Journal
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY
Volume 395, Issue 10, Pages 1269-1282Publisher
SPRINGER
DOI: 10.1007/s00210-022-02274-8
Keywords
Streptozotocin; Elevated plus maze; Forced swimming test; Specialized pro-resolving lipid mediators; Anxiety; Depression
Categories
Funding
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [303863/2020-0, 307186/2017-2]
- Programa de Apoio a Grupos de Excelencia (PRONEX)
- SETI/Fundacao Araucaria
- MCTI/CNPq
- Governo do Estado do Parana [014/2017, 46.843]
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The study found that a specialized pro-resolving lipid mediator called Resolvin D5 (RvD5) can prevent depression and anxiety symptoms associated with Type 1 diabetes mellitus (T1DM) and significantly improve blood glucose levels. Furthermore, RvD5 also reduces inflammation in the hippocampus and prefrontal cortex of experimental-T1DM rats. These findings suggest that RvD5 has potential preventive and therapeutic effects on emotional complications resulting from T1DM, possibly through its action on neuroinflammation.
Type 1 diabetes mellitus (T1DM) is a chronic disease related to a persistent inflammatory process reaching the central nervous system, which leads to psychiatric comorbidities such as depression and anxiety. The search for new therapeutic agents effective in alleviating the psychiatric condition associated with T1DM becomes critical. Using an animal model of T1DM, we aimed to evaluate the effect of a specific specialized pro-resolving lipid mediator Resolvin D5 (RvD5), in preventing behaviors related to depression and anxiety, investigating its influence on inflammasome in interleukin (IL)-1 beta in the hippocampus and prefrontal cortex. After experimental T1DM induction with streptozotocin (60 mg/kg, i.p.), these animals were treated for 23 days and randomly divided into 6 subgroups according to the treatment: vehicle (VEH), the antidepressant Fluoxetine (FLX; 10 mg/kg), the nonsteroidal anti-inflammatory Ibuprofen (IBU; 30 mg/kg) or Resolvin D5 (RvD5; 1 3, or 10 ng/animal). As a control group for the experimental-T1DM condition, a group of normoglycemic animals treated with VEH underwent the same behavioral tests: elevated plus maze, open field, and modified forced swimming tests. In the end, hippocampus and prefrontal cortex samples were processed to analyze the pro-inflammatory cytokine IL-1 beta levels. Our data showed that RvD5 treatment prevented the more pronounced anxious-like and reduced the depressive-like behaviors of experimental-T1DM animals and significantly improved the plasma glucose levels. Additionally, RvD5 treatment prevented the increased level of pro-inflammatory cytokine IL-1 beta in the hippocampus and prefrontal cortex of experimental-T1DM rats. To conclude, RvD5 presents a preventive therapeutic potential in impairing the development of the emotional complications resulting from T1DM. This potential may be related to its protective profile, as demonstrated in this study by its pro-resolutive action on neuroinflammation in the hippocampus and prefrontal cortex.
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