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Altered tryptophan and alanine transport in fibroblasts from boys with attention-deficit/hyperactivity disorder (ADHD): an in vitro study
Behavioral and Brain Functions volume 7, Article number: 40 (2011)
The catecholaminergic and serotonergic neurotransmitter systems are implicated in the pathophysiology of attention-deficit/hyperactivity disorder (ADHD). The amino acid tyrosine is the precursor for synthesis of the catecholamines dopamine and norepinephrine, while tryptophan is the precursor of serotonin. A disturbed transport of tyrosine, as well as other amino acids, has been found in a number of other psychiatric disorders, such as schizophrenia, bipolar disorder and autism, when using the fibroblast cell model. Hence, the aim of this study was to explore whether children with ADHD may have disturbed amino acid transport.
Fibroblast cells were cultured from skin biopsies obtained from 14 boys diagnosed with ADHD and from 13 matching boys without a diagnosis of a developmental disorder. Transport of the amino acids tyrosine, tryptophan and alanine across the cell membrane was measured by the cluster tray method. The kinetic parameters, maximal transport capacity (V max ) and affinity constant (K m ) were determined. Any difference between the two groups was analyzed by Student's unpaired t-test or the Mann Whitney U test.
The ADHD group had significantly decreased V max (p = 0.039) and K m (increased affinity) (p = 0.010) of tryptophan transport in comparison to controls. They also had a significantly higher V max of alanine transport (p = 0.031), but the Km of alanine transport did not differ significantly. There were no significant differences in any of the kinetic parameters regarding tyrosine transport in fibroblasts for the ADHD group.
Tryptophan uses the same transport systems in both fibroblasts and at the blood brain barrier (BBB). Hence, a decreased transport capacity of tryptophan implies that less tryptophan is being transported across the BBB in the ADHD group. This could lead to deficient serotonin access in the brain that might cause disturbances in both the serotonergic and the catecholaminergic neurotransmitter systems, since these systems are highly interconnected. The physiological importance of an elevated transport capacity of alanine to the brain is not known to date.
Attention-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder with a prevalence in children of about 5-7% worldwide [1, 2]. It is clinically characterized by a persistent pattern of inattention and/or hyperactivity-impulsivity that affect cognitive, behavioural, emotional and social functioning and symptoms may also persist into adulthood [1, 3, 4].
As for many other neurodevelopmental disorders no single etiology of ADHD has been provided, but a number of underlying theories exist. The disorder is highly heritable, based on family, twin and adoption studies , but the genetic architecture of ADHD is suspected to be complex. However, a number of candidate genes have been identified and among these are several genes associated with the catecholaminergic system . Also, a recent study shows that children with ADHD have an increased rate of large copy number variants (CNVs) especially at chromosome 16 , which further support ADHD as a genetic disorder.
Many neuro-imaging studies have identified abnormalities of brain structure and function in ADHD and in particular, a dysfunction of the fronto-subcortical pathways in the brain has been implicated . These pathways control attention and motor behaviour, and it is known that the catecholamines; dopamine and norepinephrine, are vital for their function . Moreover, stimulant agents, such as methylphenidate, amphetamine and atomoxetine, which currently are the most common drugs used for treatment of ADHD, act primarily on the catecholaminergic system. Therefore, the neurotransmitters dopamine and norepinephrine have been implicated in the pathophysiology of ADHD. However, an involvement of serotonin and the serotonergic system in the pathophysiology of ADHD have also regained the researchers' interest during recent years, since there is an interaction between the dopaminergic and serotonergic neurotransmitter systems. It is suggested that serotonin can modulate the activity of dopamine and an alteration in the serotonergic neurotransmission can alter dopamine-mediated behaviour [9, 10]. Still, the relevance of serotonin in ADHD needs to be further explored.
The rate of synthesis of the neurotransmitters dopamine, norepinephrine and serotonin in the central nervous system (CNS) is partly dependent on the brain's availability of precursor amino acids . The amino acid tyrosine is the precursor for the synthesis of dopamine and norepinephrine, while tryptophan is the precursor for the synthesis of serotonin and both amino acids are essential for the brain. Amino acids are polar molecules and are therefore actively transported across cell membranes, like the endothelial cells that constitute a part of the blood brain barrier (BBB), by different amino acid transport systems [12–14]. A competition between amino acids using the same transporters exists [13, 15]. A number of different amino acid transport systems, with different amino acid selectivity, have been identified to date, such as system L, system A, and system ASC .
