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丙咪嗪长期治疗对大鼠尾状核壳核中D2多巴胺受体生物合成及功能特性的影响。

The effect of prolonged treatment with imipramine on the biosynthesis and functional characteristics of D2 dopamine receptors in the rat caudate putamen.

作者信息

Dziedzicka-Wasylewska M, Rogoz R

机构信息

Department of Pharmacology, Institute of Pharmacology, Polish Academy of Sciences, Kraków.

出版信息

Br J Pharmacol. 1998 Mar;123(5):833-8. doi: 10.1038/sj.bjp.0701681.

Abstract
  1. The present study shows the effects of imipramine in a single dose (10 mg kg(-1), p.o.) or following repeated (14 days, twice a day) treatment on the level of mRNA coding for D2 dopamine receptors in the rat caudate putamen (CP). Repeated administration of imipramine resulted in the increase of the level of mRNA coding for D2 dopamine receptors. 2. Radioligand binding studies with the D2 receptor agonist, [3H]-N-0437, indicated, that following imipramine administration, the affinity of the agonist for the D2 dopamine receptor significantly increased, though without any alterations in the Bmax. 3. Pharmacological manipulations (by use of forskolin, GppNHp and quinpirole) of the cyclic AMP generating system, ex vivo following administration of imipramine indicated that an up-regulation of factors inhibiting cyclic GMP formation takes place. 4. Most probably it is the D2 dopamine receptor which undergoes functional up-regulation, resulting from the enhancement of its biosynthesis.
摘要
  1. 本研究显示了单次剂量(10毫克/千克,口服)或重复(14天,每日两次)给予丙咪嗪对大鼠尾状核壳核(CP)中编码D2多巴胺受体的mRNA水平的影响。重复给予丙咪嗪导致编码D2多巴胺受体的mRNA水平升高。2. 用D2受体激动剂[3H]-N-0437进行的放射性配体结合研究表明,给予丙咪嗪后,激动剂对D2多巴胺受体的亲和力显著增加,尽管最大结合容量(Bmax)没有任何改变。3. 在给予丙咪嗪后,对环磷酸腺苷(cAMP)生成系统进行药理学操作(使用福斯可林、鸟苷-5'-三磷酸(GppNHp)和喹吡罗),体外实验表明,抑制环磷酸鸟苷(cGMP)形成的因子发生了上调。4. 很可能是D2多巴胺受体发生了功能性上调,这是由于其生物合成增强所致。

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