4.8 Article

Anti-inflammatory mechanisms and pharmacological actions of phycocyanobilin in a mouse model of experimental autoimmune encephalomyelitis: A therapeutic promise for multiple sclerosis

Journal

FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.1036200

Keywords

interferon-beta; proinflammatory cytokines; remyelination; antioxidants; experimental autoimmune encephalomyelitis; multiple sclerosis; phycocyanobilin

Categories

Funding

  1. Federal Ministry of Education and Research of Germany (BMBF)
  2. Science without Borders Program of Brazil
  3. [01DN18042]
  4. [405878/2013-3]

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In this study, the potential benefits and mechanisms of action of Phycocyanobilin (PCB) in combating chronic experimental autoimmune encephalomyelitis (EAE), a nonclinical model of multiple sclerosis (MS), were evaluated. The study found that PCB can improve neurological symptoms, reduce inflammatory cytokine levels, and regulate relevant genes at the genetic level. In addition, PCB can reduce demyelination, decrease neuronal damage, and promote the generation of oligodendrocyte precursor cells. The combination of PCB with Interferon-beta (IFN-beta) showed better therapeutic effects.
Cytokines, demyelination and neuroaxonal degeneration in the central nervous system are pivotal elements implicated in the pathogenesis of multiple sclerosis (MS) and its nonclinical model of experimental autoimmune encephalomyelitis (EAE). Phycocyanobilin (PCB), a chromophore of the biliprotein C-Phycocyanin (C-PC) from Spirulina platensis, has antioxidant, immunoregulatory and anti-inflammatory effects in this disease, and it could complement the effect of other Disease Modifying Treatments (DMT), such as Interferon-beta (IFN-beta). Here, our main goal was to evaluate the potential PCB benefits and its mechanisms of action to counteract the chronic EAE in mice. MOG(35-55)-induced EAE was implemented in C57BL/6 female mice. Clinical signs, pro-inflammatory cytokines levels by ELISA, qPCR in the brain and immunohistochemistry using precursor/mature oligodendrocytes cells antibodies in the spinal cord, were assessed. PCB enhanced the neurological condition, and waned the brain concentrations of IL-17A and IL-6, pro-inflammatory cytokines, in a dose-dependent manner. A down- or up-regulating activity of PCB at 1 mg/kg was identified in the brain on three (LINGO1, NOTCH1, and TNF-alpha), and five genes (MAL, CXCL12, MOG, OLIG1, and NKX2-2), respectively. Interestingly, a reduction of demyelination, active microglia/macrophages density, and axonal damage was detected along with an increase in oligodendrocyte precursor cells and mature oligodendrocytes, when assessed the spinal cords of EAE mice that took up PCB. The studies in vitro in rodent encephalitogenic T cells and in vivo in the EAE mouse model with the PCB/IFN-beta combination, showed an enhanced positive effect of this combined therapy. Overall, these results demonstrate the anti-inflammatory activity and the protective properties of PCB on the myelin and support its use with IFN-beta as an improved DMT combination for MS.

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