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- W3032453453 abstract "ObjectiveTo explore curative effect, effective dose and its possible mechanisms of dopamine D3 receptor (DAD3R) agonist BP897 in treatment of mice with tourette syndrome(TS).MethodsAccording to random number table, random number table method, a total of 60 healthy male ICR mice were average divided into 6 groups(n=10 for each group): model group, BP897Ⅰ, Ⅱ, Ⅲ group, positive control group and normal control group.Except normal control group, the other 5 groups were established mice model of TS.Intragastric administration to mice every day from 8th day of experiment: normal control group and model group with 0.1 mL normal saline ; positive control group with haloperidol 0.5 mg/kg; BP897Ⅰ, Ⅱ, Ⅲ group with BP897 0.3, 1.0, 3.0 mg/kg. Upon successful established TS mice model immediately, 7th and 28th of intragastric administration, stereotyped behavior scores of mice were got in double-blind way.On the 28th day of intragastric administration, DAD3R, dopamine transporter(DAT) and dopamine contents in mice brain tissues were detected by enzyme-linked immunosorbent assay(ELISA), and use statistical methods to compare differences of stereotyped behavior scores, DAD3R, DAT and dopamine contents among different groups, and analyze relationship between DAD3R and dopamine, DAT and dopamine.There were no significant differences among 6 groups in general conditions, such as body weight(P>0.05).Results①Comparison of stereotyped behavior scores of mice on 7th day and 28th day of intragastric administration: BP897Ⅱ and Ⅲ group were significantly lower than those in model group, respectively, BP897Ⅱ group were significantly lower than those in BP897Ⅰ group, and BP897Ⅲ group were significantly lower than those in BP897Ⅱ group, too, and the differences were significant(P 0.05). ②Comparison of DAD3R, DAT and dopamine contents in mice brain tissues on 28th day of intragastric administration: Model group were significantly lower than those in BP897Ⅲ group, positive control group and normal control group, respectively, and in BP897Ⅲ group were significantly lower than those in positive control group, too, and the differences were significant(P 0.05). ③DAD3R and DAT contents in mice brain tissues were both positively correlated with dopamine content(r=0.765, 0.766; P<0.001).Conclusions1.0-3.0 mg/kg dose of BP897 can treat mice with TS effectively, and 3.0 mg/kg dose of BP897 can much better control the stereotyped behavior of mice with TS, which can reach the same curative effect with haloperidol.Key words: BP897; Tourette syndrome; Receptors, dopamine D3; Dopamine plasma membrane transport proteins; Dopamine; Mice, inbred ICR" @default.
- W3032453453 created "2020-06-05" @default.
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- W3032453453 date "2015-06-01" @default.
- W3032453453 modified "2023-09-23" @default.
- W3032453453 title "Study on curative effect and possible mechanisms of dopamine D3 receptor agonist BP897 in treatment of mice with tourette syndrome" @default.
- W3032453453 doi "https://doi.org/10.3877/cma.j.issn.1673-5250.2015.03.006" @default.
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