In order to study amino acid transport properties, in various psychiatric disorders, fibroblast cells are being used as a human experimental model. This model is suggested to be relevant since fibroblasts have a similar expression of amino acid transporters as human brain microvascular endothelial cells (hBME) and express several neuronal specific receptors and enzymes [15–18]. Recent studies have also shown that fibroblast cells can be converted into functional neurons . Moreover, they are easily obtained from both patients and controls, and in comparison to other cell types they can be grown in larger amounts, are stable for many generations and are not affected by prior medication status of the patient .
The transport of both tyrosine and tryptophan has recently been characterized in fibroblast cells. Tyrosine was found mainly to be transported by system L, with LAT1 as the main transporter , in accordance with the transport of tyrosine through human brain microvascular endothelial cells [18, 20, 21]. Tyrosine is also, to a less extent, transported through system A, by its isoform ATA2 . System A is known to transport short-chain amino acids, such as alanine, but in a study by Vumma et al in 2008  it was demonstrated that approximately 50% of alanine was transported through the LAT1 isoform of system L, which denotes a competition between alanine and tyrosine to get transported. The transport of tryptophan in fibroblast cells is mediated by multiple transporters that are active at different substrate concentrations . However, at physiological tryptophan plasma concentrations the transport is mainly through the LAT1 isoform of system L .
When using the fibroblast cell model, previous findings by our group [23–29] and others  have shown a disturbed membrane transport of tyrosine in a number of psychiatric disorders, such as schizophrenia, autism and bipolar disorder, Moreover, in a previous study by our group, we found that children with autism had an increased transport capacity of alanine across cell membranes . An elevated transport of alanine across the BBB might influence the transport of other amino acids that are of vital importance for normal brain activity, since amino acids using the same transporter compete for transport [13, 15].
The aim of this study was to investigate whether children with ADHD have changes in the transport of tyrosine and/or tryptophan, since these amino acids are the precursors for the neurotransmitters implicated in the pathophysiology of ADHD. Moreover, as there is a competition between tyrosine and alanine we studied the transport of alanine in children with ADHD.
Materials and Methods
Children with ADHD
The study included fibroblast cell lines from 14 boys with ADHD of the combined type (inattention combined with hyperactivity and impulsivity), according to the DSM-IV criteria . They were between 6-12 years old (mean 10 years) at the time of the study. All were patients at the Unit of Neurodevelopmental Disorders, Department of Pediatrics, Skaraborg Hospital, Mariestad which is a primary pediatric referral center for pharmacological treatment of children and adolescents with ADHD. The patients had been diagnosed by an experienced team within the unit with support from standardized ADHD-rating scales used by clinicians, teachers and parents as well as with a general pediatric and psychological/cognitive work up. First grade relatives with ADHD or disruptive disorder, in addition to an uneventful pregnancy and perinatal period, were considered as an indication of heredity for ADHD. There were some true co-morbidities i.e., two boys had migraine and two other boys had asthma and still three others were overweight. Symptoms for motor coordination disorder, oppositional defiant disorder, conduct disorder, intellectual disability and autism spectrum disorder were checked for but not diagnosed at the time for the study. Both intellectual disability and autism spectrum disorder were exclusion criterias. All children were pharmacologically treated, twelve with methylphenidate and two with atomoxetine.
The comparison group consisted of fibroblast cell lines from 13 boys matched for age and without a diagnosis of a developmental disorder, between 7 and 13 years old (mean 10 years). Five of the 13 cell lines were used as controls in a previous study and were obtained from a Biobank . Eight skin biopsies were taken in connection with ear-nose and throat surgery (such as insertion of transmyringeal ventilation tubes).
Collection of biopsies
A 2 mm2 skin punch biopsy was taken after anaesthetizing the mid-forearm under aseptic conditions as described previously . The tissue was immediately placed in tubes containing complete culture medium and transported to the laboratory. From the biopsy was fibroblast cell lines cultured and stored in a Biobank (-196°C) until used for the experiments.
All growth media, antibiotics and fetal bovine serum (FBS) were obtained from Gibco Invitrogen cell culture (Sweden).
Tissue culture flasks and multi-well plates were from Costar Europe Ltd, Costar NY. 14C (U)-L-tyrosine with specific activity 486 mCi/mmol, 3H(5)-L-tryptophan with specific activity 30 Ci/mmol and 14C(U)-L- Alanine with specific activity 110 Ci/mmol were obtained from Larodan Fine Chemicals AB (Malmö, Sweden). D-Glucose was obtained from Ambresco (Ohio, USA) and phosphate buffered saline (PBS) was from the National Veterinary Institute (SVA) (Uppsala, Sweden). All other chemicals and amino acids were purchased from Sigma-Aldrich Sweden AB (Sweden). Scintillation cocktail (Optiphase, Hisafe 3) and liquid scintillation counter (Winspectral 1414) were from PerkinElmer Life Sciences (USA). Scintillation vials were purchased from Sarstedt AB (Sweden). Micro-well plates used for protein determination were purchased from Nunc (Roskilde, Denmark) and readings were done using Multiscan MS from Labsystems (Helsinki, Finland). All amino acid solutions were made in PBS and the pH was maintained between 7.35 and 7.40.
