Omega-3 alleviates behavioral and molecular changes in a mouse model of stress-induced juvenile depression

被引:2
|
作者
Strekalova, Tatyana [1 ,2 ]
-Smith, Daniel Radford [2 ]
Dunstan, Isobel K. [2 ]
Gorlova, Anna [3 ]
Svirin, Evgeniy
Sheveleva, Elisaveta [3 ,5 ]
Burova, Alisa [3 ]
Morozov, Sergey [3 ]
Lyundup, Aleksey [4 ,6 ]
Berger, Gregor [7 ]
Anthony, Daniel C. [2 ]
Walitza, Susanne [7 ]
机构
[1] Maastricht Univ, Dept Psychiat & Neuropsychol, Univ Singel 40, NL-6229 ER Maastricht, Netherlands
[2] Univ Oxford, Dept Pharmacol, Mansfield Rd, Oxford OX1 3QT, England
[3] Inst Gen Pathol & Pathophysiol, Lab Cognit Dysfunct, Moscow, Russia
[4] RUDN Univ, 6 Miklukho Maklaya Str, Moscow, Russia
[5] Sechenov Moscow State Med Univ, Dept Normal Physiol, Moscow, Russia
[6] Endocrinol Res Ctr, Dmitry Ulyanov Str 19, Moscow 117036, Russia
[7] Univ Zuerich, Dept Child & Adolescent Psychiat & Psychotherapy, Zurich, Switzerland
来源
NEUROBIOLOGY OF STRESS | 2024年 / 31卷
关键词
Juvenile depression; Omega-3; Eicosapentaenoic and docosahexaenoic acids; Ultrasound stress; Metabolome; Mice; INFLAMMATORY RESPONSE; PSYCHIATRIC-DISORDERS; LIPID MEDIATORS; CHILDREN; ADOLESCENT; MICE; ANXIETY; EXPRESSION; DEFICITS; PLACEBO;
D O I
10.1016/j.ynstr.2024.100646
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction: Depression is increasingly diagnosed in adolescence, necessitating specific prevention and treatment methods. However, there is a lack of animal models mimicking juvenile depression. This study explores a novel model using ultrasound (US) stress in juvenile mice. Methods: We employed the US stress model in one -month -old C57/BL6 mice, exposing them to alternating ultrasound frequencies (20 -25 kHz and 25 -45 kHz) for three weeks. These frequencies correspond to negative and neutral emotional states in rodents and can induce a depressive -like syndrome. Concurrently, mice received either an omega -3 food supplement (FS) containing eicosapentaenoic acid (EPA; 0.55 mg/kg/day) and docosahexaenoic acid (DHA; 0.55 mg/kg/day) or a vehicle. Post -stress, we evaluated anxiety- and depressive -like behaviors, blood corticosterone levels, brain expression of pro -inflammatory cytokines, and conducted metabolome analysis of brain, liver and blood plasma. Results: US -exposed mice treated with vehicle exhibited decreased sucrose preference, a sign of anhedonia, a key feature of depression, increased anxiety -like behavior, elevated corticosterone levels, and enhanced TNF and IL1 beta gene expression in the brain. In contrast, US -FS mice did not display these changes. Omega -3 supplementation also reduced anxiety -like behavior in non -stressed mice. Metabolomic analysis revealed US -induced changes in brain energy metabolism, with FS increasing brain sphingomyelin. Liver metabolism was affected by both US and FS, while plasma metabolome changes were exclusive to FS. Brain glucose levels correlated positively with activity in anxiety tests. Conclusion: Chronic omega -3 intake counteracted depressive- and anxiety -like behaviors in a US model of juvenile depression in mice. These effects likely stem from the anti-inflammatory properties of the supplement, suggesting potential therapeutic applications in juvenile depression.
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页数:14
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