Hosaini Mojtaba, Abbasnejad Mehdi, Kooshki Razieh, Esmaeili-Mahani Saeed, Raoof Maryam, Naderi Reyhaneh, Aarab Ghizlane, Lobbezoo Frank
Department of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran.
Department of Biology, Faculty of Sciences, Lorestan University, Khorramabad, Iran.
Odontology. 2025 Apr;113(2):764-775. doi: 10.1007/s10266-024-01021-0. Epub 2025 Jan 23.
Orexin-A (OXA), a neuropeptide produced in the hypothalamus, is recognized for its role in modulating orofacial nociception and regulating feeding behaviors, as well as its impact on psychophysiological responses. This study investigated the role of orexin-1 receptors (OX1R) in modulating nociceptive behaviors induced by noxious stimulation of the temporomandibular joint (TMJ) and the associated changes in mood and feeding behaviors in rats with complete Freund's adjuvant (CFA)-induced temporomandibular disorders (TMDs). Bilateral cannulation of the lateral ventricles was performed in rats. To induce nociception, CFA was injected unilaterally into the left TMJ of the rats. Nociceptive behaviors were assessed using the hot plate and tail flick tests, while anxiety-like behavior and food intake were evaluated using an elevated plus maze (EPM) and a food preference device, respectively. The results demonstrated a significant increase in nociceptive scores and anxiety-like behaviors, along with reductions in water and food consumption following CFA injection. However, post-treatment with OXA at concentrations of 50 and 100 pM/rat significantly decreased thermal nociceptive scores, alleviated anxiety-like behavior, and increased water and food intake. These beneficial effects were reversed when OXA was co-administered with SB-334867 (40 nM/rat), an OX1R antagonist. Collectively, our findings suggest that OX1R signaling plays a role in the modulation of anxiety-like behavior and abnormalities in food intake in CFA-treated rats. Understanding the involvement of OXA and its receptors in CFA-induced TMJ nociception and behavioral changes may pave the way for potential therapeutic interventions targeting OX1R signaling in the management of TMD-associated symptoms.
食欲素A(OXA)是一种在下丘脑中产生的神经肽,因其在调节口腔面部伤害感受、调节进食行为以及对心理生理反应的影响而被人们所认识。本研究调查了食欲素-1受体(OX1R)在调节由颞下颌关节(TMJ)有害刺激诱导的伤害感受行为以及在完全弗氏佐剂(CFA)诱导的颞下颌关节紊乱(TMD)大鼠中相关的情绪和进食行为变化方面的作用。对大鼠进行双侧侧脑室插管。为了诱导伤害感受,将CFA单侧注射到大鼠的左TMJ中。使用热板法和甩尾试验评估伤害感受行为,同时分别使用高架十字迷宫(EPM)和食物偏好装置评估焦虑样行为和食物摄入量。结果表明,注射CFA后,伤害感受评分和焦虑样行为显著增加,同时水和食物消耗量减少。然而,以50和100 pM/大鼠的浓度用OXA进行治疗后,热伤害感受评分显著降低,焦虑样行为得到缓解,水和食物摄入量增加。当OXA与OX1R拮抗剂SB-334867(40 nM/大鼠)共同给药时,这些有益作用被逆转。总的来说,我们的研究结果表明,OX1R信号传导在CFA处理的大鼠中焦虑样行为的调节和食物摄入异常中发挥作用。了解OXA及其受体在CFA诱导的TMJ伤害感受和行为变化中的作用,可能为在TMD相关症状管理中针对OX1R信号传导的潜在治疗干预铺平道路。