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丙咪嗪在大鼠纹状体切片中的神经元内作用位点。

Intraneuronal site of action for imipramine in rat striatal slices.

作者信息

Daniels A J, Gysling K, Arqueros L

出版信息

J Neurochem. 1980 Sep;35(3):718-22. doi: 10.1111/j.1471-4159.1980.tb03711.x.

Abstract

The uptake of 3H-labeled imipramine ([3H]IMI) in rat carpus striatum slices was found to be strongly temperature-dependent. The accumulation was shown to be saturable and two apparent Km's were found: 2.2 x 10(-8) and 3.5 x 10(-7) M. Once incorporated, the labeled drug was released from superfused slices by K+ (55 mM) depolarization in the presence of calcium ions. Imipramine was also studied for its ability to induce the release of [3H]dopamine ([2H]DA) which had been previously accumulated by striatal slices. It was found that striatal slices superfused during 1 or 6 min with imipramine (10(-6) - 10(-4) M) release substantial amounts of radioactive dopamine, independently of the presence of Ca2+ in the medium. This release is completely abolished after reserpine pretreatment. It is proposed that imipramine enters the dopaminergic storage vesicles and displaces dopamine. An intraneuronal mechanism of action for imipramine is discussed.

摘要

研究发现,大鼠纹状体切片对3H标记的丙咪嗪([3H]IMI)的摄取强烈依赖于温度。这种积累表现出饱和性,并且发现了两个表观Km值:2.2×10(-8)和3.5×10(-7)M。一旦掺入,在钙离子存在的情况下,通过K +(55 mM)去极化可使标记药物从灌流切片中释放出来。还研究了丙咪嗪诱导纹状体切片先前积累的[3H]多巴胺([2H]DA)释放的能力。结果发现,用丙咪嗪(10(-6)-10(-4)M)灌流1或6分钟的纹状体切片会释放大量放射性多巴胺,而与培养基中Ca2+的存在无关。利血平预处理后,这种释放完全被消除。有人提出,丙咪嗪进入多巴胺能储存囊泡并取代多巴胺。文中讨论了丙咪嗪的神经元内作用机制。

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