Fibroblast cells were cultured in plastic tissue culture flasks containing minimal essential medium (MEM) supplemented with 10% FBS, L-glutamine (2 mM/L), penicillin (100 mg/ml), streptomycin (100 mg/ml) and Amino-Max™. Cells were maintained in a humidified atmosphere of 5% CO2 in air at 37°C. Before the measurement of amino acid transport, cells were harvested when confluent and seeded in 2 cm2-multi-well plates and grown to confluence for approximately 5 days. Cell lines between 4th and 14th passages (number of splitting) were used in the experiments.
Transport assay of amino acids
Amino acid transport was measured using the cluster tray method for rapid measurement of amino acid flux in adherent fibroblast cells [25, 32, 33]. Fibroblasts grown in multi-well plates were washed twice with PBS and incubated with PBS containing 1% D-glucose for 1 hour at 37°C, to deplete the endogenous amino acid pools. After removal of the pre-incubation medium, the cells were incubated for 60 seconds at 37°C with a constant amount of 14C(U)- L-tyrosine or 3H(5)-L-tryptophan or 14C(U)-L-alanine and 12 different concentrations (varying between 0.004 and 1.5 mmol/L for tyrosine, 0.005 to 0.5 mmol/L for tryptophan and 0.02 to 6 mmol/L for alanine) of unlabelled amino acids. Amino acid transport was terminated by rapidly washing the cells twice with ice-cold PBS. The cells were then lysed in 0.2 ml of 0.5 mol/L sodium hydroxide (NaOH) for approximately 30 minutes. The radioactivity of the cell lysate was measured by liquid scintillation counting from a mixture of cell lysate and scintillation cocktail. The total amino acid uptake was correlated to the total amount of protein in each well, determined by the Bradford method , using bovine serum albumin as a standard.
The amino acid kinetic parameters V max and K m were calculated from the obtained uptake values, corrected for diffusion constant (K d ), by using the Lineweaver-Burke plot equation [1/V0 = (K m /V max [S] + (1/V max )] as described previously . V0 is the initial transport capacity, [S] is the substrate concentration, Vmax is the maximal transport capacity (nmol/min/mg protein) and Km, is the affinity constant (the concentration at half-saturation, μmol/L). Each experiment was performed in duplicate at the same time point for all amino acid transport assays and a mean value was taken for kinetic analysis.
All kinetic parameters are presented by descriptive statistics (mean with standard deviations or median with range). Assumptions about parametric methods were fulfilled for K m of tyrosine, tryptophan and alanine transport, but not for V max of tyrosine, tryptophan and alanine transport (determined using Shapiro-Wilk W test).
Significance of the difference in K m for tyrosine, tryptophan and alanine transport between children with ADHD and the comparison group was analysed using the Student's unpaired t-test. Significance of the difference in V max for tyrosine, tryptophan and alanine transport between children with ADHD and the comparison group was analysed using the Mann Whitney U test.
For all statistical analyses a significant level of 5% (two-tailed) was accepted. All statistical analyses were performed using PASW statistics version 18.0 for Windows.
The study was approved by the Regional Ethics Committee in Gothenburg, Sweden (Dnr: 218-07). A written and signed consent was obtained from the parent/s and their child before performing the studies.
Maximal transport capacity (V max ) and mean affinity of binding site (K m ) of tyrosine, tryptophan and alanine transport in children with ADHD and in controls are presented in Table 1.
There were no significant differences between the ADHD group and controls in any of the kinetic parameters regarding the tyrosine transport (V max ; p = 0.617, K m ; p = 0.645). The median V max for tyrosine transport was 15.1 (11.5-25.4) nmol/min/mg protein in the ADHD group and 15.5 (7.8-21.5) nmol/min/mg protein in the comparison group. The mean K m for tyrosine transport was 20.0 (6.3) μmol/L in the ADHD group and 18.8 (5.5) μmol/L in the comparison group.
