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Abstract Title:

Anti-inflammatory effects of Perilla frutescens in activated human neutrophils through two independent pathways: Src family kinases and Calcium.

Abstract Source:

Sci Rep. 2015 Dec 14 ;5:18204. Epub 2015 Dec 14. PMID: 26659126

Abstract Author(s):

Chun-Yu Chen, Yann-Lii Leu, Yu Fang, Chwan-Fwu Lin, Liang-Mou Kuo, Wei-Che Sung, Yung-Fong Tsai, Pei-Jen Chung, Ming-Chung Lee, Yu-Ting Kuo, Hsuan-Wu Yang, Tsong-Long Hwang

Article Affiliation:

Chun-Yu Chen

Abstract:

The leaves of Perilla frutescens (L.) Britt. have been traditionally used as an herbal medicine in East Asian countries to treat a variety diseases. In this present study, we investigated the inhibitory effects of P. frutescens extract (PFE) on N-formyl-Met-Leu-Phe (fMLF)-stimulated human neutrophils and the underlying mechanisms. PFE (1, 3, and 10 μg/ml) inhibited superoxide anion production, elastase release, reactive oxygen species formation, CD11b expression, and cell migration in fMLF-activated human neutrophils in dose-dependent manners. PFE inhibited fMLF-induced phosphorylation of the Src family kinases (SFKs), Src (Tyr416) and Lyn(Tyr396), and reduced their enzymatic activities. Both PFE and PP2 (a selective inhibitor of SFKs) reduced the phosphorylation of Burton's tyrosine kinases (Tyr223) and Vav (Tyr174) in fMLF-activated human neutrophils. Additionally, PFE decreased intracellular Ca(2+) levels ([Ca(2+)]i), whereas PP2prolonged the time required for [Ca(2+)]i to return to its basal level. Our findings indicated that PFE effectively regulated the inflammatory activities of fMLF-activated human neutrophils. The anti-inflammatory effects of PFE on activated human neutrophils were mediated through two independent signaling pathways involving SFKs (Src and Lyn) and mobilization of intracellular Ca(2+).

Study Type : In Vitro Study

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Sayer Ji
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