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大鼠前岛叶皮质中的多巴胺受体调节长期伤害感受。

Dopamine receptors in the anterior insular cortex modulate long-term nociception in the rat.

作者信息

Coffeen Ulises, López-Avila Alberto, Ortega-Legaspi J Manuel, del Angel Rosendo, López-Muñoz Francisco J, Pellicer Francisco

机构信息

Laboratorio de Neurofisiología Integrativa, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de Fuente, Camino a Xochimilco 101, San Lorenzo Huipulco, Tlalpan, México D.F. CP. 14370, Mexico.

出版信息

Eur J Pain. 2008 Jul;12(5):535-43. doi: 10.1016/j.ejpain.2007.08.008. Epub 2007 Oct 23.

Abstract

The rostral agranular insular cortex (RAIC) receives dopaminergic projections from the mesolimbic system, which has been involved in the modulation of nociceptive processes. In this study we determined the contribution of dopamine D(1) and D(2) receptors in the RAIC regarding nociception processing in a neuropathic pain model, as well as inflammatory articular nociception measured as pain-induced functional impairment in the rat (PIFIR). Microinjection of vehicle or substances into the RAIC was performed after the induction of nociception. The groups were treated with: a dopamine D(1) receptor antagonist (SCH-23390), a dopamine D(1) receptor agonist (SKF-38393), a dopamine D(2) receptor agonist (TNPA) and a dopamine D(2) receptor antagonist (spiperone). Chronic nociception, induced by denervation, was measured by the autotomy score in which onset and incidence were also determined. The SCH-23390 and TNPA groups showed a decrease in the autotomy score and a delay on the onset as compared to control, whereas the PIFIR groups did not show statistical differences. This work shows the differential role of dopamine receptors within the RAIC in which the activation of D(2) or the blockade of D(1) receptors elicit antinociception.

摘要

喙部无颗粒岛叶皮质(RAIC)接受来自中脑边缘系统的多巴胺能投射,该系统参与伤害性感受过程的调节。在本研究中,我们确定了在神经性疼痛模型中,RAIC内多巴胺D(1)和D(2)受体在伤害性感受处理方面的作用,以及以大鼠疼痛诱导功能损害(PIFIR)衡量的炎性关节伤害性感受。在诱导伤害性感受后,将载体或物质微量注射到RAIC中。各实验组接受以下处理:一种多巴胺D(1)受体拮抗剂(SCH - 23390)、一种多巴胺D(1)受体激动剂(SKF - 38393)、一种多巴胺D(2)受体激动剂(TNPA)和一种多巴胺D(2)受体拮抗剂(螺哌隆)。通过自残评分来测量由去神经支配诱导的慢性伤害性感受,同时确定其发作情况和发生率。与对照组相比,SCH - 23390组和TNPA组的自残评分降低且发作延迟,而PIFIR组未显示出统计学差异。这项研究表明RAIC内多巴胺受体具有不同作用,其中D(2)受体的激活或D(1)受体的阻断可引发抗伤害感受作用。

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