The ADHD group had significantly decreased V max (p = 0.039) and K m (p = 0.010) for tryptophan transport in comparison to controls. The median V max for tryptophan transport in the ADHD group was 1.5 (1.1-3.0) nmol/min/mg protein and for the comparison group 2.0 (1.3-4.7) nmol/min/mg protein. The mean K m for tryptophan transport in the ADHD group was 13.6 (4.7) μmol/L and for the comparison group 21.1 (8.2) μmol/L.
They ADHD group had a significantly higher V max for alanine transport (p = 0.031) than the controls, but the Km for alanine transport did not differ significantly (p = 0.086). The median V max for alanine was 42.8 (36.3-64.9) nmol/min/mg protein in the group of children with ADHD, while the median V max for the comparison group was 32.0 (22.7-63.4) nmol/min/mg protein. The mean K m of alanine transport in the ADHD group was 125.7 (41.2) μmol/L and for the comparison group 100.7 (30.1) μmol/L.
The main finding in the present study was that the group with ADHD had a decreased V max of tryptophan transport and an elevated V max of alanine transport across the fibroblast cell membranes. A low V max implies that the transport systems have lower capacity for amino acid uptake, while an increased V max indicates the opposite. Hence, the children in the ADHD group had a decreased transport of tryptophan and an elevated transport of alanine through the cell membrane of fibroblasts. Several mechanisms could contribute to the differences found between the ADHD group and the controls; 1) altered expression of transporter proteins and/or mutation/s in the genes coding for the involved transporter proteins; 2) general changes in the cell membrane, such as a disturbed membrane phospholipid composition (MPC) that could be altering the structure of the transporter proteins embedded in the membrane, which in turn might change the functionality of the transporters; 3) the altered amino acid transport could be caused by some other molecule(s) affecting the transporter(s) indirectly, e.g. some cytokines are known to influence amino acid uptake [35–39].
The ADHD group also had a decreased K m for tryptophan transport, which corresponds to an increased affinity between the amino acid and the transport protein, indicating that a lower concentration of extracellular tryptophan is needed to reach maximal transport capacity. This could be a compensatory mechanism to the decreased V max . However, there was a negative correlation between the V max and K m values for tryptophan transport within the ADHD group (r = -0.70, p = 0.005).
The use of fibroblast cells as a human experimental model to study amino acid transport across the BBB has gained support by a number of previous studies [15, 23–29]. Moreover, the amino acid transport systems (i.e. system L and A) and their isoforms are expressed in both fibroblasts and at BBB [15, 40]. The present findings of altered amino acid transport in fibroblasts from children with ADHD might therefore also be present at the BBB.
Implications of an altered tryptophan transport
The decreased transport of tryptophan that was found in the ADHD group in the present study may imply reduced levels of serotonin in the CNS that might result in a disturbed serotonergic neurotransmission. A dysfunctional serotonergic system might secondarily lead to disturbances in the catecholaminergic systems as these neurotransmitter systems have strong anatomical and functional interactions .
Although the neurotransmitter most clearly implicated in ADHD is dopamine, there is a considerable amount of literature associating the serotonergic system with impulsivity, i.e. a core symptom in the combined type of ADHD . There are also evidences suggesting that serotonin may be important in the action of amphetamine to reduce impulsive behaviour, potentially via its interactions with the dopaminergic system . The dopamine-serotonin interaction and evidences for an altered dopaminergic and serotonergic contribution to ADHD were reviewed comprehensively by Oades . The author presented studies supporting the role of serotonergic activity in impulse responses and implications as potential target for pharmacotherapy. Moreover, adolescents with ADHD and disruptive behaviour were studied by Malmberg et al (2008) with respect to MAO-A and 5-HTT genes and platelet MAO-B activity. The importance of further investigations of the serotonergic system, in addition to the dopaminergic system, in individuals with ADHD and disruptive behaviour disorders was emphasized .
If the transport of tryptophan is decreased through the BBB, as our results indicate, increasing plasma concentration of tryptophan (e.g. via tryptophan supplementation) might not result in more serotonin production. This could be one reason for the inconsistent results for tryptophan supplementation approaches in the treatment of ADHD . However, some children with ADHD not responding to single treatment of psychostimulants are given a combination with selective serotonin reuptake inhibitors (SSRI) and show beneficial response.
Implications of an altered alanine transport
The physiological relevance of the increased alanine transport that was found in the ADHD group has not been explored. However, at physiological plasma concentrations there is a competition between amino acids for transport across the BBB [13–15]. Although alanine is not involved in the synthesis of neurotransmitters, an elevated transport of alanine might influence the transport of other amino acids that are of essential importance for normal brain activity. Moreover, since alanine is involved in many complex and important metabolic pathways [46, 47], our experiments cannot exclude that the elevated alanine transport might be related to other metabolic mechanisms of vital importance for normal brain activity. An increased transport of alanine has also been found in children with autism. ADHD and autism have high co-morbidity [48, 49], and the present finding might imply a shared amino acid transport disturbance.
