Research Article | Open Access
Chinese Medicine Formula “Jian-Pi-Zhi-Dong Decoction” Attenuates Tourette Syndrome via Downregulating the Expression of Dopamine Transporter in Mice
Jian-Pi-Zhi-Dong Decoction (JPZDD) is dedicated to the treatment for Tourette syndrome (TS) with the guidance of the theories of Traditional Chinese Medicine (TCM). This study aims to investigate the expression of dopamine transporter (DAT) in the striatum and stereotyped behavior of TS mice model by intervention of JPZDD. Mice were induced by 3,3′-iminodipropionitrile (IDPN, 350 mg kg−1 day−1, i.p.) for 7 days and divided into 4 groups (, each): control and IDPN groups were gavaged with saline and the remaining 2 groups with Tiapride (Tia, 50 mg kg−1 day−1) and JPZDD (20 g kg−1 day−1), respectively. The results showed that the scores of stereotyped behavior in IDPN+JPZDD group were significantly reduced. A noticeably increased 11C-β-CFT binding at bilateral striatum was observed after administration of JPZDD versus that of IDPN or Tia. Immunohistochemistry and in situ hybridization studies manifested higher levels of DAT protein and mRNA in IDPN+JPZDD group. These findings not only demonstrated that JPZDD could effectively inhibit the abnormal behaviors of TS mice model, but also increase the level of DAT in striatum. Therefore, JPZDD could be one of potential treatments of patients with TS.
Tourette syndrome (TS) is a chronic neurobehavioral disorder characterized by involuntary motor and phonic tics. TS usually starts at childhood with peak age from 7 to 15 years and persists to late adolescence or even early adulthood. Tics are more common in males than in females with the ratio of 3–9 : 1 . The morbidity in children is about 1% while only 0.3%–0.5% in adults. 35%–50% TS children could trace back to their affected first-degree relatives [2, 3]. In addition, TS patients often accompanied with attention deficit hyperactivity disorder (ADHD) and obsessive compulsive disorder (OCD).
Abnormal dopaminergic activity in the synaptic cleft has been considered as an important factor in TS for a long time. This hypothesis is supported by several evidences such as excessive dopaminergic activity in the nigrostriatum of basal ganglia circuit, releasing of surplus DA during tonic phase and the beneficial effect of tentative medication of DA precursor levodopa (L-DOPA) or DA antagonists on clinic symptoms . Dopamine transporter (DAT), a glycoprotein localized exclusively at presynaptic membrane of DA neurons, is responsible for modulating the concentration of extrasynaptic DA by reuptaking it into neurons and therefore plays an important role in keeping the phasic-tonic balance of DA releasing. A Functional neuroimaging study suggested that reduced activity of DAT in regulation of tonic DA releasing might underlie subsequent pathological states in TS .
It has been documented that psychomotor stimulant drugs like amphetamine and cocaine may be the causes of tics from clinical pharmacology. Moreover, methamphetamine at different doses could increase locomotor activity or elicit stereotypic behavior in rats [6, 7]. These excitatory substances act as substrates to block DAT-mediated uptake of DA or reversely promote DAT-mediated DA efflux .
Previous clinical study has proven that Jian-Pi-Zhi-Dong Decoction (JPZDD) was an effective antitics agent with overall response rate of reducing tics at 86.8% . The present study aimed to evaluate the anti-tics function of JPZDD from an animal model, and explored tentatively if abnormal expression of DAT existing in TS has relevance to severity of stereotyped behavior.
2. Materials and Methods
2.1. Drugs and Reagents
3,3′-iminodipropionitrile (IDPN) was purchase from Sigma-Aldrich Co. LLC. (USA), Tiapride (Tia) from Jiangsu Nhwa Pharmaceutical Co. Ltd. (Jiangsu, China), rat anti-N-terminal of DAT monoclonal antibody (primary antibody, 1 : 1000) from Millipore Co. (Billerica, MA, USA), goat-anti-rat IgG (H+L) antibody (secondary antibody, 1 : 250) and rabbit ABC detection 1/4 kit from Vector Labs, Inc. (Burlingame, CA, USA), DAT mRNA in situ hybridization kit from Wuhan Boster Oio-Engineering Co. Ltd. (Wuhan, China), and 11C-β-CFT was synthesized and provided from Department of Nuclear Medicine, Chinese PLA General Hospital (Beijing, China).
