Cano-Barquilla Pilar, Jiménez-Ortega Vanesa, Fernández-Mateos Pilar, Virto Leire, Maldonado Bautista Estela, Perez-Miguelsanz Juliana, Esquifino Ana I
Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28003 Madrid, Spain.
Int J Mol Sci. 2025 Jan 11;26(2):577. doi: 10.3390/ijms26020577.
Melatonin is involved in various functions such as the timing of circadian rhythms, energy metabolism, and body mass gain in experimental animals. However, its effects on adipose tissue lipid metabolism are still unclear. This study analyzes the effects of melatonin on the relative gene expression of lipolytic proteins in rat mesenteric adipose tissue and free fatty acid (FFA) and glycerol plasma levels of male Wistar rats fed a high-fat (HFD) or maintenance diet. Four experimental groups were established: control, obese, and control or obese plus 2.3 mg/kg/day of melatonin in tap water. After 11 weeks, animals were sacrificed at different times throughout a 24 h cycle, and mesenteric adipose tissue and plasma samples were collected and analyzed. , , and gene expression, as well as FFA and glycerol concentrations, showed rhythm patterns in the control group. HFD disrupted those rhythm patterns and increased FFA and glycerol concentrations during the dark photoperiod. In both melatonin-treated groups, almost all analyzed genes showed circadian patterns. Notably, melatonin significantly prevented the increase in FFA levels during the dark photoperiod in obese rats (obese group: ~1100 mM vs. obese + melatonin group: ~600 μM, similar to control levels). However, the rhythmic pattern observed in control animals was not sustained. According to our results, melatonin could regulate circadian gene transcription of mesenteric adipose tissue lipolysis proteins. The effect of melatonin on preventing elevated FFA plasma levels associated with high-fat diet intake warrants further investigation.
褪黑素参与多种功能,如实验动物的昼夜节律调节、能量代谢和体重增加。然而,其对脂肪组织脂质代谢的影响仍不清楚。本研究分析了褪黑素对高脂(HFD)或维持饮食喂养的雄性Wistar大鼠肠系膜脂肪组织中脂解蛋白相对基因表达以及游离脂肪酸(FFA)和甘油血浆水平的影响。建立了四个实验组:对照组、肥胖组,以及对照组或肥胖组加2.3毫克/千克/天的褪黑素(溶于自来水中)。11周后,在24小时周期内的不同时间点处死动物,并收集和分析肠系膜脂肪组织和血浆样本。对照组中, 、 和 基因表达以及FFA和甘油浓度呈现节律模式。高脂饮食扰乱了这些节律模式,并在暗期增加了FFA和甘油浓度。在两个褪黑素处理组中,几乎所有分析的基因都呈现昼夜节律模式。值得注意的是,褪黑素显著阻止了肥胖大鼠在暗期FFA水平的升高(肥胖组:约1100微摩尔/升 vs. 肥胖 + 褪黑素组:约600微摩尔/升,与对照组水平相似)。然而,在对照动物中观察到的节律模式并未持续。根据我们的结果,褪黑素可能调节肠系膜脂肪组织脂解蛋白的昼夜基因转录。褪黑素对预防与高脂饮食摄入相关的血浆FFA水平升高的作用值得进一步研究。