Implications of an unaltered tyrosine transport
We did not find any significant differences in the transport of tyrosine between the ADHD group and the control group. Since tyrosine and tryptophan are considered to be transported across the BBB in similar fashion (i.e. through the LAT1 isoform of system L) it is difficult to explain why the tyrosine transport was not altered, whilst the tryptophan transport was. However, this indicates that it is not the overall capacity (expression) of system L that is affected; rather the isolated decrease in the V max for tryptophan could be linked to a more general alteration in plasma membrane function in ADHD. Altered membrane composition has been implicated in other psychiatric disorders such as schizophrenia and bipolar disorder [50–53]. Moreover, we measured the total transport of respective amino acids, i.e. we did not differentiate between the different transport systems and their isoforms.
Possible transporters involved in the altered amino acid transport found in the ADHD group
In fibroblasts the tryptophan transport is through different amino acid transport systems at different substrate concentrations . In this study we measured the transport of tryptophan at low concentrations (5 μM-500 μM of tryptophan), i.e. at physiological plasma concentrations of tryptophan (approximately 50 μM, physiological plasma levels of tyrosine and alanine are approximately 84 and 250 μM respectively). At this concentration, tryptophan is being transported through the LAT1 isoform of system L (approximately 80%) and through a high affinity system, which could be a hitherto undefined transporter or a variant of a known transport system with different functional properties due to an altered structure or conformation of the transporter protein. For example, system L is known to alter the transport properties due to different light-chain subunits [54, 55]. The present results could thus imply that it might be the undefined tryptophan transporter that is malfunctioning in ADHD and not the LAT1 transporter, since the tyrosine transport was not altered. If this undefined transporter of tryptophan also exists at the BBB is not known to date. However, tyrosine is also transported through the ATA2 isoform of system A, which is the major transporter of alanine. The alanine transport was increased in the ADHD group, indicated by an increased V max but unchanged K m , and this transport disturbance could be caused by different mechanisms (see above), such as a higher expression of the ATA2 transporter protein in the fibroblasts from children with ADHD. Hence, if the LAT1 transporter is disturbed, tyrosine could compulsorily be transported through the ATA2 transporter and therefore the V max of tyrosine transport will not be affected in the ADHD group.
There are certain limitations with the present study. The patient group was relatively small, i.e. fourteen children with ADHD. The plasma levels of amino acids were not determined at the time of the biopsy collection. A further limitation is that only boys were included. However, our intention was to include children with a very similar phenotype of ADHD according to gender, age, type of ADHD and etiology. To achieve this we selected only boys (with the combined type of ADHD) in a rather narrow age span and for almost all boys there were close relatives/family members with the same disorder. Moreover, the patients were on different medications at the time of the biopsy collection, but it seems rather unlikely that this would affect the results as the cultivated fibroblasts were seeded for multiple generations in vitro before being used in the experiments .
In conclusion, children with ADHD may have a decreased access of tryptophan and an elevated access of alanine in the brain. The decreased tryptophan availability in the brain might cause disturbances in the serotonergic neurotransmitter system, which secondarily might lead to changes in the catecholaminergic system. The physiological relevance of an increased access of alanine in the CNS has not been explored. However, this study was made in vitro, which makes it rather difficult to translate the results into in vivo situations. A further and extended exploration concerning the disturbance of amino acid transport in children with ADHD is thus necessary. Such exploration should include molecular investigations, looking for polymorphism in gene loci, further transport studies including girls with ADHD, measure the amount of serotonergic receptors in fibroblasts and study the effects of different molecules, such as cytokines, on amino acid uptake.
Biederman J, Faraone SV: Attention-deficit hyperactivity disorder. Lancet. 2005, 366: 237-248. 10.1016/S0140-6736(05)66915-2.
Polanczyk G, de Lima MS, Horta BL, Biederman J, Rohde LA: The worldwide prevalence of ADHD: a systematic review and metaregression analysis. Am J Psychiatry. 2007, 164: 942-948. 10.1176/appi.ajp.164.6.942.
Rader R, McCauley L, Callen EC: Current strategies in the diagnosis and treatment of childhood attention-deficit/hyperactivity disorder. American family physician. 2009, 79: 657-665.
Barkley RA, Brown TE: Unrecognized attention-deficit/hyperactivity disorder in adults presenting with other psychiatric disorders. CNS spectrums. 2008, 13: 977-984.