2.2. Preparation of JPZDD
The JPZDD formula includes 10 different Chinese medicinal herbs (Table 1). They were purchased from pharmaceutical department of Dongfang Hospital affiliated to Beijing University of Chinese Medicine (BUCM). Director Qing-chun Hao identified components, and the voucher specimens were deposited. All of them were soaked for 1 h at room temperature and decocted with distilled water for 2 h. The filtrates were condensed and dried by a vacuum-desiccator at 60°C. The extracted granules were analyzed by infrared fingerprint compared with standards to guarantee the qualified rate of more than 90% then packaged and stored at room temperature.
2.3. Experimental Animals and Behavior Recordings
Eighty ICR mice (male, aged 4 weeks, and g) were purchased from Vital River Laboratories (Beijing, China). All animal experimental protocols conformed to the Animal Management Rules of the Chinese Ministry of Health, and the study was approved by the animal ethics committee of the Chinese Academy of Medical Sciences. They were housed 10 per cage in an air-conditioned animal room with 12 h light/dark cycle, allowed access to water and food ad libitum, maintained in a constant temperature °C and humidity %, and fed for 1 w before generating TS model. After 1 w, mice were randomly divided into the saline group (control group) () and the TS model group (). The former were intraperitoneally injected (i.p.) with saline (0.9%) (15 mL kg−1); the later were injected with IDPN (350 mg kg−1, i.p.) once a day for 7 consecutive days. IDPN mice model groups were further divided into 3 groups: IDPN group (), IDPN+Tia group (), and IDPN+JPZDD group (). The ethological score between each group was balanced referring to the evaluating grade of stereotypy (Table 2) [10, 11]. The saline and IDPN groups were gavaged with saline (0.9%) at 20 mL kg−1, IDPN+Tia group with Tia at 50 mg kg−1, and IDPN+JPZDD group with JD at 20 g kg−1, respectively, once a day for 8 consecutive weeks. Behavioral recordings began once every 7 d after IPDN induction and drug administrations and were conducted by 2 trained observers, who were familiar to the measurements but blind to the group condition. Each animal was observed for 1 min of every 5 min for a total of 6 periods. One or more episodes which were in accordance with the grades got the corresponding score and calculated the average score on the basis of results from 2 observers, as the objective indicator of behavioral changes.
2.4. MicroPET Scans
Imaging study with 11C-β-CFT was conducted 1 d after the last behavior test of each mouse. 11C-β-CFT was synthesized from its corresponding precursors 11C-Triflate-CH3 and nor-β-CFT, with a radiochemical purity of more than 95% . Each mouse was injected with 1 mCi 11C-β-CFT through the caudal vein. After 20–25 min till the radiotracer was generalized uptake, each was anesthetized with 3.5% chloral hydrate through intraperitoneal injection and fixed in a self-made animal framework on which 2 mice lay head-to-head in a prone position. Each was scanned 15 min with its brain centered in the axial and transaxial fields of view (Explore VISTA Micro-PET/CT scanner from GE Healthcare Co., USA). Image data were sorted into 3D sinograms, followed by Fourier rebinning and 2D ordered subset expectation maximization reconstruction with 2 iterations and 50 subsets. The images pixel size was 0.385 × 0.385 0.385 mm. For semiquantitative evaluation, the regions of interest (ROI) (right/left striatum and cerebellum) were measured 3 times, and the ratio of striatum to cerebellum was counted with mean value of the measurements.
