Malaei Beriwan, Farajdokht Fereshteh, Mohaddes Gisou, Mansouri Behzad, Hamidi Nasrin, Alipour Mohammad Reza
Neurosciences Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Physiology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
J Cell Mol Med. 2025 Aug;29(15):e70770. doi: 10.1111/jcmm.70770.
The contemporary lifestyle has resulted in an epidemic of chronic sleep restriction (SR), which has emerged as a substantial contributor to mood disorders, particularly anxiety and depression. This study examined the effectiveness of AdipoRon (Adipo), a synthetic adiponectin agonist, in mitigating anxious behaviours and depression-like symptoms in a chronic SR mice model. Forty male Swiss albino mice were divided into four groups: wide platform (WP), SR, SR + melatonin (Mel), and SR + Adipo. Over 21 days, the animals underwent a modified multiple-platform technique to induce SR, followed by daily intranasal treatments. The open field test and elevated plus maze were conducted to assess anxiety-related behaviours, while the forced swimming test and sucrose splash test were used to assess depressive symptoms. Serum corticosterone concentrations, a marker of microglia activation, and pro-inflammatory mediators (NF-кB and IL-1β) in the prefrontal cortex (PFC) were also examined. Intranasal administration of Adipo markedly decreased anxiety-like behaviours, despair, and apathy in sleep-restricted mice compared to the SR group. Adipo therapy also reduced pro-inflammatory proteins and ionised calcium-binding adaptor molecule-1 (Iba-1)-positive cells in the PFC and restored serum corticosterone levels. These outcomes emphasise the therapeutic benefit of Adipo as an alternative therapy for mood disorders associated with SR.
当代生活方式导致了慢性睡眠限制(SR)的流行,而慢性睡眠限制已成为情绪障碍,尤其是焦虑和抑郁的重要促成因素。本研究考察了合成脂联素激动剂AdipoRon(Adipo)在缓解慢性SR小鼠模型中的焦虑行为和抑郁样症状方面的有效性。将40只雄性瑞士白化小鼠分为四组:宽平台组(WP)、SR组、SR + 褪黑素(Mel)组和SR + Adipo组。在21天的时间里,动物们接受改良的多平台技术诱导SR,随后进行每日鼻内给药治疗。通过旷场试验和高架十字迷宫评估焦虑相关行为,同时使用强迫游泳试验和蔗糖偏好试验评估抑郁症状。还检测了血清皮质酮浓度(小胶质细胞激活的标志物)以及前额叶皮质(PFC)中的促炎介质(NF-κB和IL-1β)。与SR组相比,鼻内给予Adipo可显著降低睡眠受限小鼠的焦虑样行为、绝望和冷漠。Adipo治疗还降低了PFC中的促炎蛋白和离子钙结合衔接分子1(Iba-1)阳性细胞,并恢复了血清皮质酮水平。这些结果强调了Adipo作为与SR相关情绪障碍替代疗法的治疗益处。