Thapar A, Langley K, Owen MJ, O'Donovan MC: Advances in genetic findings on attention deficit hyperactivity disorder. Psychological medicine. 2007, 37: 1681-1692.
Faraone SV, Perlis RH, Doyle AE, Smoller JW, Goralnick JJ, Holmgren MA, Sklar P: Molecular genetics of attention-deficit/hyperactivity disorder. Biological psychiatry. 2005, 57: 1313-1323. 10.1016/j.biopsych.2004.11.024.
Williams NM, Zaharieva I, Martin A, Langley K, Mantripragada K, Fossdal R, Stefansson H, Stefansson K, Magnusson P, Gudmundsson OO: Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet. 2010, 376: 1401-1408. 10.1016/S0140-6736(10)61109-9.
Prince J: Catecholamine dysfunction in attention-deficit/hyperactivity disorder: an update. Journal of clinical psychopharmacology. 2008, 28: S39-45. 10.1097/JCP.0b013e318174f92a.
Oades RD: Dopamine-serotonin interactions in attention-deficit hyperactivity disorder (ADHD). Prog Brain Res. 2008, 172: 543-565.
Seo D, Patrick CJ, Kennealy PJ: Role of Serotonin and Dopamine System Interactions in the Neurobiology of Impulsive Aggression and its Comorbidity with other Clinical Disorders. Aggress Violent Behav. 2008, 13: 383-395. 10.1016/j.avb.2008.06.003.
Fernstrom JD: Role of precursor availability in control of monoamine biosynthesis in brain. Physiol Rev. 1983, 63: 484-546.
Hyde R, Taylor PM, Hundal HS: Amino acid transporters: roles in amino acid sensing and signalling in animal cells. Biochem J. 2003, 373: 1-18. 10.1042/BJ20030405.
Pardridge WM: Blood-brain barrier carrier-mediated transport and brain metabolism of amino acids. Neurochem Res. 1998, 23: 635-644. 10.1023/A:1022482604276.
Pardridge WM, Oldendorf WH: Transport of metabolic substrates through the blood-brain barrier. J Neurochem. 1977, 28: 5-12. 10.1111/j.1471-4159.1977.tb07702.x.
Vumma R, Wiesel FA, Flyckt L, Bjerkenstedt L, Venizelos N: Functional characterization of tyrosine transport in fibroblast cells from healthy controls. Neurosci Lett. 2008, 434: 56-60. 10.1016/j.neulet.2008.01.028.
Mahadik SP, Mukherjee S: Cultured skin fibroblasts as a cell model for investigating schizophrenia. J Psychiatr Res. 1996, 30: 421-439. 10.1016/S0022-3956(96)00025-8.
Stahl SM: Peripheral models for the study of neurotransmitter receptors in man. Psychopharmacol Bull. 1985, 21: 663-671.
Umeki N, Fukasawa Y, Ohtsuki S, Hori S, Watanabe Y, Kohno Y, Terasaki T: mRNA expression and amino acid transport characteristics of cultured human brain microvascular endothelial cells (hBME). Drug Metab Pharmacokinet. 2002, 17: 367-373. 10.2133/dmpk.17.367.
Vierbuchen T, Ostermeier A, Pang ZP, Kokubu Y, Sudhof TC, Wernig M: Direct conversion of fibroblasts to functional neurons by defined factors. Nature. 2010, 463: 1035-1041. 10.1038/nature08797.
Choi TB, Pardridge WM: Phenylalanine transport at the human blood-brain barrier. Studies with isolated human brain capillaries. J Biol Chem. 1986, 261: 6536-6541.
Hawkins RA, O'Kane RL, Simpson IA, Vina JR: Structure of the blood-brain barrier and its role in the transport of amino acids. J Nutr. 2006, 136: 218S-226S.
Ravi V, Jessica J, Tommy L, Nikolaos V: Tryptophan Transport in Human Fibroblast Cells - A Functional Characterization. International Journal of Tryptophan Research. 2011, 4: 19-27. http://www.la-press.com/tryptophan-transport-in-human-fibroblast-cells-a-functional-characteri-article-a2600
Bjerkenstedt L, Farde L, Terenius L, Edman G, Venizelos N, Wiesel FA: Support for limited brain availability of tyrosine in patients with schizophrenia. Int J Neuropsychopharmacol. 2006, 9: 247-255.
Fernell E, Karagiannakis A, Edman G, Bjerkenstedt L, Wiesel FA, Venizelos N: Aberrant amino acid transport in fibroblasts from children with autism. Neurosci Lett. 2007, 418: 82-86. 10.1016/j.neulet.2007.03.004.
