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Gamma-Hydroxybutyrate and Cocaine Administration Increases mRNA Expression of Dopamine D1 and D2 Receptors in Rat Brain

机译:γ-羟丁酸和可卡因给药可增加大鼠脑中多巴胺D1和D2受体的mRNA表达

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The effects of acute and repeated gamma-hydroxybutyrate (GHB) and cocaine administration on D1 and D2 dopamine receptor mRNA expression were examined using in situ hybridization histochemistry in different rat brain structures rich in GHB receptors. Six hours after a single GHB administration (500 mg/kg IP), an increase in D1 and D2 mRNA expression was observed in almost all regions examined; whereas, acute cocaine injection (20 mg/kg IP) had no effect. Repeated exposure to GHB (500 mg/kg IP twice daily) for 10 days, followed by a 14-h withdrawal period, induced increasing effects on D1 and D2 dopamine receptor mRNA expression, similar to those caused by chronic treatment with cocaine (20 mg/kg IP once a day). These effects of GHB and cocaine on dopamine receptor mRNA expression could be a consequence, for both compounds, of the modulation of dopaminergic activity; thus, supporting the benefit of GHB in cocaine substitution therapy.
机译:使用原位杂交组织化学方法,在富含GHB受体的不同大鼠脑结构中,检查了急性和反复性的γ-羟基丁酸(GHB)和可卡因对D1和D2多巴胺受体mRNA表达的影响。单次施用GHB(500 mg / kg IP)六小时后,几乎在所有检查的区域都观察到D1和D2 mRNA表达增加。急性可卡因注射(20 mg / kg IP)无效。反复暴露于GHB(500 mg / kg IP,每天两次,连续10天),然后停药14小时,诱导对D1和D2多巴胺受体mRNA表达的增加作用,类似于可卡因(20 mg慢性治疗)引起的作用/ kg IP,每天一次)。对于这两种化合物,GHB和可卡因对多巴胺受体mRNA表达的这些影响可能是调节多巴胺能活性的结果。因此,支持了GHB在可卡因替代疗法中的益处。

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