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多巴胺D(3)受体缺陷小鼠给予精神兴奋剂和抗精神病药物后神经降压素基因表达及行为反应

Neurotensin gene expression and behavioral responses following administration of psychostimulants and antipsychotic drugs in dopamine D(3) receptor deficient mice.

作者信息

Betancur C, Lépée-Lorgeoux I, Cazillis M, Accili D, Fuchs S, Rostène W

机构信息

INSERM U. 339, Hôpital Saint-Antoine, Paris, France.

出版信息

Neuropsychopharmacology. 2001 Feb;24(2):170-82. doi: 10.1016/S0893-133X(00)00179-2.

Abstract

Exposure to psychostimulants and antipsychotics increases neurotensin (NT) gene expression in the striatum and nucleus accumbens. To investigate the contribution of D(3) receptors to these effects we used mice with targeted disruption of the D(3) receptor gene. Basal NT mRNA expression was similar in D(3) receptor mutant mice and wild-type animals. Acute administration of haloperidol increased NT gene expression in the striatum in D(3)+/+, D(3)+/- and D(3)-/- mice. Similarly, acute cocaine and amphetamine induced NT mRNA expression in the nucleus accumbens shell and olfactory tubercle to a comparable extent in D(3) mutants and wild-type mice. Daily injection of cocaine for seven days increased NT mRNA in a restricted population of neurons in the dorsomedial caudal striatum of D(3)+/+ mice, but not in D(3)-/- and D(3)+/- animals. No differences were observed between D(3) receptor mutant mice and wild-type littermates in the locomotor activity and stereotyped behaviors induced by repeated cocaine administration. These findings demonstrate that dopamine D(3) receptors are not necessary for the acute NT mRNA response to drugs of abuse and antipsychotics but appear to play a role in the regulation of NT gene induction in striatal neurons after repeated cocaine. In addition, our results indicate that the acute locomotor response to cocaine and development of psychostimulant-induced behavioral sensitization do not require functional D(3) receptors.

摘要

接触精神兴奋剂和抗精神病药物会增加纹状体和伏隔核中神经降压素(NT)的基因表达。为了研究D(3)受体对这些作用的贡献,我们使用了D(3)受体基因靶向破坏的小鼠。D(3)受体突变小鼠和野生型动物的基础NT mRNA表达相似。在D(3)+/+、D(3)+/-和D(3)-/-小鼠中,急性给予氟哌啶醇会增加纹状体中的NT基因表达。同样,急性给予可卡因和苯丙胺在D(3)突变小鼠和野生型小鼠中诱导伏隔核壳和嗅结节中NT mRNA表达的程度相当。连续七天每天注射可卡因会增加D(3)+/+小鼠背内侧尾状纹状体中特定神经元群体的NT mRNA,但在D(3)-/-和D(3)+/-动物中则不会。在重复给予可卡因诱导的运动活动和刻板行为方面,未观察到D(3)受体突变小鼠与野生型同窝小鼠之间存在差异。这些发现表明,多巴胺D(3)受体对于滥用药物和抗精神病药物引起的急性NT mRNA反应并非必需,但在重复给予可卡因后,似乎在调节纹状体神经元中NT基因诱导方面发挥作用。此外,我们的结果表明,对可卡因的急性运动反应以及精神兴奋剂诱导的行为敏化的发展并不需要功能性D(3)受体。

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