Korkmaz Engin, Erden Yavuz, Tekin Çiğdem, Tekin Suat
Faculty of Medicine, Department of Physiology, İnönü University, Malatya, Türkiye.
Faculty of Science, Department of Molecular Biology and Genetics, Bartın University, Bartın, Türkiye.
Exp Physiol. 2025 Aug 13. doi: 10.1113/EP092783.
The hypothalamic nuclei play a central role in the synthesis of anorexigenic and orexigenic neuropeptides, which are regulated by peripheral hormones, like leptin and ghrelin. Melatonergic receptors (MT/MT) are prominently expressed in the arcuate nucleus of the hypothalamus - an essential hub for appetite control - and in peripheral metabolic tissues where leptin and ghrelin are secreted. Agomelatine, an antidepressant drug and potent MT/MT agonist, offers potential for modulating appetite. This study aimed to investigate the impact of agomelatine on appetite regulation. Forty male Sprague-Dawley rats were randomly allocated into four groups, control (no treatment), vehicle control, agomelatine 20 mg/kg (Ago-20), and agomelatine 40 mg/kg (Ago-40), and administered oral gavage for 14 days. Body weight and food intake were recorded daily. At the end of the experiment, rats were euthanized and blood and hypothalamic tissue samples were obtained. Agomelatine significantly reduced body weight (Ago-40: 275.2 ± 7.2 g vs. control: 339.7 ± 8.3 g, P < 0.05) and food intake (Ago-40: 20.21 ± 1.32 g vs. control: 32.09 ± 1.58 g, P < 0.05) by day 14, without affecting water intake. Plasma ghrelin levels decreased (Ago-40: 22.54 ± 3.95 ng/dL vs. control: 46.67 ± 4.84 ng/dL, P < 0.05), while leptin increased (Ago-40: 552.30 ± 41.67 pg/mL vs. control: 271.10 ± 32.12 pg/mL P < 0.05). Hypothalamic orexigenic neuropeptides neuropeptide Y (NPY) and agouti-related peptide (AgRP) were suppressed (NPY, Ago40: 0.61 ± 0.02 vs. Control: 1.36 ± 0.1321; AgRP, Ago40: 0.52 ± 0.03 vs. Control: 1.49 ± 0.27, P < 0.05), while anorexigenic cocaine- and amphetamine-regulated transcript (CART) and proopiomelanocortin (POMC) were elevated (CART: Ago40: 1.19 ± 0.08 vs. Control: 0.92 ± 0.06; POMC: Ago40: 1.49 ± 0.17 vs. Control: 0.67 ± 0.10, P < 0.05). These findings suggest agomelatine promotes weight loss by modulating appetite-related hormones and hypothalamic neuropeptides, highlighting its potential as a therapeutic for obesity and metabolic disorders.
下丘脑核在合成食欲抑制性和食欲刺激性神经肽方面发挥着核心作用,这些神经肽受外周激素如瘦素和胃饥饿素的调节。褪黑素能受体(MT/MT)在下丘脑弓状核(食欲控制的关键枢纽)以及分泌瘦素和胃饥饿素的外周代谢组织中显著表达。阿戈美拉汀是一种抗抑郁药物,也是强效的MT/MT激动剂,具有调节食欲的潜力。本研究旨在探讨阿戈美拉汀对食欲调节的影响。将40只雄性Sprague-Dawley大鼠随机分为四组:对照组(未治疗)、溶剂对照组、阿戈美拉汀20mg/kg组(Ago-20)和阿戈美拉汀40mg/kg组(Ago-40),通过口服灌胃给药14天。每天记录体重和食物摄入量。实验结束时,对大鼠实施安乐死,并采集血液和下丘脑组织样本。到第14天时,阿戈美拉汀显著降低了体重(Ago-40组:275.2±7.2g,对照组:339.7±8.3g,P<0.05)和食物摄入量(Ago-40组:20.21±1.32g,对照组:32.09±1.58g,P<0.05),但不影响水的摄入量。血浆胃饥饿素水平降低(Ago-40组:22.54±3.95ng/dL,对照组:46.67±4.84ng/dL,P<0.05),而瘦素水平升高(Ago-40组:552.30±41.67pg/mL,对照组:271.10±32.12pg/mL,P<0.05)。下丘脑食欲刺激性神经肽神经肽Y(NPY)和刺鼠相关肽(AgRP)受到抑制(NPY,Ago40组:0.61±0.02,对照组:1.36±0.1321;AgRP,Ago40组:0.52±0.03,对照组:1.49±0.27,P<0.05),而食欲抑制性的可卡因和苯丙胺调节转录物(CART)和阿黑皮素原(POMC)则升高(CART:Ago40组:1.19±0.08,对照组:0.92±0.06;POMC:Ago40组:1.49±0.17,对照组:0.67±0.10,P<0.05)。这些发现表明,阿戈美拉汀通过调节与食欲相关的激素和下丘脑神经肽来促进体重减轻,凸显了其作为肥胖症和代谢紊乱治疗药物的潜力。