4.6 Article

Higher Levels of Pro-inflammatory Cytokines Are Associated With Higher Levels of Glutamate in the Anterior Cingulate Cortex in Depressed Adolescents

期刊

FRONTIERS IN PSYCHIATRY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2021.642976

关键词

glutamate; depression; magnetic resonance spectroscopy; interleukin-6; ascorbate

资金

  1. National Institutes of Health [K01MH117442, R37MH101495]
  2. Klingenstein Third Generation Foundation (Child and Adolescent Depression Fellow Award)
  3. Stanford Maternal Child and Health Institute
  4. Stanford Center for Cognitive and Neurobiological Imaging Center
  5. Ray and Dagmar Dolby Family Fund

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This study found that peripheral inflammation in adolescents with depression can affect glutamate levels in the brain, and antioxidants like ascorbate may help mitigate the impact of inflammation on glutamate metabolism. The results underscore the importance of considering both immune and neural factors in studying depression, and highlight the potential role of anti-inflammatory compounds in alleviating the adverse effects of inflammation.
Animal models of stress and related conditions, including depression, have shown that elevated peripheral levels of inflammatory cytokines have downstream consequences on glutamate (Glu) in the brain. Although studies in human adults with depression have reported evidence of higher inflammation but lower Glu in the anterior cingulate cortex (ACC), the extent to which peripheral inflammation contributes to glutamatergic abnormalities in adolescents with depression is not well-understood. It is also unclear whether antioxidants, such as ascorbate (Asc), may buffer against the effects of inflammation on Glu metabolism. Fifty-five depressed adolescents were recruited in the present cross-sectional study and provided blood samples, from which we assayed pro-inflammatory cytokines, and underwent a short-TE proton magnetic spectroscopy scan at 3T, from which we estimated Glu and Asc in the dorsal ACC. In the 31 adolescents with usable cytokine and Glu data, we found that IL-6 was significantly positively associated with dorsal ACC Glu (beta = 0.466 +/- 0.199, p = 0.029). Of the 16 participants who had usable Asc data, we found that at higher levels of dorsal ACC Asc, there was a negative association between IL-6 and Glu (interaction effect: beta = -0.906 +/- 0.433, p = 0.034). Importantly, these results remained significant when controlling for age, gender, percentage of gray matter in the dorsal ACC voxel, BMI, and medication (antidepressant and anti-inflammatory) usage. While preliminary, our results underscore the importance of examining both immune and neural contributors to depression and highlight the potential role of anti-inflammatory compounds in mitigating the adverse effects of inflammation (e.g., glutamatergic neuroexcitotoxicity). Future studies that experimentally manipulate levels of inflammation, and of ascorbate, and that characterize these effects on cortical glutamate concentrations and subsequent behavior in animals and in humans are needed.

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