Echinochrome A Treatment Alleviates Atopic Dermatitis-like Skin Lesions in NC/Nga Mice via IL-4 and IL-13 Suppression.
Hyeong Rok YunSang Woo AhnBomin SeolElena A VasilevaNatalia P MishchenkoSergey A FedoreyevValentin A StonikJin HanKyung Soo KoByoung Doo RheeJung Eun SeolHyoung Kyu KimPublished in: Marine drugs (2021)
Atopic dermatitis (AD) is a chronic inflammatory skin disease in which skin barrier dysfunction leads to dryness, pruritus, and erythematous lesions. AD is triggered by immune imbalance and oxidative stress. Echinochrome A (Ech A), a natural pigment isolated from sea urchins, exerts antioxidant and beneficial effects in various inflammatory disease models. In the present study, we tested whether Ech A treatment alleviated AD-like skin lesions. We examined the anti-inflammatory effect of Ech A on 2,4-dinitrochlorobenzene (DNCB)-induced AD-like lesions in an NC/Nga mouse model. AD-like skin symptoms were induced by treatment with 1% DNCB for 1 week and 0.4% DNCB for 5 weeks in NC/Nga mice. The results showed that Ech A alleviated AD clinical symptoms, such as edema, erythema, and dryness. Treatment with Ech A induced the recovery of epidermis skin lesions as observed histologically. Tewameter® and Corneometer® measurements indicated that Ech A treatment reduced transepidermal water loss and improved stratum corneum hydration, respectively. Ech A treatment also inhibited inflammatory-response-induced mast cell infiltration in AD-like skin lesions and suppressed the expression of proinflammatory cytokines, such as interferon-γ, interleukin-4, and interleukin-13. Collectively, these results suggest that Ech A may be beneficial for treating AD owing to its anti-inflammatory effects.
Keyphrases
- atopic dermatitis
- oxidative stress
- mouse model
- inflammatory response
- soft tissue
- randomized controlled trial
- anti inflammatory
- clinical trial
- metabolic syndrome
- poor prognosis
- immune response
- high glucose
- signaling pathway
- long non coding rna
- ischemia reperfusion injury
- heat shock protein
- induced apoptosis
- binding protein