Flyckt L, Venizelos N, Edman G, Bjerkenstedt L, Hagenfeldt L, Wiesel FA: Aberrant tyrosine transport across the cell membrane in patients with schizophrenia. Arch Gen Psychiatry. 2001, 58: 953-958. 10.1001/archpsyc.58.10.953.
Olsson E, Wiesel FA, Bjerkenstedt L, Venizelos N: Tyrosine transport in fibroblasts from healthy volunteers and patients with schizophrenia. Neurosci Lett. 2006, 393: 211-215. 10.1016/j.neulet.2005.09.070.
Wiesel FA, Andersson JL, Westerberg G, Wieselgren IM, Bjerkenstedt L, Hagenfeldt L, Langstrom B: Tyrosine transport is regulated differently in patients with schizophrenia. Schizophr Res. 1999, 40: 37-42. 10.1016/S0920-9964(99)00029-8.
Wiesel FA, Venizelos N, Bjerkenstedt L, Hagenfeldt L: Tyrosine transport in schizophrenia. Schizophr Res. 1994, 13: 255-258. 10.1016/0920-9964(94)90050-7.
Persson ML, Johansson J, Vumma R, Raita J, Bjerkenstedt L, Wiesel FA, Venizelos N: Aberrant amino acid transport in fibroblasts from patients with bipolar disorder. Neurosci Lett. 2009, 457: 49-52. 10.1016/j.neulet.2009.03.095.
Ramchand CN, Peet M, Clark AE, Gliddon AE, Hemmings GP: Decreased tyrosine transport in fibroblasts from schizophrenics: implications for membrane pathology. Prostaglandins Leukot Essent Fatty Acids. 1996, 55: 59-64. 10.1016/S0952-3278(96)90146-5.
American Psychiatric Association, Diagnostics and Statistical Manual of Mental Disorders (DSM-IV). 1994, Washington DC: American Psychiatric Press, 4
Gazzola GC, Dall'Asta V, Franchi-Gazzola R, White MF: The cluster-tray method for rapid measurement of solute fluxes in adherent cultured cells. Anal Biochem. 1981, 115: 368-374. 10.1016/0003-2697(81)90019-1.
Hagenfeldt L, Venizelos N, Bjerkenstedt L, Wiesel FA: Decreased tyrosine transport in fibroblasts from schizophrenic patients. Life Sci. 1987, 41: 2749-2757. 10.1016/0024-3205(87)90468-1.
Bradford MM: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976, 72: 248-254. 10.1016/0003-2697(76)90527-3.
Feneant-Thibault M, Galera P, Maccario J, Boutron A, Pujol JP, Moatti N: Interleukin-1 beta-induced changes in the kinetic constants of L-proline uptake in human skin fibroblasts. Biochem J. 1991, 276 (Pt 1): 57-62.
Goenner S, Cosson C, Boutron A, Legrand A, Moatti N: Interleukin-1 beta and interleukin-6 stimulate 2-methylaminoisobutyric acid uptake in HepG2 cells. Int J Biochem Cell Biol. 1997, 29: 667-674. 10.1016/S1357-2725(97)00002-2.
Le Maire V, Solito E, Russo-Marie F, Hernvann A, Le Marechal H, Ekindjian OG, Aussel C: System A neutral amino acid transporter regulation by interleukin-1beta in human osteoarthritic synovial cells: evidence for involvement of prostaglandin E(2) as a second messenger. J Cell Physiol. 2000, 183: 65-73. 10.1002/(SICI)1097-4652(200004)183:1<65::AID-JCP8>3.0.CO;2-H.
Subramanian M, Kuang PP, Wei L, Rishikof DC, Liu H, Goldstein RH: Modulation of amino acid uptake by TGF-beta in lung myofibroblasts. J Cell Biochem. 2006, 99: 71-78. 10.1002/jcb.20849.
Thongsong B, Subramanian RK, Ganapathy V, Prasad PD: Inhibition of amino acid transport system a by interleukin-1beta in trophoblasts. J Soc Gynecol Investig. 2005, 12: 495-503. 10.1016/j.jsgi.2005.06.008.
Prasad PD, Wang H, Huang W, Kekuda R, Rajan DP, Leibach FH, Ganapathy V: Human LAT1, a subunit of system L amino acid transporter: molecular cloning and transport function. Biochem Biophys Res Commun. 1999, 255: 283-288. 10.1006/bbrc.1999.0206.
Kapur S, Remington G: Serotonin-dopamine interaction and its relevance to schizophrenia. Am J Psychiatry. 1996, 153: 466-476.