Expression of DAT protein was detected by immunohistochemistry one day after PET scan. Mice were perfused and fixed with 4% PFA after anesthetizing with 10% chloral hydrate. The global brains were stripped off and soaked in 4% PFA for 14 h. The fixed brains were dehydrated by 30% sucrose for 24 h and embedded in OCT medium after cryoprotection. Frozen brains were cut into 30 μm coronal sections prelocated at caudate putamen by a refrigerated microtome (Shandon, GB). Sections were immersed into 3% hydrogen peroxide solution to inactivate the endogenous peroxidase and blocked by 10% goat serum at room temperature, incubated by the primary antibody at 4°C overnight, then by the secondary antibody at room temperature for 2 h, finally by avidin-biotin-peroxidase complex for 90 min. Sections were visualized by DAB for 5 min then mounted by neutral balsam. 6 visual fields were chosen randomly from bilateral colored striatum under an upright microscope at 100x magnification. Quantifications were performed by Image-pro plus 6.0 analysis system to calculate the optical density (OD) of each field. The values of DAT protein were chosen and counted from every three brain slices of each mouse with similar forms.
2.6. In Situ Hybrization
Brain sections were deparaffinizated by mixed solution of 30% hydrogen dioxide and absolute methanol (1 : 50) for 30 min at room temperature. Several drops of diluted pepsin solution were added to slices for proteolysis and exposure of mRNA at 37°C for 2 min and fixed by 1% paraformaldehyde (PH = 7.2–7.6). Prehybridization was performed at 42°C for 4 h with prepared DAT mRNA in situ hybridization kit and hybridization at 42°C overnight in calorstat (SPX-150C, Boxun Industrial Co. Ltd., Shanghai, China). All sections were washed, blocked, incubated with streptavidin biotin-peroxidase complex (SABC) and biotin-peroxidase at 37°C for 30 min, and finally visualized with DAB for 30 min before alcoholic dehydration and mounting. The slices were observed and microphotographed under the light microscope. The values of OD reflecting the expression of DAT mRNA were determined by Metamorph image processing analysis system from Diagnostic Tool Electrics Co., USA.
2.7. Statistical Analysis
Results were expressed as the mean ± SEM. Statistical differences between groups were determined by one-way analysis of variance (ANOVA). Student-Newman-Keuls (SNK) test was employed for the comparison of parameters if the analysis of ANOVA had significant difference. All analyses were performed by the SPSS 18.0 (SPSS Inc., Chicago, IL, USA), and value < 0.05 was accepted as statistically significant.
3.1. Behavior Study
TS mouse model induced by IDPN showed abnormal stereotypes in different degrees. Remarkably, severity of stereotypes in either IDPN+Tia or IDPN+JPZDD group decreased significantly as compared to IDPN alone group (). Comparison between administrated groups showed the average score of JPZDD was lower than Tia () at the end of experiment, although it was still higher than that of saline group () (Figure 1).
3.2. MicroPET Imaging
Coronal scans manifested by PET imaging showed high tracer accumulation at bilateral striatum regions in saline group with uniform distribution and symmetric morphous. Marked fuzzy images and low accumulation of 11C-β-CFT were observed in TS mice model (Figure 2(a)). After 8 w, the uptake ratio of 11C-β-CFT was significantly higher in both Tia and JPZDD treated groups than that in IDPN group (). Furthermore, the uptake ratio of 11C-β-CFT in IDPN+JPZDD group was significantly better than that in IDPN+Tia group () (Figure 2(b)).
3.3. DAT Expressions in the Striatum
In order to further investigate the activity and quantity of DAT in the striatum under diverse medications, DAT protein and mRNA expression were assessed by immunohistochemistry and in situ hybrization. DAT protein was decreased in IDPN group compared with that in saline group () (Figures 3(a)-3(b)). Moreover, IDPN+JPZDD and IDPN+Tia, respectively, could prompt the abundance of DAT, and more notable improvement was observed in JPZDD treated mice (). The level of DAT mRNA (Figures 3(c)-3(d)) also revealed that IDPN alone dramatically reduced DAT mRNA abundance. However, treatments of JPZDD and Tia, respectively, increased DAT mRNA abundance by 18% and 41% as compared to that of IDPN group.
From the viewpoint of TCM, children with TS usually suffer from excessive energy of the liver and deficiency of the spleen. Based on this theory we hypothesized that imbalance of liver and spleen in TS patients generates endogenous liver wind and spleen phlegm, where liver wind agitates, and spleen phlegm obstructs the channels. According to this hypothesis, we created a recipe named as JPZDD that includes two ancient formulae of Liu-Jun-Zi-Tang (LJZT) and Xie-Qing-Wan (XQW). Its characteristic for treating TS is particularly by strengthening the spleen, supplemented by inhibiting the liver. The herbs in JPZDD were strictly based on the compatibility theory of TCM. Pseudostellaria heterophylla Pax, Poria cocos Wolf, and Atractylodes macrocephala Koidz could invigorate the spleen-qi. Citrus reticulata Blanco and Pinellia ternata Breit could eliminate the phlegm. Gentiana scabra Bge, Saposhnikovia divaricata Schischk, and Uncaria rhynchopylla Jacks could clear away the liver fire and calm down the liver wind. Ligusticum chuanxiong Hort and Angelica sinensis Diels could nourish the liver blood and harmonize the live wind.
Evidence based on the neurocognitive literature earlier indicated that diminished executive functions (EFs) such as working memory, cognitive flexibility are present in TS children [13, 14]. Neurotoxic species catalyzed by monoamine oxidases (MAOs) could induce mitochondrial damage and neuronal apoptosis in the prefrontal cortex and basal ganglia, the cascade of which is assumed to contribute to tics and hyperactive behavior [15, 16]. Combining with the existing studies, efficiencies of the active compounds (Table 1) in JPZDD are complicated but relatively unified. Polysaccharides, total alkaloids, and tetramethylpyrazine have been proven to ameliorate the cerebral hypoxic ischemia and restore the balance of oxidants and reductants in the cortex [17–19]. Sodium ferulate has potent protective effects against glutamate-induced neurotoxicity on developing mouse fetal brain . Rhynchophylline protects the neuronal cultures against MA exposure and promptly attenuate intracellular calcium overload triggered by MA challenge . Gentianine and senkyunolide increase the inhibitory transmitters which antagonize the excessive excitability in the brain regions [22, 23]. In brief, its anti-tics effect might partly attribute to the synergistic interactions consisting of antioxidation and cognitive improvement.
Previous studies in our group have been focused on JPZDD regulation of monoamine neurotransmitters and their metabolites in TS mice together with its efficacy on anti-tics. The findings suggested that 10 g kg−1 JPZDD (equivalence of 5-fold dosage for children) could decrease the levels of DA, DOPAC, HVA, 5-HIAA, and NE in the striatum and peripheral blood. It is tempting to discover that XQW is the predominant inhibitor acting on DA efflux. Detected by high performance liquid chromatography (HPLC), the level of DA in IDPN+XQW group is lower than the other four groups, and results of the falling percentage are 18.54% (compared with IDPN group), 21.66% (compared with IDPN+Tia group), 13.02% (compared with IDPN+JPZDD group), and 21.21% (compared with IDPN+LJZT group), respectively. Further research about the anti-tics effect of JPZDD on TS mice model has not been carried out, though it has been testified that JPZDD and XQW could reduce the times of spontaneous hyperkinesias [24, 25]. Therefore, 10-fold dosage was given in this study, and the satisfactory results were achieved. Overly rigid sequences of action were ameliorated apparently shown from the chart depicting the severity of stereotype scored at each time points. The broken line emerged as a stable downtrend in IDPN+JPZDD group, whereas a small bounce during the 3rd and 4th week in IDPN+Tia group then declined. The variability exhibited is more or less in agreement with that in clinic which reflected a long-term curative predominance of JPZDD.
Through abnormal expression of DAT exists in TS patients, it is still unclear what role it plays in formation of the disease. A much greater density of DAT may reflect the preponderance of DA innervation in together with vesicular monoamine transporter type 2, but few pros put forward which count this change as an offset to thrust of hyperdopaminergia. An animal experiment has confirmed that DAT knockdown mutant mice cause extracellular DA levels in the neostriatum to rise to 170% of wild-type control levels, and sequential super stereotypy occurs in these complex fixed action patterns of hyperdopaminergic mutant mice .
