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Modulatory role of hippocampal dopamine receptors in antinociceptive responses induced by chemical stimulation of the lateral hypothalamus in an animal model of persistent inflammatory pain.
Brain Research Bulletin ( IF 3.5 ) Pub Date : 2020-06-30 , DOI: 10.1016/j.brainresbull.2020.06.017
Masoud Zakeri 1 , Saeed Soltanizadeh 1 , Saeideh Karimi-Haghighi 2 , Abbas Haghparast 2
Affiliation  

The lateral hypothalamus (LH) plays a complicated role in the modulation of inflammatory pain. There are a number of connections between the LH and the hippocampus. This study evaluated the pain modulatory role of intra-CA1 dopamine receptors in LH chemical stimulation-induced antinociception in the formalin test (persistent inflammatory pain model). Vehicle control groups received saline or DMSO into the CA1 and saline into the LH. Carbachol control groups received carbachol (250 nM) into the LH 5 min after saline or DMSO injections into the CA1. In the treatment groups, intra-CA1 administration of SCH-23,390 or Sulpiride (D1- or D2-like dopamine receptor antagonists, respectively) was performed 5 min before carbachol injection. Formalin tests were done in all rats 5 min after the second injection. LH chemical stimulation-induced antinociception during both phases of the formalin test was alleviated by the intra-CA1 administration of dopamine receptor antagonists. The inhibitory effects of the D1 or D2-like dopamine receptor antagonist on LH chemical stimulation-induced analgesia was nearly the same in the both phases of formalin‐induced pain-related behaviors. The findings show that the LH-CA1 pathway contributes to the modulation of formalin-induced pain. Moreover, the results indicate that D1- and D2-like dopamine receptors in the CA1 participate in the LH chemical stimulation-induced antinociception.



中文翻译:

海马多巴胺受体在持续炎症性疼痛动物模型中下丘脑外侧化学刺激诱导的镇痛反应中的调节作用。

外侧下丘脑 (LH) 在炎症性疼痛的调节中起着复杂的作用。LH 和海马体之间有许多联系。本研究在福尔马林试验(持续炎症性疼痛模型)中评估了 CA1 内多巴胺受体在 LH 化学刺激诱导的镇痛作用中的疼痛调节作用。媒介物对照组接受生理盐水或DMSO进入CA1,生理盐水进入LH。在将盐水或 DMSO 注射到 CA1 后 5 分钟,卡巴胆碱对照组接受到 LH 中的卡巴胆碱 (250 nM)。在治疗组中,在卡巴胆碱注射前 5 分钟进行 SCH-23,390 或舒必利(分别为 D1 或 D2 样多巴胺受体拮抗剂)的 CA1 内给药。在第二次注射后 5 分钟对所有大鼠进行福尔马林试验。在福尔马林试验的两个阶段中,LH 化学刺激诱导的镇痛作用通过多巴胺受体拮抗剂的 CA1 内给药得到缓解。D1 或 D2 样多巴胺受体拮抗剂对 LH 化学刺激诱导的镇痛的抑制作用在福尔马林诱导的疼痛相关行为的两个阶段几乎相同。研究结果表明,LH-CA1 通路有助于调节福尔马林引起的疼痛。此外,结果表明 CA1 中的 D1 和 D2 样多巴胺受体参与 LH 化学刺激诱导的镇痛作用。D1 或 D2 样多巴胺受体拮抗剂对 LH 化学刺激诱导的镇痛的抑制作用在福尔马林诱导的疼痛相关行为的两个阶段几乎相同。研究结果表明,LH-CA1 通路有助于调节福尔马林引起的疼痛。此外,结果表明 CA1 中的 D1 和 D2 样多巴胺受体参与 LH 化学刺激诱导的镇痛作用。D1 或 D2 样多巴胺受体拮抗剂对 LH 化学刺激诱导的镇痛的抑制作用在福尔马林诱导的疼痛相关行为的两个阶段几乎相同。研究结果表明,LH-CA1 通路有助于调节福尔马林引起的疼痛。此外,结果表明 CA1 中的 D1 和 D2 样多巴胺受体参与 LH 化学刺激诱导的镇痛作用。

更新日期:2020-07-05
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