Methanol extract from radix of Glycyrrhizae uralensis attenuate methamphetamine-induced hyperlocomotor activity

Background and objective: Methamphetamine (Meth) is a widely abused psychostimulant that produces hyperlocomotion in rodents. Radix of Glycyrrhizae uralensis comprises a variety of bioactive components that have neuroprotective effects. In a previous study, we have demonstrated methanol extracts from radix of Glycyrrhizae uralensis (MEGR) suppress acute cocaine-induced extracellular dopamine release in the nucleus accumbens. In the present study, we investigated the effect of MEGR on acute Meth-induced hyperlocomotion. Methods: Male Sprague–Dawley rats were orally administered with MEGR (60 mg/kg and 180 mg/kg) 60 min prior to an intraperitoneal injection of Meth (1.0 mg/kg). Results: Behavioral analysis showed acute Meth greatly increased locomotor activities, while pretreatment 대한한의학 방제학회지 제22권 제1호 (2014년 6월) Herbal Formula Science(HFS) 2014;22(1):105~112 106 with MEGR dose dependently inhibited the hyperlocomotion. In parallel, there were markedly increased levels of dopamine and its metabolite 3, 4-dihydroxyphenylacetic acid in the nucleus accumbens tissues in Meth-treated rats, which were also almost completely reversed by 180 mg/kg MEGR. Conclusions: These results showed that radix of Glycyrrhizae uralensis attenuates Meth-induced hyperlocomotion by inhibiting dopamine synthesis and utilization, suggesting that radix of Glycyrrhizae uralensis might be effective in blocking the rewarding effect of Meth. Keyword : Methamphetamine, Glycyrrhizae uralensis, Locomotion, Dopamine, Nucleus accumbens

with MEGR dose dependently inhibited the hyperlocomotion.In parallel, there were markedly increased levels of dopamine and its metabolite 3, 4-dihydroxyphenylacetic acid in the nucleus accumbens tissues in Meth-treated rats, which were also almost completely reversed by 180 mg/kg MEGR.
Conclusions: These results showed that radix of Glycyrrhizae uralensis attenuates Meth-induced hyperlocomotion by inhibiting dopamine synthesis and utilization, suggesting that radix of Glycyrrhizae uralensis might be effective in blocking the rewarding effect of Meth.Although methamphetamine (Meth) dependence is a serious worldwide public health problem with major medical, psychiatric, socioeconomic and legal consequences [1], there is currently no FDA approved pharmacotherapy for this addictive disorder.The rewarding effects of Meth including euphoria and many other psychostimulant effects are the mainstay to sustain the continued use of Meth, ultimately lead to Meth addition [2].Therefore, nullifying the rewarding effects of Meth is a promising approach to treat Meth addition.
It is well documented that the commonly abused psychostimulants including Meth increase locomotor activity in rodents, and the biological mechanisms of this stimulant action are homologous with their rewarding effects [3].Convincing evidence shows that the rewarding effects of Meth mainly come from enhanced dopaminergic neurostransmissions in the mesolimbic and mesocortical brain regions such as the ventral tegmental area, the nucleus accumbens (Nacc) and the medial prefrontal cortex, which also mediate Meth-induced hyperlocomotion [4].Therefore, inhibition on the increased dopaminergic activities in the mesolimbic brain regions biochemically prevents the formation of the biological bases for Meth addiction and behaviorally blocks hyperlocomotion induced by Meth.For example, a selective dopamine (DA) 1 receptor antagonist SCH23390 injection into the Nacc attenuates Meth-induced hyperlocomotion in rats [5], Limonene inhibits Meth-induced increased locomotor activity via regulation of enhanced accumbal DA release [6].
Radix of Glycyrrhizae uralensis (G.radix), one of the oldest and most popularly used botanicals in traditional Oriental medicine, contains flavonoids and pentacyclic triterpene saponin as major constituents, which include liquiritigenin, isoliquiritigenin, liquiritin, liquiritin apioside, and glycyrrihizin [7].Being an important tonic, G. radix is generally used to replenish and invigorate deficient Qi and blood, and widely recommended for life-enhancing properties and cure of injury or swelling and for detoxification [8].Historically, most experimental studies on pharmacological values of G. radix were devoted to its anti-inflammatory and anti-oxidative properties [9,10]    Meth (purity > 98%, obtained from Korean Food and Drug Administration) was dissolved in saline and administered intraperitoneally (i.p.) to rats in a single dose of 1.0 mg/kg.MEGR (60 and 180 mg/kg) or the vehicle was acutely applied to rats 60 min prior to Meth administration.
After MEGR (or vehicle) administration, each rat was allowed to adapt the locomotor testing box for 60 min followed by Meth administration, Ⅲ. Results