Hypothesis of supersensitive postsynaptic DA receptor (DR) is a complementary standpoint supported by the typical evidence from clinical response of TS patients to DR antagonists such as haloperidol. An intriguing phenomenon arose that reduced cerebral spinal fluid baseline and turnover levels of homovanillic acid in untreated cases recovered to normal range after drugs. By antagonizing the sites on postsynaptic DR, the binding of DR will be reduced. Early opinions suggested that chronic haloperidol treatment had a higher impact on DR than DAT, which brought about increased DRD2 specific binding but lack of an adaptative change of DAT . In a subsequent literature, we found that DRD2 could interfere with the expression and reuptake capacity of DAT by virtue of DRD2-DAT interaction, which further influenced the clearance of DA. According to this perspective, exogenous and endogenous factors may become determinants to concentration of DA in synaptic cleft secondary to reaction of momentary variation of DAT.
3,3′-iminodipropionitrile (IDPN) as a neurotoxin could produce the rodents a persistent behavior syndrome resembling TS. The IDPN-induced dyskinesia was considered due to activation of DA neurons and enhanced by administration of L-dopa, which increases DA concentration. Moreover, hyperfunction of DA neuronal system could be relieved by Tia .
Tia, acting as a selective D2R antagonist, has a supersensitive affinity for D2R in the ventral striatum and parts of the limbic system. It could antagonize the dyskinetic orolinguofacial symptoms triggered by injections of DA in the striatum which is assumed to inhibit the stimulation of DA2 neurons that cause dyskinetic reactions. A randomized, double-blind, placebo-controlled crossover study involving 17 TS children testified its significant reduction of tic symptomatology . The positive anti-tics profile with doses has also been proven in rodents , otherwise high doses (ED50 = 60 mg kg−1, i.p.) of Tia were found to decrease spontaneous locomotor activity induced by apomorphine 3 times higher than haloperidol .
Hence, in this study, IDPN and Tia were chosen as inducer and control drug in comparison with JPZDD, respectively. In line with the existing reports, the induced mice demonstrated a series of stereotyped behaviors mainly displayed as lateral and vertical head twitching, circling, sniffing, and grooming, and these symptoms lasted at least 2 months without medicine intervention. The impairment of DAT in IDPN group worsened the most sharply in four groups. JPZDD and Tia could increase the expression of DAT protein and mRNA in varying degrees.
Simultaneously, the affinity binding to radioligand tested by neuroimaging indicated JPZDD and Tia might improve the bioactivity of DAT. Combined with previous results, it is reasonable to postulate that downregulation of DAT in striatum which leads directly to higher concentration of DA is one potential pathogenesis of TS (Figure 4), and the anti-tics effect of JPZDD may be connected with upregulation of DAT expression.
Thus far, a typical drug for patients with TS targeting at DAT has not been on market due to lack of convincing clinical evidences . Currently, haloperidol and sulpiride as the representatives of first-line antipsychotics are widely accepted for their effectiveness in clinic. However, their adverse reactions such as extrapyramidal symptoms, tardive dyskinesia, drowsiness, and hyperprolactinemia usually daunt TS patients . The creation of JPZDD largely avoided the side effects above .
Some limitations existed in the course of the experiment. Firstly, on account of smaller striatum in brain tissue, we just obtain the sample as a whole where the pathological damages are hardly located precisely. Secondly, respecting a limited number of TS mice in each group, it is difficult to relate the injury severity with the degrees of behavioral scores, which could be used as a reference for judging the severity and prognosis in clinic. Thirdly, this study did not explain the phenomenon of higher expression of DAT in some TS patients.
In conclusion, JD is an effective formula for treating TS on basis of upregulating the DAT expression in the striatum, which may indirectly reinforces the recapture of DA back to the presynaptic membrane. Findings of this study also provide a new recognition that the expression of DAT in DA system is an important factor contributing to occurrence and development of TS.
The authors state that they have read and approved the paper submitted to the journal. The authors declared that they have no conflict of interests in the matter and no direct financial relation with the commercial identity mentioned in this work. D. Wang and S. Wang contributed equally to this work. This study was funded by a Grant from the National Natural Science Foundation of China (no. 30873285).
- M. H. Bloch and J. F. Leckman, “Clinical course of Tourette syndrome,” Journal of Psychosomatic Research, vol. 67, no. 6, pp. 497–501, 2009.
- M. M. Robertson, “The prevalence and epidemiology of Gilles de la Tourette syndrome—part 1: the epidemiological and prevalence studies,” Journal of Psychosomatic Research, vol. 65, no. 5, pp. 461–472, 2008.
