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East Indian Sandalwood Oil Is a Phosphodiesterase Inhibitor: A New Therapeutic Option in the Treatment of Inflammatory Skin Disease.
Sharma, Manju; Levenson, Corey; Browning, John C; Becker, Emily M; Clements, Ian; Castella, Paul; Cox, Michael E.
Afiliação
  • Sharma M; The Vancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, BC, Canada.
  • Levenson C; Santalis Pharmaceuticals, Inc., San Antonio, TX, United States.
  • Browning JC; Texas Dermatology and Laser Specialists, San Antonio, TX, United States.
  • Becker EM; Texas Dermatology and Laser Specialists, San Antonio, TX, United States.
  • Clements I; Santalis Pharmaceuticals, Inc., San Antonio, TX, United States.
  • Castella P; Santalis Pharmaceuticals, Inc., San Antonio, TX, United States.
  • Cox ME; The Vancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, BC, Canada.
Front Pharmacol ; 9: 200, 2018.
Article em En | MEDLINE | ID: mdl-29593534
ABSTRACT
Cyclic adenosine monophosphate phosphodiesterases (PDEs) regulate pro-inflammatory cytokine production. One isoform, PDE4, is overactive in chronic relapsing inflammatory skin diseases psoriasis and eczema/atopic dermatitis, and in several cancers. East Indian sandalwood oil (EISO) has significant anti-inflammatory properties. Here, we report that 75% of pediatric eczema/atopic dermatitis patients treated with topical EISO formulations achieved a >50% reduction in their Eczema Area and Severity Index score. EISO treatment of a psoriasis model reduced PDE4 expression and reversed histopathology. EISO directly inhibited PDE enzymatic activity in vitro. In lipopolysaccharide-stimulated human dermal fibroblast, BEAS-2B, A549, and THP-1 cells, EISO suppressed total cellular PDE activity, PDE4, and 7 transcript levels, nuclear factor kappa B (NF-κB) activation, and pro-inflammatory cytokines/chemokine production. These results suggest that EISO anti-inflammatory activity is mediated through suppressing PDE activity, thus facilitating cAMP-regulated inhibition of NF-κB and indicate EISO as an attractive natural therapeutic for chronic and acute inflammatory disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Pharmacol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Pharmacol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá