4.7 Article

Tetrahydrobiopterin modulates the behavioral neuroinflammatory response to an LPS challenge in mice

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 105, Issue -, Pages 139-148

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2022.06.016

Keywords

BH4; Dopamine; Inflammation; Depression

Funding

  1. Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Envirronnement (INRAe, France) (Departement AlimH)
  2. Marcel Dassault Prize for Research in Mental Disorders (Fondation FondaMental)
  3. Fondation pour la Recherche Medicale (FRM) [ENV202003011543]
  4. INRAe
  5. Universite de Bordeaux

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This study aimed to investigate the response of the brain BH4 pathway to inflammatory stimulus and found that BH4 supply can help maintain or restore dopaminergic neurotransmission under inflammatory conditions. Experimental results indicated that BH4 activity may decrease in inflammation, but BH4 supply can effectively increase BH4 levels, restore dopamine levels, and dampen inflammatory cytokine expression.
Tetrahydrobiopterin (BH4) is a necessary cofactor for the synthesis of monoamines from essential amino-acids, phenylalanine, tyrosine and tryptophan. The BH4 synthesis pathway is induced by inflammatory factors but highly regulated processes maintain levels in a physiological range. However, BH4 activity can be durably altered in inflammation-related pathologies, such as certain types of depression, potentially involving impair-ment of dopaminergic neurotransmission. The purpose of this study was to investigate the response of the brain BH4 pathway to the inflammatory stimulus induced by lipopolysaccharide (LPS) in mice. Brain expression of genes related to BH4 synthesis, levels of BH4, changes in L-aromatic amino acid precursors of monoamines and dopamine levels were determined. As secondary aim, the effect of acute BH4 supply under the inflammatory challenge was tested on these parameters and on the expression of inflammatory cytokines. Mice were also submitted to the sucrose preference test and to the open-field in order to asses hedonic and locomotor responses to LPS, in addition to their modulation by BH4 supply. The LPS challenge resulted in decreased striatal DA levels and increased Phenylalanine/Tyrosine ratio, suggesting reduced BH4 activity. BH4 supply was effective to in-crease striatal BH4 levels, to restore the LPS-induced decreased in DA levels in striatum and to dampen the LPS-induced expression of inflammatory cytokines. At the behavioral level, BH4 supply was able to restore the loss of locomotor response to amphetamine in the LPS treated mice, suggesting a modulation of the dopaminergic neurotransmission.These data suggest that BH4 can be considered as a potential add-on molecule, helping to maintain or restore dopaminergic neurotransmission in neuroinflammatory conditions..

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