4.7 Article

Therapeutic efficacy of Scutellaria baicalensis Georgi against psoriasis-like lesions via regulating the responses of keratinocyte and macrophage

Journal

BIOMEDICINE & PHARMACOTHERAPY
Volume 155, Issue -, Pages -

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.113798

Keywords

Psoriasis; Scutellaria baicalensis extract; Macrophage; Keratinocyte; Inflammation; Oxidation; Network analysis

Funding

  1. Ministry of Science and Technology [MOST109-2320-B-039-040, MOST108-2320-B-182-024-MY3]
  2. Chang Gung Memorial Hospital [CMRPD1K0341, BMRP445]

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Scutellaria baicalensis extract has a pharmaceutical efficacy in modulating the microenvironment created by macrophages and keratinocytes in psoriasis. The extract can reduce psoriatic lesions and inhibit the activation and infiltration of macrophages. It also protects against oxidative damage to DNA and proteins.
Psoriasis is a chronic and recurrent skin problem that affects 3% of the global population. Nowadays, most medicines may not promise a complete cure for patients with psoriasis because of the development of phar-macoresistance and the side effects of drugs due to the microenvironment impact in the context of skin imbal-ance. Herein, we attempt to explore the pharmaceutical efficacy of Scutellaria baicalensis (S. baicalensis) in modulating the microenvironment created by macrophages and keratinocytes in psoriasis. The results indicated that treatment of S. baicalensis extract significantly reduced the thickness of epidermis and attenuated psoriatic lesions. Moreover, S. baicalensis extract obviously inhibited the activation and infiltration of macrophages by alleviating inflammatory factors such as nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B) and cyclooxygenase-2 (COX-2). The administration of S. baicalensis extract also remarkably abolished oxidative damage upon DNA and proteins, which attributed to the activation of nuclear factor erythroid 2-related factor-2 (Nrf2) and heme oxygenase-1 (HO-1). The network analysis of redox proteomics and cytokine profiles suggested that S. baicalensis administration regulated the specific pathways associated with oxidative stress, inflammation and cytokine signaling cascades to ameliorate the macrophage-targeted responses and subsequently arrest pro-liferation of keratinocytes. Collectively, our findings highlighted the importance of S. baicalensis application in reprogramming microenvironment to provide an alternative and complementary intervention for long-term psoriatic therapy.

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