rat liver. Drug Metab Dispos. 2015;43:89–92.
Tega Y, Yuzurihara C, Kubo Y, Akanuma SI, Ehrhardt C, Hosoya KI. Functional expression of nicotine influx transporter in A549 human alveolar epithelial cells. Drug Metab Pharmacokinet. 2016;31:99–101.
Tega Y, Akanuma S, Kubo Y, Terasaki T, Hosoya K. Blood-to-brain influx transport of nicotine at the rat blood–brain barrier: involvement of a pyrilamine-sensitive organic cation transport process. Neurochem Int. 2013;62:173–81.
Okura T, Hattori A, Takano Y, Sato T, Hammarlund-Udenaes M, Terasaki T, et al. Involvement of the pyrilamine transporter, a putative organic cation transporter, in blood–brain barrier transport of oxycodone. Drug Metab Dispos. 2008;36:2005–13.
Yamazaki M, Fukuoka H, Nagata O, Kato H, Ito Y, Terasaki T, et al. Transport mechanism of an H1-antagonist at the blood–brain barrier: transport mechanism of mepyramine using the carotid injection technique. Biol Pharm Bull. 1994;17:676–9.
Youdim MB, Bakhle YS. Monoamine oxidase: isoforms and inhibitors in Parkinson’s disease and depressive illness. Br J Pharmacol. 2006;147(Suppl 1):S287–96.
Sathyanarayana Rao TS, Yeragani VK. Hypertensive crisis and cheese. Indian J Psychiatry. 2009;51:65–6.
SA contributed to the design of this study, carried out the in vivo experiments, performed data collection and analysis, and drafted the manuscript. YY carried out most of the experiments. YK participated in the coordination of the study. KH took part in writing the manuscript. All authors read and approved the final manuscript.
The authors thank Dr. Tetsuya Terasaki (Tohoku University, Sendai, Japan) for kindly supplying TR-CSFB3 cells and Mr. Hirokazu Shimada (University of Toyama, Toyama, Japan) for help with the in vitro methods used in this study.
The authors declare that they have no competing interests.
Availability of data and materials
The data sets used and/or analyzed during the current study are available from the corresponding author on request.
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Ethics approval and consent to participate
All animal experiments in this study were approved by the Animal Care Committee of the University of Toyama (#A2017PHA-6).
This research was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI [Grant Numbers JP16H05110 and JP16K08365] and the Research Grant from the Smoking Research Foundation.
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