Molecular Image-Guided Theranostic and Personalized Medicine 2012View this Special Issue
Research Article | Open Access
Reduced Striatal Dopamine Transporters in People with Internet Addiction Disorder
In recent years, internet addiction disorder (IAD) has become more prevalent worldwide and the recognition of its devastating impact on the users and society has rapidly increased. However, the neurobiological mechanism of IAD has not bee fully expressed. The present study was designed to determine if the striatal dopamine transporter (DAT) levels measured by -TRODAT-1 single photon emission computed tomography (SPECT) brain scans were altered in individuals with IAD. SPECT brain scans were acquired on 5 male IAD subjects and 9 healthy age-matched controls. The volume (V) and weight (W) of bilateral corpus striatum as well as the -TRODAT-1 uptake ratio of corpus striatum/the whole brain (Ra) were calculated using mathematical models. It was displayed that DAT expression level of striatum was significantly decreased and the V, W, and Ra were greatly reduced in the individuals with IAD compared to controls. Taken together, these results suggest that IAD may cause serious damages to the brain and the neuroimaging findings further illustrate IAD is associated with dysfunctions in the dopaminergic brain systems. Our findings also support the claim that IAD may share similar neurobiological abnormalities with other addictive disorders.
The use of the internet has expanded incredibly across the world over the last few years. The internet provides remote access to others and abundant information in all areas of interest. However, maladaptive use of the internet has resulted in impairment of the individual’s psychological well-being, academic failure, and reduced work performance and, especially leaded to internet addiction disorder (IAD) [1–4]. IAD was first raised in 1990s  and according to the Beard’s definition of IAD, “an individual is addicted when an individual’s psychological state, which includes both mental and emotional states, as well as their scholastic, occupational, and social interactions, is impaired by the overuse of the medium.” 
In recent years, IAD has become more prevalent worldwide; the recognition of its devastating impact on the users and society has rapidly increased . Importantly, recent studies have found dysfunctions of IAD are similar to other types of addictive disorders, such as substance abuse disorders and pathological gambling [7–10]. People experiencing IAD showed clinical features such as craving, withdrawal and tolerance [7, 8], increased impulsiveness , and impaired cognitive performance in tasks involving risky decision-making .
As similar with the abnormalities in the dopaminergic neural system in individuals with substance-related addiction , the role of dopaminergic neural system in IAD also has been elucidated in a few researches [12–14]. In a recent study, people with IAD were found to have altered resting-state glucose metabolism in several brain regions including the major dopamine projection areas such as the striatum and orbitofrontal region . Moreover, another study found that adolescents with increased genetic polymorphisms in genes coding for the dopamine D2 receptor and dopamine degradation enzyme were more susceptible to excessive internet gaming compared with an age-matched cohort of controls . In a positron emission tomography (PET) imaging study, reduced levels of dopamine D2 receptor in subdivisions of the striatum including the bilateral dorsal caudate and right putamen were found in the individuals with IAD . Taken together, these findings suggest that IAD may also be partly due to impaired dopaminergic neural systems similar to substance-related addiction .
Dopamine transporter (DAT) is a protein situated in the presynaptic terminal and striatal DAT is responsible for the active dopamine reuptake into the presynaptic neuron and plays a critical role in the regulation of striatal synaptic dopamine levels [16–18]. Altered DAT concentration in the striatum following chronic substance administration has been reported previously [19–24]. However, whether the abnormality of DAT also exists in IAD has not been illustrated before.
In recent years, imaging of DAT has been used as an important tool in clinical settings to display changes in the brain structure of patients with substance-related addiction [21–24]. In addition, the radiotracer 99mTc-TRODAT-1, a technetium-99 m (99mTc) labeled tropane derivative (technetium,2-[[2-[[[[3-(4-chlorophenyl)-8-methyl-8-azabicyclo oct-2-yl]-methyl](2-mercaptoethyl)amino]ethyl]amino]ethanethiolato(3-)]-oxo-[1R-(exo-exo)]-), is regarded as a safe and suitable imaging agent for monitoring DAT status for human imaging studies [21, 25, 26]. In the present study, we used single photon emission tomography (SPECT) with the radiotracer 99mTc-TRODAT-1 to investigate striatal DAT density to identify potential presynaptic abnormalities in IAD subjects compared to age-matched healthy controls. This study aims to test the hypothesis that the altered availability of DAT is associated with the pathogenesis of IAD.
