TY - JOUR
T1 - LY235959 attenuates development phase of Methamphetamine-Induced behavioral sensitization through the PP2A/B - AKT cascade in the dorsal striatum of C57/BL6 mice
AU - Chen, Gang
AU - Yang, Canyu
AU - Liang, Min
AU - Yin, Jianmin
AU - Gao, Baoyao
AU - Asif Nazir, Khosa
AU - Wang, Jing
AU - Xiao, Jing
AU - Shang, Qing
AU - Qian, Hongyan
AU - Qiao, Chuchu
AU - Zhang, Ping
AU - Fang, Jie
AU - Li, Tao
AU - Liu, Xinshe
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/4/17
Y1 - 2022/4/17
N2 - Drug addiction can be described as a chronic and relapsing brain disease. Behavioral sensitization is common animal model in the study of addiction and N-Methyl-D-aspartate subtype of glutamate receptor (NMDAR) is believed play key role in this process. LY235959 is a competitive NMDAR antagonist, however, its effect on methamphetamine (METH)-induced behavioral sensitization is not been reported yet. In this study, we choose three doses (0.33 mg/kg, 1.0 mg/kg, and 3.0 mg/kg) of LY235959 to investigate its effect on locomotor activity, METH-induced behavioral sensitization and different phases of it in C57/BL6 mice. We also used western blotting to examine the PP2A/B – AKT cascade which had been proved involved in METH-induced behavioral sensitization in the dorsal striatum (DS). The results showed that only 0.33 mg/kg LY235959 increased locomotor activity dramatically, however, 1.0 mg/kg and 3.0 mg/kg of LY235959 could attenuate METH-induced behavioral sensitization markedly. We also found that LY235959 only disrupted the development phase of METH-induced behavioral sensitization and the following western blotting results further indicated that PP2A/B – AKT cascade might involve in this process. Taken together, these results indicated that LY235959 attenuates development phase of METH-induced behavioral sensitization through the PP2A/B - AKT cascade in the DS.
AB - Drug addiction can be described as a chronic and relapsing brain disease. Behavioral sensitization is common animal model in the study of addiction and N-Methyl-D-aspartate subtype of glutamate receptor (NMDAR) is believed play key role in this process. LY235959 is a competitive NMDAR antagonist, however, its effect on methamphetamine (METH)-induced behavioral sensitization is not been reported yet. In this study, we choose three doses (0.33 mg/kg, 1.0 mg/kg, and 3.0 mg/kg) of LY235959 to investigate its effect on locomotor activity, METH-induced behavioral sensitization and different phases of it in C57/BL6 mice. We also used western blotting to examine the PP2A/B – AKT cascade which had been proved involved in METH-induced behavioral sensitization in the dorsal striatum (DS). The results showed that only 0.33 mg/kg LY235959 increased locomotor activity dramatically, however, 1.0 mg/kg and 3.0 mg/kg of LY235959 could attenuate METH-induced behavioral sensitization markedly. We also found that LY235959 only disrupted the development phase of METH-induced behavioral sensitization and the following western blotting results further indicated that PP2A/B – AKT cascade might involve in this process. Taken together, these results indicated that LY235959 attenuates development phase of METH-induced behavioral sensitization through the PP2A/B - AKT cascade in the DS.
KW - Behavioral sensitization
KW - LY235959
KW - Methamphetamine
KW - N-Methyl-D-aspartate receptors
KW - Protein phosphatase 2A
UR - https://www.scopus.com/pages/publications/85126270045
U2 - 10.1016/j.neulet.2022.136561
DO - 10.1016/j.neulet.2022.136561
M3 - 文章
C2 - 35240244
AN - SCOPUS:85126270045
SN - 0304-3940
VL - 776
JO - Neuroscience Letters
JF - Neuroscience Letters
M1 - 136561
ER -