- J. S. Stern, S. Burza, and M. M. Robertson, “Gilles de la Tourette’s syndrome and its impact in the UK,” Postgraduate Medical Journal, vol. 81, no. 95, pp. 112–119, 2005.
- C. Winter and A. Heinz, “Tourette syndrome as a neurotransmitter disorder,” in Encyclopedia of Neuroscience, pp. 1035–1040, Springer, New York, NY, USA, 2009.
- D. F. Wong, J. R. Brašić, H. S. Singer et al., “Mechanisms of dopaminergic and serotonergic neurotransmission in Tourette syndrome: clues from an in vivo neurochemistry study with PET,” Neuropsychopharmacology, vol. 33, no. 6, pp. 1239–1251, 2008.
- T. L. Wallace, G. A. Gudelsky, and C. V. Vorhees, “Methamphetamine-induced neurotoxicity alters locomotor activity, stereotypic behavior, and stimulated dopamine release in the rat,” The Journal of Neuroscience, vol. 19, no. 20, pp. 9141–9148, 1999.
- N. R. Zahniser and A. Sorkin, “Trafficking of dopamine transporters in psychostimulant actions,” Seminars in Cell and Developmental Biology, vol. 20, no. 4, pp. 411–417, 2009.
- S. R. Jones, R. R. Gainetdinov, R. M. Wightman, and M. G. Caron, “Mechanisms of amphetamine action revealed in mice lacking the dopamine transporter,” The Journal of Neuroscience, vol. 18, no. 6, pp. 1979–1986, 1998.
- L. Q. Wu, S. M. Wang, X. Cui et al., “Clinical observation of treating Tourette syndrome by combination of Liujunzi Decoction and Xieqing Pill,” Journal of Sichuan of Traditional Chinese Medicine, vol. 24, no. 10, pp. 81–83, 2006.
- B. I. Diamond, M. G. Reyes, and R. Borison, “A new animal model for Tourette syndrome,” Advances in Neurology, vol. 35, pp. 221–225, 1982.
- H. A. Khan, A. S. Alhomida, and I. A. Arif, “Neurovestibular toxicities of acrylonitrile and iminodipropionitrile in rats: a comparative evaluation of putative mechanisms and target sites,” Toxicological Sciences, vol. 109, no. 1, pp. 124–131, 2009.
- J. M. Zhang, J. H. Tian, Z. Guo et al., “Automated online preparation of 11C-β-CFT, a dopamine transporter imaging agent,” Chinese Journal of Nuclear Medicine, vol. 25, no. 3, pp. 142–145, 2005.
- D. T. Stuss and M. P. Alexander, “Executive functions and the frontal lobes: a conceptual view,” Psychological Research, vol. 63, no. 3-4, pp. 289–298, 2000.
- W. R. Kates, M. Frederikse, S. H. Mostofsky et al., “MRI parcellation of the frontal lobe in boys with attention deficit hyperactivity disorder or Tourette syndrome,” Psychiatry Research—Neuroimaging, vol. 116, no. 1-2, pp. 63–81, 2002.
- M. Bortolato, K. Chen, and J. C. Shih, “Monoamine oxidase inactivation: from pathophysiology to therapeutics,” Advanced Drug Delivery Reviews, vol. 60, no. 13-14, pp. 1527–1533, 2008.
- A. Feigin, R. Kurlan, M. P. McDermott et al., “A controlled trial of deprenyl in children with Tourette's syndrome and attention deficit hyperactivity disorder,” Neurology, vol. 46, no. 4, pp. 965–968, 1996.
- K. Duan and Y. Tang, “Effects of total alkaloids from Pinellia ternate on learning, memory and oxidative stress in Parkinson's disease rat models,” Acta Laboratorium Animalis Scientia Sinica, vol. 20, no. 2, pp. 49–52, 2012.
- Q. Ruan, X. X. He, Y. Y. Hu, and F. Li, “Effects of different components of Ligusticum chuanxiong Hort of ferulic acid and ligustrazine on the nervous system of mice,” Chinese Journal of Hospital Pharmacy, vol. 27, no. 8, pp. 1087–1090, 2007.