2. Materials and Methods
2.1. Diagnosed Criteria of IAD
IAD was assessed using Young’s Internet Addiction Diagnostic Questionnaire (IADDQ)  and Goldberg’s Internet addictive Disorder Diagnostic Criteria (IADDC) . All of the questions of IADDQ and IADDC were translated into Chinese. To be eligible, participants in the IAD group were asserted that five or more “yes” responses to the eight questions of IADDQ and to satisfy three or more of IADDC (i.e., tolerance, withdrawal, craving and unplanned use, failure to reduce use, excessive use, sacrificing social activities to use, and physical and psychological problems associated with use).
Five men (mean ± SD, years old) with IAD were randomly selected from the patients seeking treatment at the Peking University Shenzhen Hospital. The IAD subjects used the internet almost everyday, and spend more than 8 hours (mean ± SD, hours) everyday in front of the monitor, mostly for chatting with cyber friends, playing online games, and watching online pornographies or adult movies. These subjects were initially familiar with internet mostly at the early stage of their adolescence (mean age ± SD, years old) and had the indications of IAD for more than 6 years (, years).
Nine age-matched controls (, years old) recruited through advertisement participated in this study. No statistical difference was found for the ages of the participants between the two groups (). The participants in the control group used Internet occasionally or frequently but spent no more than 5 hours a day on the line (mean ± SD, hours) and did not satisfy the diagnosed criteria of IAD [4, 27].
All the recruited participants were native Chinese speakers, never used illegal substances (sometimes, a few of the participants smoked or drink alcohol, but none of them meet the diagnosis criteria of substance-related disorders ), had no history of significant medical, neurological or psychiatric diseases, and were right-handed. All the participants gave written informed consent before participation after the nature of the procedure was fully explained, including possible risks and side effects. All procedures for this study were approved by the ethics committee of the Peking University Shenzhen Hospital.
TRODAT-1 ligand (liquid) was supplied by the Department of Chemistry, Beijing Normal University (Beijing, China). The radiotracer 99mTc-TRODAT-1, 740 MBq (20 mCi) with purity >90% was synthesized as described previously . And SPECT studies with 99mTc-TRODAT-1 were carried out using a Siemens DIACAM/E.CAM/ICON double detector SPECT with lower-energy all-purpose collimator (Siemens, Erlangen, Germany). The imaging method was performed as described previously [25, 29]. Subjects were injected intravenously with 740 MBq (20 mCi) of 99mTc-TRODAT-1. Imaging was performed 2.5 h after the administration of 99mTc-TRODAT-1. The acquisition parameters included 64 views over 18 s per view and a matrix over 360° with a rotation in 5.6° increments. Transverse reconstruction backprojection was applied to the raw data. A Butterworth filter was then applied with an order of 15 and a cutoff of 0.33 Nyquist frequency. Photon attenuation correction was performed using Chang’s first order correction method using an attenuation coefficient of 0.15 cm−1 . The transverse image thickness was 2.7 mm (1 pixel). All images were processed and reconstructed using the same procedure.
2.4. Image Analysis
Image analysis was done using the region ratio software of the E-Cam. Regions of interest (ROIs) were drawn on 12 transverse images, the pixels were extracted and counts of whole brain and bilateral corpus striatum were carried out. The volume (V) and weight (W) of bilateral corpus striatum as well as the ratio of corpus striatum/the whole brain (Ra) was calculated using the mathematical models as described in the previous paper [21, 31].
2.5. Data Analysis
Data in the present paper are presented as means ± standard (mean ± SD). Statistical Program for the Social Sciences for Windows, version 11 (SPSS 13.0, SPSS Inc, Chicago, USA) was used to analyze the data. Differences between the groups were assessed by Student’s t-test. For all of the tests conducted, the criterion for significance was set at .
