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内侧视前区核内给予过氧化物酶体增殖物激活受体拮抗剂对福尔马林诱发的痛觉行为、条件性镇痛、以及有或无伤害性感受音存在时条件性恐惧的影响。

Effects of Intra-BLA Administration of PPAR Antagonists on Formalin-Evoked Nociceptive Behaviour, Fear-Conditioned Analgesia, and Conditioned Fear in the Presence or Absence of Nociceptive Tone in Rats.

机构信息

Pharmacology and Therapeutics, National University of Ireland Galway, H91 W5P7 Galway, Ireland.

Galway Neuroscience Centre, National University of Ireland Galway, H91 W5P7 Galway, Ireland.

出版信息

Molecules. 2022 Mar 21;27(6):2021. doi: 10.3390/molecules27062021.

DOI:10.3390/molecules27062021
PMID:35335382
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8949000/
Abstract

There is evidence for the involvement of peroxisome proliferator-activated receptors (PPARs) in pain, cognition, and anxiety. However, their role in pain-fear interactions is unknown. The amygdala plays a key role in pain, conditioned fear, and fear-conditioned analgesia (FCA). We investigated the effects of intra-basolateral amygdala (BLA) administration of PPARα, PPARβ/δ, and PPARγ antagonists on nociceptive behaviour, FCA, and conditioned fear in the presence or absence of nociceptive tone. Male Sprague-Dawley (SD) rats received footshock (FC) or no footshock (NFC) in a conditioning arena. Twenty-three and a half hours later, rats received an intraplantar injection of formalin or saline and, 15 min later, intra-BLA microinjections of vehicle, PPARα (GW6471) PPARβ/δ (GSK0660), or PPARγ (GW9662) antagonists before arena re-exposure. Pain and fear-related behaviour were assessed, and neurotransmitters/endocannabinoids measured post-mortem. Intra-BLA administration of PPARα or PPARγ antagonists potentiated freezing in the presence of nociceptive tone. Blockade of all PPAR subtypes in the BLA increased freezing and BLA dopamine levels in NFC rats in the absence of nociceptive tone. Administration of intra-BLA PPARα and PPARγ antagonists increased levels of dopamine in the BLA compared with the vehicle-treated counterparts. In conclusion, PPARα and PPARγ in the BLA play a role in the expression or extinction of conditioned fear in the presence or absence of nociceptive tone.

摘要

有证据表明过氧化物酶体增殖物激活受体 (PPARs) 参与疼痛、认知和焦虑。然而,它们在疼痛-恐惧相互作用中的作用尚不清楚。杏仁核在疼痛、条件性恐惧和恐惧条件性镇痛 (FCA) 中发挥关键作用。我们研究了内侧基底杏仁核 (BLA) 中 PPARα、PPARβ/δ 和 PPARγ 拮抗剂的给药对内源性痛觉、FCA 和存在或不存在痛觉音时条件性恐惧的影响。雄性 Sprague-Dawley (SD) 大鼠在条件性竞技场中接受足部电击 (FC) 或不接受足部电击 (NFC)。23 个半小时后,大鼠接受足底注射福尔马林或生理盐水,15 分钟后,在重新暴露于竞技场之前,进行内侧基底杏仁核内微注射载体、PPARα (GW6471)、PPARβ/δ (GSK0660) 或 PPARγ (GW9662) 拮抗剂。评估疼痛和与恐惧相关的行为,并在死后测量神经递质/内源性大麻素。内侧基底杏仁核内给予 PPARα 或 PPARγ 拮抗剂可增强痛觉音存在时的冻结反应。BLA 中所有 PPAR 亚型的阻断增加了 NFC 大鼠中无痛觉音时的冻结和 BLA 多巴胺水平。与载体处理的对应物相比,内侧基底杏仁核内给予 PPARα 和 PPARγ 拮抗剂可增加 BLA 中的多巴胺水平。总之,BLA 中的 PPARα 和 PPARγ 在存在或不存在痛觉音的情况下,在条件性恐惧的表达或消退中发挥作用。

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