Whitton P, Curzon G
Department of Neurochemistry, Institute of Neurology, London, UK.
Psychopharmacology (Berl). 1990;100(1):138-40. doi: 10.1007/BF02245806.
1-(3-Chlorophenyl) piperazine (mCPP) was previously shown to have an anxiogenic-like effect, i.e., it decreased total interaction in a rat social interaction test. Evidence indicated mediation by activation of 5-HT1C receptors with an ED50 of approximately 500 micrograms/kg IP (Kennett et al. 1989). A comparable effect is now shown on infusing 4 micrograms of the drug ICV or infusing 0.5 microgram into the hippocampus. Both responses were dose dependent. Infusion of 1 microgram mCPP into the amygdala had no effect. None of the above treatments significantly reduced locomotion. Results are consistent with the postulated role of the hippocampus in anxiety.
1-(3-氯苯基)哌嗪(mCPP)先前已被证明具有类焦虑作用,即在大鼠社交互动试验中它会减少总的互动行为。有证据表明其作用是通过激活5-HT1C受体介导的,腹腔注射的半数有效剂量(ED50)约为500微克/千克(肯尼特等人,1989年)。现在发现,向脑室内注射4微克该药物或向海马体注射0.5微克会产生类似的效果。两种反应均呈剂量依赖性。向杏仁核注射1微克mCPP则没有效果。上述任何一种处理均未显著降低运动能力。这些结果与海马体在焦虑中所假定的作用相符。