Ⅳ. Discussion
In a previous study we demonstrated MEGR suppresses cocaine-induced extracellular dopamine release in rat Nacc [12], in the present study

Flow rate: 1
.0 mL/min, column: Waters XTerrat TM RP18(150 × 4.6 mm, 5 μm) neuroprotective effects of G. radix and its bioactive ingredients against various noxious stimuli [11].Most notably, studies done in our lab have shown that methanol extracts of G. radix (MEGR) and isoliquiritigenin suppress cocaine-induced extracellular dopamine release in rat Nacc through GABAb receptors [12], and isoliquiritigenin also prevents Meth-induced neurotoxicity in mouse brain by inhibiting NF-kB activation [13].These observations conjunction with its neuroprotective effects reported by others lead to a hypothesis that G. radix have preventive effects against Meth-induced psychostimulant effects.To test this hypothesis, in the present study we evaluate the effects of MEGR on locomotor activities and accumbal DA and 3, 4dihydroxyphenylacetic acid (DOPAC) levels in rats following an acute Meth administration.Ⅱ. Materials and methods 1. Preparation of MEGR The air-dried G. radix was purchased from Daewon Pharmacy (Daegu, Republic of Korea), and its identity and composition was confirmed by Professor Sang Chan Kim of the College of Oriental Medicine at Daegu Haany University in Korea.The G. radix was crushed into powder and extracted with methanol three times for 12 h each at room temperature.The extract was filtered through a 0.2 μm filter (Nalgene, NY, USA), evaporated under reduced pressure at temperature of 37 °C and lyophilized.The amount of extracts was estimated from the dry weight of lyophilized powder, and the yield was 15.39%, and the high performance liquid chromatography (HPLC) fingerprint of MEGR is shown in Fig. 1.The MEGR was dissolved in 5% Tween-80 and orally administered.
2. Reagents Sodium octanesulfonic acid acetonitrile, tetrahydrofurane, DA and DOPAC were purchased from Sigma Co. (St Louis, MO, USA).All other drugs were of analytical or HPLC grade.3. Animals and experimental design Adult male Sprague-Dawley rats (250-270 g) were obtained from Hyochang Science (Hyuchang, Pusan, South Korea), and housed under a controlled environment with food and water ad libitum throughout the course of the study.All animal procedures were approved by the Institutional Animal Care and Use Committee for the National Institutes of Health guidelines concerning the Care and Use of Laboratory Animals.

Figure 2 .
Figure 2. Diagrammatic representation of a coronal section showing the Nacc.

Meth-induced locomotor activity Figure. 3
Figure. 3 shows the effect of MEGR on locomotor activities.ANOVA on data from MEGR treatment revealed a significant effect [F (3, 20) = 17.8, p < 0.001].Post hoc comparisons revealed acute Meth significantly increased locomotor activities in rats (vehicle+saline vs. vehicle+Meth, p < 0.001), while pretreatment with both doses of MEGR significantly inhibited the Meth-induced hyperlocomotion (vehicle+Meth

Figure 4 .
Figure 4. Effects of MEGR on the locomotor activities of saline-treated rats.Rats were treated with a single dose of saline 60 min after an acute 60 mg/kg or 180 mg/kg MEGR, and then the traveled distance of each rat was measured for 60 min immediately after the saline.Data represent mean ± SEM (n = 6/group).Vehi: vehicle, S: saline.Statistical analysis showed no difference among the groups.