Oades RD: Role of the serotonin system in ADHD: treatment implications. Expert Rev Neurother. 2007, 7: 1357-1374. 10.1586/14737220.127.116.117.
Winstanley CA, Eagle DM, Robbins TW: Behavioral models of impulsivity in relation to ADHD: translation between clinical and preclinical studies. Clin Psychol Rev. 2006, 26: 379-395. 10.1016/j.cpr.2006.01.001.
Malmberg K, Wargelius HL, Lichtenstein P, Oreland L, Larsson JO: ADHD and Disruptive Behavior scores-associations with MAO-A and 5-HTT genes and with platelet MAO-B activity in adolescents. BMC Psychiatry. 2008, 8: 28-10.1186/1471-244X-8-28.
Arnold LE: Treatment alternatives for Attention-Deficit! Hyperactivity Disorder (ADHD). Journal of Attention Disorders. 1999, 3: 30-48. 10.1177/108705479900300103.
Felig P: Amino acid metabolism in man. Annu Rev Biochem. 1975, 44: 933-955. 10.1146/annurev.bi.44.070175.004441.
Yudkoff M, Nissim I, Daikhin Y, Lin ZP, Nelson D, Pleasure D, Erecinska M: Brain glutamate metabolism: neuronal-astroglial relationships. Dev Neurosci. 1993, 15: 343-350. 10.1159/000111354.
Cormier E: Attention deficit/hyperactivity disorder: a review and update. Journal of pediatric nursing. 2008, 23: 345-357. 10.1016/j.pedn.2008.01.003.
Gillberg C, Gillberg IC, Rasmussen P, Kadesjo B, Soderstrom H, Rastam M, Johnson M, Rothenberger A, Niklasson L: Co-existing disorders in ADHD -- implications for diagnosis and intervention. European child & adolescent psychiatry. 2004, 13 (Suppl 1): I80-92.
Dubovsky SL, Murphy J, Christiano J, Lee C: The calcium second messenger system in bipolar disorders: data supporting new research directions. J Neuropsychiatry Clin Neurosci. 1992, 4: 3-14.
Ehrlich BE, Diamond JM: Lithium, membranes, and manic-depressive illness. J Membr Biol. 1980, 52: 187-200. 10.1007/BF01869189.
Lachman HM, Papolos DF: Abnormal signal transduction: a hypothetical model for bipolar affective disorder. Life Sci. 1989, 45: 1413-1426. 10.1016/0024-3205(89)90031-3.
Horrobin DF: The membrane phospholipid hypothesis as a biochemical basis for the neurodevelopmental concept of schizophrenia. Schizophr Res. 1998, 30: 193-208. 10.1016/S0920-9964(97)00151-5.
Seymour RL, Ganapathy V, Mellor AL, Munn DH: A high-affinity, tryptophan-selective amino acid transport system in human macrophages. J Leukoc Biol. 2006, 80: 1320-1327. 10.1189/jlb.1205727.
Verrey F: System L: heteromeric exchangers of large, neutral amino acids involved in directional transport. Pflugers Arch. 2003, 445: 529-533.
The authors are indebted to professor Mats Bende and research assistant Christel Larsson for important help with the collection of biopsies from the controls. We also thank the pediatric nurse at the Unit of Developmental Disorders, Skaraborgs hospital, Carina Höglund, for valuable collaboration. The study was supported by grants from the Research and Development Center Skaraborg Hospital ( FoU center) and the Faculty of Health and Medicine, Örebro University, Sweden.
The authors declare that they have no competing interests.
JJ, carried out 70% of primary cultures from skin biopsy specimens, all tryptophan and alanine transport experiments, literature searches, statistical analysis and wrote the first draft of the manuscript. ML, participated in the design of the study and in the recruitment of the patients. EF, participated in the design, coordinated the recruitment of the patients and controls and contributed to the manuscript writing. RV, carried out 30% of primary cultures from skin biopsy specimens, and all tyrosine transport studies. AÅ, participated in the design of the study. LB, participated in the design of the study. NV, conceived, participated in the design, took the biopsies, interpreted the findings and coordinated the whole study. All authors have contributed to and approved the final manuscript.
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Johansson, J., Landgren, M., Fernell, E. et al. Altered tryptophan and alanine transport in fibroblasts from boys with attention-deficit/hyperactivity disorder (ADHD): an in vitro study. Behav Brain Funct 7, 40 (2011). https://doi.org/10.1186/1744-9081-7-40
- Autism Spectrum Disorder
- Amino Acid Transport
- ADHD Group
- Amino Acid Uptake