The DAT images of the bilateral corpus striatum in the control group showed a panda-eye shape and DATs were distributed uniformly and symmetrically in the corpus striatum. The bilateral corpus striatum was situated on 8–12 layers, as shown in Figure 1(b). However, the DAT images of the IAD subjects displayed different levels of abnormity, in which the corpus stratums were much smaller and showed different shapes, dumbbell, thin strip, lunate shape, or sporadic spot (Figure 1(a)).
As shown in Figure 1 and Table 1, DAT expression level of striatum was significantly decreased in IAD subjects. Briefly, in comparison with the controls, there were significantly lower values of V (cm3), W (g) and Ra of corpus striatum in the IAD group, suggesting that decreased 99mTc-TRODAT-1 bound to DAT or impairment as well as dysfunction of corpus striatum occurred. No statistical difference was found as comparing V or W of the bilateral corpus striatum (left side and right side) either in the IAD group ( and resp.) or in the health control group ( and resp.).
|Values are expressed as mean ± SD with and .|
IAD resulted in impaired individual psychological well-being, academic failure, and reduced work performance, especially among adolescents [1–4]. However, there is currently no standardized treatment targeted for IAD. To develop effective methods for intervention and treatment of IAD, it will first require establishing a clear understanding of the underlying neurobiological mechanisms. In the present study, we assessed the DAT expression level in IAD subjects and healthy controls using 99mTc-TRODAT-1 SPECT. We found that DAT expression level of striatum was significantly decreased and the values of V, W, and Ra of the corpus striatum in IAD subjects were greatly reduced. The imaging results provided the direct-viewing proof of altered availability of DAT in brain of people with IAD.
DATs play a critical role in the regulation of striatal synaptic dopamine levels [16–18] and have been used as markers of the dopamine terminals . A reduced number of cell membrane DATs may possibly reflect pronounced striatal dopamine terminal loss or the brain dopaminergic function impairment which has been found in substance-related addiction [21–23]. PET imaging studies have found increased release of dopamine in the striatum during the video game . Patients with pathological gambling also demonstrated high level of dopamine in the ventral striatum during gambling . Because increased extracellular dopamine in the striatum is associated with subjective descriptors of reward (high, euphoria) [11, 35], individuals with IAD may also experience euphoria as the extracellular dopamine in the striatum increases. However, long-time and high concentrations of dopamine have been shown to cause a selective lesion of dopamine terminals [32, 36] and decreased size of dopaminergic cell bodies . Taken together, the reduced DATs found in our study may indicate the neuropathologic damage to the dopaminergic neural system caused by IAD.
According to our knowledge, this is the first imaging study to examine the abnormality of DAT in the brain of IAD subjects. Furthermore, the imaging results of the present study provide the objective proofs that long-term maladaptive use internet might cause serious problems. However, for complete interpretation of the results of the present study, some limitations should be noted. Firstly, the small sample size of our study may limit the generalizability of our results. Those positive associations in our study might have been due to chance or a stratification effect in the sample collection, and further studies in independent samples or a larger population are required. Secondly, the IAD subjects in the present study reported different desired activities when they are sitting in front of the monitor (including chatting with cyber friends, playing online games, watching online pornographies or adult movies, etc.). Our study can not determine whether the different types of Internet behaviors may cause different brain DAT changes. Therefore, the present study can only be recognized as exploratory and primary, and more research work should be done before we get the most definitive conclusion.
The results from this study provide evidence that IAD may induce significant DAT losses in the brain and these findings suggest that IAD is associated with dysfunctions in the dopaminergic brain systems and are consistent with previous reports in various types of addictions either with or without substances [21–23, 37]. Our findings support the claim that IAD may share similar neurobiological abnormalities with other addictive disorders .
H. Hou and S. Jia are contributed equally to this work.
This work is partly sponsored by Grants from the Zhejiang Provincial Natural Science Foundation of China (Z2110230), Health Bureau of Zhejiang Province (2010ZA075, 2011ZDA013), National Science Foundation of China (NSFC) (no. 81101023, 81170306, 81173468), and Ministry of Science and Technology of China (2011CB504400, 2012BAI13B06).
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