首页> 外文期刊>Naunyn-Schmiedeberg's Archives of Pharmacology >The neurotensin receptor antagonist SR 142948A blocks the efflux of dopamine evoked in nucleus accumbens by neurotensin ejection into the ventral tegmental area.
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The neurotensin receptor antagonist SR 142948A blocks the efflux of dopamine evoked in nucleus accumbens by neurotensin ejection into the ventral tegmental area.

机译:神经降压素受体拮抗剂SR 142948A通过将神经降压素喷射到腹侧被盖区来阻止伏伏核诱发的多巴胺流出。

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摘要

The neuropeptide neurotensin (NT) exerts a wide range of central and peripheral effects. In particular, ejection of NT (10(-7) M, 65 nl) into the ventral tegmental area (VTA) in anaesthetised rats pre-treated with pargyline increases the dopamine (DA) efflux within the nucleus accumbens (NAcc) as measured by differential pulse amperometry (DPA) combined with carbon fibre electrodes. However, this effect is not blocked by systemic pre-treatment with the potent and selective non-peptide NT receptor antagonists SR 48692 and SR 142948A, at any dose studied. The present study was designed to determine the ability of these NT receptor antagonists to block the increase in DA efflux evoked within the NAcc when they are locally applied with the peptide into the VTA. The competitive N-methyl- D-aspartate (NMDA) receptor antagonist, 2-amino-5-phosphonopentanoic acid (AP-5), applied into the VTA 1 min before NMDA, blocked the effect of NMDA on DA efflux concentration and volume dependently, thus demonstrating the suitability of our experimental procedure for characterizing both an agonist and an antagonist specific for receptors present on mesencephalic dopaminergic neurons and involved in the regulation of DA efflux within the NAcc. Intra-VTA application of SR 142948A blocked the NT-evoked increase in DA efflux within the NAcc dose dependently whereas SR 48692, at the concentration used, was inactive. These results suggest that NT regulates mesencephalic dopaminergic activity through NT receptors sensitive to SR 142948A, but possibly not to SR 48692.
机译:神经肽神经降压素(NT)发挥广泛的中枢和外周作用。尤其是,在用Pargyline预处理的麻醉大鼠中,将NT(10(-7)M,65 nl)喷射到腹侧被盖区(VTA)中,可增加伏隔核(NAcc)中多巴胺(DA)的外排,其测量方法为差动脉冲安培计(DPA)与碳纤维电极组合。但是,在任何研究剂量下,用有效的和选择性的非肽NT受体拮抗剂SR 48692和SR 142948A进行系统预处理都不会阻止这种作用。本研究旨在确定当这些NT受体拮抗剂与肽局部应用到VTA中时,它们阻断NAcc内引起的DA外排增加的能力。竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂2-氨基-5-膦基戊酸(AP-5)在NMDA之前1分钟施用到VTA中,从而阻断了NMDA对DA外排浓度和体积的影响。 ,因此证明了我们的实验程序适用于表征对中脑多巴胺能神经元上存在的受体和对NAcc内DA流出的调节具有特异性的激动剂和拮抗剂。 SR 142948A的VTA内应用可在NAcc剂量内阻断NT引起的DA流出增加,而SR 48692在所用浓度下则无效。这些结果表明,NT通过对SR 142948A(但对SR 48692不敏感)的NT受体调节中脑多巴胺能活性。

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