Fig. 5 .
Fig. 5. shows the effects of MEGR on accumbal levels of DA and DOPAC.ANOVA and post hoc analysis showed a single dose of Meth (1 mg/kg) significantly increased both DA [F (3, 20) = 6.2, p < 0.01; vehicle+saline vs. vehicle+Meth, p < 0.01] and DOPAC [F (3, 20) = 7.5, p < 0.01; vehicle+saline vs. vehicle+Meth, p < 0.01] concentrations in the Nacc, indicating the enhanced synthesis and utilization of DA.However, similar to the behavioral results, pretreatment with 180 mg/kg MEGR significantly we extended this result showing that MEGR inhibits acute Meth-induced hyperlocomotion in rats.In the current study, the behavioral experiment revealed pretreatment with 60 mg/kg and 180 mg/kg MEGR dose-dependently attenuated Methinduced enhanced locomotor activities in rats, in addition, the neurochemical analysis exhibited 180 mg/kg MEGR almost completely blocked the acute Meth-induced increase of accumbal DA and DOPAC levels.These findings suggest that MEGR blocks Meth-induced hyperlocomtion through inhibiting elevated DA synthesis and utilization in the Nacc.Convincing evidence has highlighted the pharmaceutical values of extracts from traditional Oriental herbals in treating abused drug disorders, in particular, several laboratories have reported extracts of tonic herbals have preventive effects against the rewarding effects of abused drugs [15].For example, Kim et al. [16] have reported ginsenosides Rb1 and Rg1 blocks Meth-induced behavioral hyperactivity and conditioned place preference (CPP) in rats, Mattioli et al. [17] have demonstrated a Rhodiola rosea L. hydroalcoholic extract prevents establishment of morphine-induced CPP and facilitates extinction of established CPP.In the present study pretreatment with MEGR prevents Meth-induced hyperlocomotion related to the rewarding effects of Meth.This result suggests that MEGR may have therapeutic effects against Meth addition.Administration of Meth increases extracellular DA levels [18] in the Nacc by (1) up-regulating tyrosine hydroxylase, the rate-limiting step in DA synthesis, (2) inducing reverse transport of monoamines, (3) blocking the activity of the intracellular vesicular monoamine transporter 2, (4) decreasing the expression of the DA transporter (DAT) at the cell surface [19, 20].The released DA activates DA receptors on accumbenal GABAergic medium spiny neurons and promotes sensitivities of DA receptors, which appear to be the main biological basis for Meth-induced hyperlocomotion and rewarding effects [21].Therefore, either inhibiting DA release or dampening DA sensitivity in the Nacc can counteract psychostimulant effects of Meth on locomotion, further abrogate rewarding effects of Meth.In the above mentioned study, Kim et al. have also demonstrated the therapeutic effect of ginsenosides on Meth-induced behavioral abnormalities is mediated by inhibiting accumbenal postsynaptic DA receptors supersensitivity [16]; in another study, Egecioglu et al. have reported the glucagonlike peptide 1 agonist exendin-4 attenuates cocaine-induced hyperlocomotion by reducing accumbal DA release [22].In a previous study we demonstrated that MEGR can suppress acute cocaine-induced increase of extracellular DA release in the Nacc [12].In the current study, we found pretreatment with MEGR almost completely reversed acute Meth-induced enhanced DA synthesis and utilization in rat accumbal tissues.Taken together, these results suggest that the blockade effect of MEGR on Meth-induced hyperlocomotion may be mediated through inhibiting accumbenal DA synthesis and utilization.In summary, in the present study, we have found pretreatment with MEGR significantly attenuates acute Meth-induced hyperlocomotion and inhibits Meth-induced enhanced DA synthesis and utilization in the Nacc.These results suggest that MEGR may be effective in treating Meth addiction, possibly by modulating DAergic neurotransmissions in the Nacc.