- Z. Q. Zhang, Y. J. Tian, and J. Zhang, “Studies on the antioxidative activity of polysaccharides from radix Saposhnikoviae,” Journal of Chinese Medicinal Materials, vol. 31, no. 2, pp. 268–272, 2008.
- L. Yu, Y. Zhang, R. Ma, L. Bao, J. Fang, and T. Yu, “Potent protection of ferulic acid against excitotoxic effects of maternal intragastric administration of monosodium glutamate at a late stage of pregnancy on developing mouse fetal brain,” European Neuropsychopharmacology, vol. 16, no. 3, pp. 170–177, 2006.
- D. D. Xu, R. Hoeven, R. Rong, and W. C. Cho, “Rhynchophylline protects cultured rat neurons against methamphetamine cytotoxicity,” Evidence-Based Complementary and Alternative Medicine, vol. 2012, Article ID 636091, 7 pages, 2012.
- C. Peng, X. Xie, L. Wang, L. Guo, and T. Hu, “Pharmacodynamic action and mechanism of volatile oil from Rhizoma Ligustici Chuanxiong Hort. on treating headache,” Phytomedicine, vol. 16, no. 1, pp. 25–34, 2009.
- Y. H. Wang, S. Liang, D. S. Xu et al., “Effect and mechanism of senkyunolide I as an anti-migraine compound from Ligusticum chuanxiong,” Journal of Pharmacy and Pharmacology, vol. 63, no. 2, pp. 261–266, 2011.
- X. Cui, L. Wei, S. M. Wang et al., “Influence and mechanism of Jianpizhidong Decoction on autonomic activities in mouse model of Tourette's syndrome,” Journal of Beijing University of Traditional Chinese Medicine (Clinical Medicine), vol. 18, no. 1, pp. 1–4, 2011.
- L. Wei, S. M. Wang, G. X. Yue et al., “Effects of Jianpizhidong Decoction on dopamine pathway in striatum of TS model mice,” Chinese Journal of Information on Traditional Chinese Medicine, vol. 16, no. 12, pp. 38–40, 2009.
- K. C. Berridge, J. W. Aldridge, K. R. Houchard, and X. Zhuang, “Sequential super-stereotypy of an instinctive fixed action pattern in hyper-dopaminergic mutant mice: a model of obsessive compulsive disorder and Tourette's,” BMC Biology, vol. 3, article 4, 2005.
- R. Rivest, P. Falardeau, and T. Di Paolo, “Brain dopamine transporter: gender differences and effect of chronic haloperidol,” Brain Research, vol. 692, no. 1-2, pp. 269–272, 1995.
- N. Ogawa, K. Mizukawa, K. Haba, and H. Sato, “Neurotransmitter and receptor alterations in the rat persistent dyskinesia model induced by iminodipropionitrile,” European Neurology, vol. 30, no. 1, pp. 31–40, 1990.
- C. Eggers, A. Rothenberger, and U. Berghaus, “Clinical and neurobiological findings in children suffering from tic disease following treatment with tiapride,” European Archives of Psychiatry and Neurological Sciences, vol. 237, no. 4, pp. 223–229, 1988.
- N. Bock, G. H. Moll, M. Wicker et al., “Early administration of tiapride to young rats without long-lasting changes in the development of the dopaminergic system,” Pharmacopsychiatry, vol. 37, no. 4, pp. 163–167, 2004.
- B. Scatton, C. Cohen, G. Perrault et al., “The preclinical pharmacologic profile of tiapride,” European Psychiatry, vol. 16, supplement 1, pp. 29s–34s, 2001.
- V. Roessner, K. J. Plessen, A. Rothenberger et al., “European clinical guidelines for Tourette syndrome and other tic disorders—part II: pharmacological treatment,” European Child and Adolescent Psychiatry, vol. 20, no. 4, pp. 173–196, 2011.
- R. A. Bressan, H. M. Jones, and L. S. Pilowsky, “Atypical antipsychotic drugs and tardive dyskinesia: relevance of D 2 receptor affinity,” Journal of Psychopharmacology, vol. 18, no. 1, pp. 124–127, 2004.
Copyright © 2013 Dao-han Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.