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Perilla Fruit Water Extract Attenuates Inflammatory Responses and Alleviates Neutrophil Recruitment via MAPK/JNK-AP-1/c-Fos Signaling Pathway in ARDS Animal Model.
Ting, Nai-Chun; Chen, Yu-Hao; Chen, Jeng-Chang; Huang, Wen-Chung; Liou, Chian-Jiun; Chen, Li-Chen; Yang, Sien-Hung; Kuo, Ming-Ling.
Affiliation
  • Ting NC; Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Chen YH; Department of Microbiology and Immunology, Graduate Institute of Biomedical Sciences, Chang Gung University, Taoyuan, Taiwan.
  • Chen JC; Department of Surgery, Chang Gung Memorial Hospital-Linko, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Huang WC; Department of Medicine, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Liou CJ; Graduate Institute of Health Industry Technology Research Center for Food and Cosmetic Safety, Chang Gung University of Science and Technology, Taoyuan, Taiwan.
  • Chen LC; Research Center for Chinese Herbal Medicine College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan, Taiwan.
  • Yang SH; Division of Allergy, Asthma, and Rheumatology Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Kuo ML; Department of Pediatrics, New Taipei Municipal Tucheng Hospital, New Taipei, Taiwan.
Article in En | MEDLINE | ID: mdl-35815275
ABSTRACT
Airway respiratory distress syndrome (ARDS) is usually caused by a severe pulmonary infection. However, there is currently no effective treatment for ARDS. Traditional Chinese medicine (TCM) has been shown to effectively treat inflammatory lung diseases, but a clear mechanism of action of TCM is not available. Perilla fruit water extract (PFWE) has been used to treat cough, excessive mucus production, and some pulmonary diseases. Thus, we propose that PFWE may be able to reduce lung inflammation and neutrophil infiltration in a lipopolysaccharide (LPS)-stimulated murine model. C57BL/6 mice were stimulated with LPS (10 µg/mouse) by intratracheal (IT) injection and treated with three doses of PFWE (2, 5, and 8 g/kg) by intraperitoneal (IP) injections. To investigate possible mechanisms, A549 cells were treated with PFWE and stimulated with LPS. Our results showed that PFWE decreased airway resistance, neutrophil infiltration, vessel permeability, and interleukin (IL)-6 and chemokine (C-C motif) ligand 2 (CCL2/MCP-1) expressions in vivo. In addition, the PFWE inhibited the expression of IL-6, CCL2/MCP-1, chemokine (CXC motif) ligand 1 (CXCL1/GROα), and IL-8 in vitro. Moreover, PFWE also inhibited the MAPK/JNK-AP-1/c-Fos signaling pathway in A549 cells. In conclusion, we demonstrated that PFWE attenuated pro-inflammatory cytokine and chemokine levels and downregulated neutrophil recruitment through the MAPK/JNK-AP-1/c-Fos pathway. Thus, PFWE can be a potential drug to assist the treatment of ARDS.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Evid Based Complement Alternat Med Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Evid Based Complement Alternat Med Year: 2022 Document type: Article Affiliation country: