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Anti-inflammatory Effect of Shea Butter Extracts in Canine Keratinocytes 원문보기

Journal of veterinary clinics = 한국임상수의학회지, v.38 no.1, 2021년, pp.27 - 31  

Lim, Dahye (Department of Veterinary Dermatology, College of Veterinary Medicine, Kyungpook National University) ,  Bae, Seulgi (Department of Veterinary Dermatology, College of Veterinary Medicine, Kyungpook National University) ,  Oh, Taeho (Department of Veterinary Dermatology, College of Veterinary Medicine, Kyungpook National University)

Abstract AI-Helper 아이콘AI-Helper

Shea butter (Vitellaria paradoxa) is a fat extracted from shea tree nuts and contains relatively high levels of non-glycerides. Triterpenes, the main non-glyceride component, exhibit a variety of biological activities such as antitumor, antibacterial, and anti-inflammatory. Shea butter extract (SBE)...

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제안 방법

  • To evaluate the relative anti-inflammatory effect of SBE, further study is needed. Furthermore, this study evaluated the anti-inflammatory effect of SBE against several cytokines and was performed in vitro. Further study to evaluate the safety and clinical effectiveness of SBE in canines is needed.
  • In human medicine, shea butter has been used as a topical agent in skincare and to treat various skins disorders. In this study, we evaluated the cytotoxicity and anti-inflammatory effects of SBE in canine epidermal progenitor keratinocytes (CPEK).

데이터처리

  • 0 (Systat Software; USA). Differences between groups were assessed with one-way ANOVA. P-values<0.

이론/모형

  • In this study, we evaluated the cytotoxicity and anti inflammatory effects of SBE in lipopolysaccharide (LPS)-induced inflammation in canine keratinocytes, using the CCK-8 assay and ELISA.
  • The cytotoxic effects of LPS and SBE in CPEK cells were assessed using the CCK-8 assay. Based on the results of the CCK-8 assays, the concentrations of LPS and SBE used to treat cells before ELISA assays were selected.
  • The cytotoxicity of LPS in CPEK cells was evaluated using the CCK-8 assay (Table 1). Table 1.
  • The levels of IL-1, IL-8, IL-12, and TNF- were measured to evaluate the anti-inflammatory effect of SBE in LPS-induced inflammation of CPEK cells using ELISA assays. The CPEK cells were divided into Control (no treatment), LPS-treated, and LPS+SBE-treated groups.
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참고문헌 (30)

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