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边缘下皮质中的代谢型谷氨酸5受体有助于健康动物和患有关节炎动物的下行性疼痛易化。

Metabotropic glutamate 5 receptor in the infralimbic cortex contributes to descending pain facilitation in healthy and arthritic animals.

作者信息

David-Pereira A, Puga S, Gonçalves S, Amorim D, Silva C, Pertovaara A, Almeida A, Pinto-Ribeiro F

机构信息

Life and Health Sciences Research Institute (ICVS), School of Health Sciences (ECS), Campus of Gualtar, University of Minho, 4750-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.

Biomedicum Helsinki, Institute of Biomedicine/Physiology, University of Helsinki, Helsinki, Finland.

出版信息

Neuroscience. 2016 Jan 15;312:108-19. doi: 10.1016/j.neuroscience.2015.10.060. Epub 2015 Nov 6.

Abstract

The involvement of the prefrontal cortex in pain processing has been recently addressed. We studied the role of the infralimbic cortex (IL) and group I metabotropic glutamate receptors (mGluRs) in descending modulation of nociception in control and monoarthritic (ARTH) conditions. Nociception was assessed using heat-induced paw withdrawal while drugs were microinjected in the IL of rats. Local anesthesia of the IL or the adjacent prelimbic cortex (PL) facilitated nociception, indicating that IL and PL are tonically promoting spinal antinociception. Phasic activation with glutamate (GLU) revealed opposing roles of the PL and IL; GLU in the PL had a fast antinociceptive action, while in the IL it had a slow onset pronociceptive action. IL administration of a local anesthetic or GLU produced identical results in ARTH and control animals. An mGluR5 agonist in the IL induced a pronociceptive effect in both groups, while mGluR5 antagonists had no effect in controls but induced antinociception in ARTH rats. Activation of the IL mGluR1 (through co-administration of mGluR1/5 agonist and mGluR5 antagonist) did not alter nociception in controls but induced antinociception in ARTH animals. IL administration of an mGluR1 antagonist failed to alter nociception in either experimental group. Finally, mGluR5 but not mGluR1 antagonists blocked the pronociceptive action of GLU in both groups. The results indicate that IL contributes to descending modulation of nociception. mGluR5 in the IL enhance nociception in healthy control and monoarthritic animals, an effect that is tonic in ARTH. Moreover, activation of IL mGluR1s attenuates nociception following the development of monoarthritis.

摘要

前额叶皮质在疼痛处理中的作用最近已得到探讨。我们研究了在对照和单关节炎(ARTH)条件下,边缘下皮质(IL)和I组代谢型谷氨酸受体(mGluRs)在伤害性感受下行调制中的作用。在向大鼠IL内微量注射药物时,使用热诱导的爪部退缩来评估伤害性感受。对IL或相邻的前边缘皮质(PL)进行局部麻醉会促进伤害性感受,这表明IL和PL持续促进脊髓的抗伤害感受。用谷氨酸(GLU)进行相位激活揭示了PL和IL的相反作用;PL中的GLU具有快速的抗伤害感受作用,而在IL中它具有起效缓慢的促伤害感受作用。在ARTH动物和对照动物中,向IL给药局部麻醉药或GLU产生了相同的结果。在IL中给予mGluR5激动剂在两组中均诱导出促伤害感受作用,而mGluR5拮抗剂在对照动物中无作用,但在ARTH大鼠中诱导出抗伤害感受作用。激活IL中的mGluR1(通过共同给予mGluR1/5激动剂和mGluR5拮抗剂)在对照动物中未改变伤害性感受,但在ARTH动物中诱导出抗伤害感受作用。在两个实验组中,向IL给药mGluR1拮抗剂均未能改变伤害性感受。最后,mGluR5拮抗剂而非mGluR1拮抗剂阻断了两组中GLU的促伤害感受作用。结果表明,IL有助于伤害性感受的下行调制。IL中的mGluR5增强了健康对照动物和单关节炎动物的伤害性感受,在ARTH动物中这种作用是持续性的。此外,单关节炎发展后,激活IL中的mGluR1会减弱伤害性感受。

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