4.5 Article

Perilla Leaf Extract Attenuates Asthma Airway Inflammation by Blocking the Syk Pathway

期刊

MEDIATORS OF INFLAMMATION
卷 2021, 期 -, 页码 -

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HINDAWI LTD
DOI: 10.1155/2021/6611219

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资金

  1. National Natural Science Foundation of China [81973539, 81473398, 81803810]
  2. Beijing Natural Science Foundation Program [7182116]
  3. CAMS Initiative for Innovative Medicine [2016-I2M-2-006]
  4. Drug Innovation Major Project of China [2018ZX09711001-003-001]
  5. PUMC Graduate Innovation Fund [2019-1007-14]

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Perilla leaf extract (PLE) exhibits anti-allergic asthma effects by attenuating airway inflammation and might partly mediate through inhibiting the Syk pathway.
Perilla frutescens (L.) Britton is a classic herbal plant used widely against asthma in China. But its mechanism of beneficial effect remains undermined. In the study, the antiallergic asthma effects of Perilla leaf extract (PLE) were investigated, and the underlying mechanism was also explored. Results showed that PLE treatment significantly attenuated airway inflammation in OVA-induced asthma mice, by ameliorating lung pathological changes, inhibiting recruitment of inflammatory cells in lung tissues and bronchoalveolar lavage fluid (BALF), decreasing the production of inflammatory cytokines in the BALF, and reducing the level of immunoglobulin in serum. PLE treatment suppressed inflammatory response in antigen-induced rat basophilic leukemia 2H3 (RBL-2H3) cells as well as in OVA-induced human peripheral blood mononuclear cells (PBMCs). Furthermore, PLE markedly inhibited the expression and phosphorylation of Syk, NF-kappa B, PKC, and cPLA(2) both in vivo and in vitro. By cotreating with inhibitors (BAY61-3606, Rottlerin, BAY11-7082, and arachidonyl trifluoromethyl ketone) in vitro, results revealed that PLE's antiallergic inflammatory effects were associated with the inhibition of Syk and its downstream signals NF-kappa B, PKC, and cPLA(2). Collectively, the present results suggested that PLE could attenuate allergic inflammation, and its mechanism might be partly mediated through inhibiting the Syk pathway.

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