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外侧下丘脑的食欲素 1 受体参与调节与大鼠偏头痛样状态相关的认知缺陷。

Orexin one receptors within the basolateral amygdala are involved in the modulation of cognitive deficits associated with a migraine-like state in rats.

机构信息

Department of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran.

Department of Biology, Faculty of Sciences, Lorestan University, Khorramabad, Iran.

出版信息

Neurol Res. 2021 Dec;43(12):1087-1097. doi: 10.1080/01616412.2021.1949687. Epub 2021 Jul 7.

Abstract

OBJECTIVES

This study explored the possible role of orexin one receptors (Orx1R) in the basolateral amygdala (BLA) on the modulation of nitroglycerin (NTG)-induced migraine-like symptoms. In addition, pain-induced subsequent alteration in learning and memory competence was evaluated in the adult male Wistar rats.

METHODS

The rats were given NTG (5 mg/kg, i.p.) every two days (for nine-day) to induce a migraine-like state. The migraine animals were treated with intra-BLA infusion of an Orx1R antagonist SB 334,867 (10, 20, and 40 nM/rat) or its vehicle DMSO. The NTG-induced migraine symptoms were recorded for 90 min. Spatial and passive avoidance performances were assessed by Morris water maze (MWM) and shuttle box tasks, respectively.

RESULTS

In comparison with control, NTG produced significant migraine-like symptoms characterized by a decrease in cage climbing and an increase in head-scratching, freezing, and facial grooming behavior. Intra-BLA infusion of SB 334,867 (40 nM/rat) significantly decreased cage climbing and increased facial grooming responses in NTG-treated rats. Moreover, all administrated doses of SB 334,867 increased NTG-evoked head-scratching and freezing behavior. Besides, NTG impaired learning and memory performances in both tests, which were exaggerated by post-injection of SB 334,867 (40 nM/rat).

CONCLUSIONS

Overall, the data provided an emerging for the within BLA in the modulation of cognitive decline comorbid with migraine in rats.

摘要

目的

本研究探讨了外侧下丘脑(BLA)中的食欲素 1 型受体(Orx1R)在调节硝化甘油(NTG)诱导的偏头痛样症状中的可能作用。此外,评估了成年雄性 Wistar 大鼠中疼痛引起的随后学习和记忆能力的改变。

方法

每隔两天给大鼠腹腔注射 NTG(5mg/kg,共九天)以诱导偏头痛样状态。用 BLA 内注射 Orx1R 拮抗剂 SB 334,867(10、20 和 40 nM/大鼠)或其载体 DMSO 治疗偏头痛动物。记录 NTG 诱导的偏头痛症状 90 分钟。通过 Morris 水迷宫(MWM)和穿梭箱任务分别评估空间和被动回避表现。

结果

与对照组相比,NTG 产生了显著的偏头痛样症状,表现为笼内攀爬减少,头抓挠、冻结和面部梳理行为增加。BLA 内注射 SB 334,867(40 nM/大鼠)可显著减少 NTG 治疗大鼠的笼内攀爬,并增加面部梳理反应。此外,SB 334,867 的所有给药剂量均增加了 NTG 诱发的头抓挠和冻结行为。此外,NTG 损害了两种测试中的学习和记忆表现,而 SB 334,867(40 nM/大鼠)的注射后加剧了这种损害。

结论

总体而言,这些数据为 BLA 内的 Orx1R 在调节偏头痛合并认知下降提供了新的见解。

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