Fredholm B B, Zahniser N R, Weiner G R, Proctor W R, Dunwiddie T V
Eur J Pharmacol. 1985 Apr 23;111(1):133-6. doi: 10.1016/0014-2999(85)90123-2.
In a dose of 0.1 mg/kg, PIA had marked behavioural effects in long-sleep mice (which show a high sensitivity to ethanol, while no significant effect was observed in short sleep mice (low sensitivity to ethanol). The number of [3H]PIA binding sites in cortex and subcortical brain regions was significantly higher in long-sleep than in short-sleep mice. The KD value was higher in cortex and cerebellum in the short-sleep mice, but there were no differences in the number of hippocampal beta-adrenoceptors or in the adenosine analogue-induced increase in cyclic AMP accumulation in slices of mouse hippocampus.
以0.1毫克/千克的剂量给药时,PIA对长睡眠小鼠(对乙醇高度敏感)有显著的行为影响,而在短睡眠小鼠(对乙醇低敏感)中未观察到显著影响。长睡眠小鼠皮层和皮层下脑区的[3H]PIA结合位点数量明显高于短睡眠小鼠。短睡眠小鼠皮层和小脑中的KD值较高,但海马β-肾上腺素能受体数量或腺苷类似物诱导的小鼠海马切片中环磷酸腺苷积累增加方面没有差异。