Ilavská Lucia, Morvová Marcela, Paduchová Zuzana, Muchová Jana, Garaiova Iveta, Ďuračková Zdenka, Šikurová Libuša, Trebatická Jana
Department of Nuclear Physics and Biophysics, Faculty of Mathematics, Physics and Informatics, Comenius University, Bratislava, Slovakia.
Institute of Medical Chemistry, Biochemistry and Clinical Biochemistry, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Front Psychiatry. 2024 Feb 13;15:1347178. doi: 10.3389/fpsyt.2024.1347178. eCollection 2024.
Depressive disorder is a severe mental condition. In addition to genetic factors, immunological-inflammatory factors, oxidative stress, and disturbances in neurotransmitter metabolism, kynurenine and serotonin pathways may play a role. The exact mechanisms, especially in depressed children and adolescents, are not fully understood. Our primary hypothesis was whether the metabolites of tryptophan degradation in children and adolescents with depressive disorder might be influenced by omega-3 FAs compared to omega-6 FAs during a 12-week supplementation. A secondary hypothesis was to investigate whether tryptophan metabolites in children and adolescents are associated with markers of inflammatory response, oxidative stress, cortisol, and the serum omega-6/omega-3 FA ratio. Metabolites of tryptophan degradation and pteridines, neopterin, and biopterin in urine were analyzed with an HPLC system. Surprisingly, omega-3 FAs stimulated both kynurenine (kynurenine/tryptophan ratio) and serotonin (5-hydroxytryptophan) pathways, whereas omega-6 FAs only increased the kynurenine/tryptophan ratio. Neopterin and biopterin were not different from the healthy controls. Biopterin increased after omega-3 FA supplementation. Serotonin was positively correlated with lipoperoxidation and a marker of oxidative protein damage. Of the monitored tryptophan metabolites, only 5-hydroxyindolacetic acid was positively correlated with the severity of depression, total cholesterol, and negatively with brain-derived neurotrophic factor and glutathione peroxidase. In conclusion, in children and adolescents, both supplemented FAs stimulated the kynurenine pathway (kynurenine/tryptophan ratio) and kynurenine formation. However, the serotonin pathway (5-hydroxytryptophan) was stimulated only by omega-3 FA. Tryptophan metabolism is associated with oxidative stress, inflammation, total cholesterol, and cortisol. We are the first to point out the association between the kynurenine pathway (KYN/TRP ratio) and the omega-6/omega-3 FA ratio. The metabolite 5-HIAA could play a role in the pathophysiology of depressive disorder in children and adolescents.
https://www.isrctn.com/ISRCTN81655012, identifier ISRCTN81655012.
抑郁症是一种严重的精神疾病。除了遗传因素、免疫炎症因素、氧化应激和神经递质代谢紊乱外,犬尿氨酸和血清素途径可能也起作用。确切机制,尤其是在抑郁的儿童和青少年中,尚未完全了解。我们的主要假设是,与ω-6脂肪酸相比,在12周的补充期内,ω-3脂肪酸是否可能影响患有抑郁症的儿童和青少年中色氨酸降解的代谢产物。次要假设是研究儿童和青少年中的色氨酸代谢产物是否与炎症反应、氧化应激、皮质醇的标志物以及血清ω-6/ω-3脂肪酸比值相关。用高效液相色谱系统分析尿液中色氨酸降解的代谢产物以及蝶啶、新蝶呤和生物蝶呤。令人惊讶的是,ω-3脂肪酸刺激了犬尿氨酸(犬尿氨酸/色氨酸比值)和血清素(5-羟色氨酸)途径,而ω-6脂肪酸仅增加了犬尿氨酸/色氨酸比值。新蝶呤和生物蝶呤与健康对照组无差异。补充ω-3脂肪酸后生物蝶呤增加。血清素与脂质过氧化和氧化蛋白质损伤的标志物呈正相关。在所监测的色氨酸代谢产物中,只有5-羟吲哚乙酸与抑郁症严重程度、总胆固醇呈正相关,与脑源性神经营养因子和谷胱甘肽过氧化物酶呈负相关。总之,在儿童和青少年中,两种补充的脂肪酸都刺激了犬尿氨酸途径(犬尿氨酸/色氨酸比值)和犬尿氨酸的形成。然而,血清素途径(5-羟色氨酸)仅受ω-3脂肪酸刺激。色氨酸代谢与氧化应激、炎症、总胆固醇和皮质醇相关。我们是第一个指出犬尿氨酸途径(KYN/TRP比值)与ω-6/ω-3脂肪酸比值之间关联的。代谢产物5-HIAA可能在儿童和青少年抑郁症的病理生理学中起作用。