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8-Methoxypsoralen Plus Ultraviolet A Reduces the Psoriatic Response to Imiquimod in a Murine Model.

Abstract
The effects of 8-Methoxypsoralen plus ultraviolet A (PUVA) or ultraviolet B (UVB) alone on imiquimod-induced psoriasis were examined in a mouse model. Mouse skin was treated with repetitive sub-phototoxic doses of PUVA or UVB before or during the induction of toll-like receptor 7/8 activation and psoriasis through the application of imiquimod. PUVA, to a greater degree than UVB, suppressed the established imiquimod-induced psoriatic phenotype, but pretreatment with PUVA prior to administration of imiquimod also reduced the susceptibility of murine skin to respond to imiquimod to a greater degree than did pretreatment with UVB. PUVA downregulated baseline levels of miRNA27a and 29a, as well as interferon-γ, interleukin-17 and -9, cytokines, which drive psoriatic inflammation. Microarray analysis showed enrichment of senescence pathway genes linked to upregulation of p16/p21 proteins after PUVA pretreatment. However, the anti-psoriatic effect of PUVA was lost when there was an interval of 7 days between final exposure to PUVA and the start of administration of imiquimod. This indicated that (UVB and) PUVA diminished imiquimod-induced established psoriatic inflammation, but also primed the skin in favour of a reduced responsiveness to toll-like receptor activation.
AuthorsNitesh Shirsath, Karin Wagner, Simone Tangermann, Michaela Schlederer, Christian Ringel, Lukas Kenner, Bernhard Brüne, Peter Wolf
JournalActa dermato-venereologica (Acta Derm Venereol) Vol. 98 Issue 6 Pg. 576-584 (Jun 08 2018) ISSN: 1651-2057 [Electronic] Sweden
PMID29582898 (Publication Type: Journal Article)
Chemical References
  • Aminoquinolines
  • Cytokines
  • Photosensitizing Agents
  • Imiquimod
  • Methoxsalen
Topics
  • Aminoquinolines
  • Animals
  • Cytokines (genetics, metabolism)
  • Disease Models, Animal
  • Female
  • Gene Expression Regulation (drug effects)
  • Imiquimod
  • Methoxsalen (pharmacology)
  • Mice, Inbred BALB C
  • PUVA Therapy
  • Photosensitizing Agents (pharmacology)
  • Psoriasis (chemically induced, genetics, metabolism, prevention & control)
  • Signal Transduction (drug effects)
  • Skin (drug effects, metabolism, pathology)
  • Time Factors

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