首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Modulation of dopamine uptake in rat nucleus accumbens: effect of specific dopamine receptor antagonists and sigma ligands.
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Modulation of dopamine uptake in rat nucleus accumbens: effect of specific dopamine receptor antagonists and sigma ligands.

机译:大鼠伏隔核中多巴胺摄取的调节:特定多巴胺受体拮抗剂和西格玛配体的作用。

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摘要

The ability of dopamine (DA) antagonists and sigma receptor ligands to alter [(3)H]-DA uptake was examined using synaptosomes prepared from the nucleus accumbens of female rats. Pre-incubation with compounds having a high affinity for sigma (rimcazole, haloperidol, and spiperone) receptors produced dose dependent inhibition of (3)H-DA uptake. Sulpiride, a pure DA D(2) antagonist had no effect. In contrast, DA uptake was potentiated in response to (+)-3-(3-hydroxyphenyl)-N-(1-propyl)piperidine, a mixed sigma receptor antagonist and DA D(2) receptor agonist. Similarly, SKF-10,047, a selective sigma receptor agonist, and progesterone, a putative endogenous ligand for the sigma receptor, produced significant increases in (3)[H]-DA uptake. These data suggest a potential role for sigma and DA ligands in the regulation of DA uptake in the nucleus accumbens.
机译:使用由雌性大鼠伏伏核制备的突触小体检查了多巴胺(DA)拮抗剂和sigma受体配体改变[[3)H] -DA摄取的能力。与对sigma(rimcazole,氟哌啶醇和spiperone)受体具有高亲和力的化合物进行预温育可产生剂量依赖性的(3)H-DA吸收抑制作用。舒必利,纯DA D(2)拮抗剂无效。相反,响应于(+)-3-(3-羟苯基)-N-(1-丙基)哌啶(一种混合的sigma受体拮抗剂和DA D(2)受体激动剂),DA吸收得到增强。同样,选择性sigma受体激动剂SKF-10,047和sigma受体的假定内源性配体孕酮使(3)[H] -DA吸收显着增加。这些数据表明西格玛和DA配体在伏伏核吸收DA的调节中的潜在作用。

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