Imbalanced serum levels of resolvin E1 (RvE1) and leukotriene B4 (LTB4) in patients with allergic rhinitis.


Journal

Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 08 08 2020
accepted: 17 09 2020
revised: 10 09 2020
pubmed: 23 9 2020
medline: 19 5 2021
entrez: 22 9 2020
Statut: ppublish

Résumé

Timely and successful resolution of acute inflammation plays a crucial role in preventing the development of chronic airway inflammation in allergic rhinitis (AR). This study intends to assess the serum levels of pro-inflammatory leukotriene B4 (LTB4), anti-inflammatory mediators, including resolvin E1 (RvE1), RvD1, IL-10, and TGF-β, besides mRNA expression level of G-protein coupled receptor 120 (GPR120) and peroxisome proliferator-activated receptor-γ (PPAR-γ) receptors in peripheral blood leukocytes of AR patients. Thirty-seven AR patients and thirty age- and gender-matched healthy subjects were enrolled in this study. The serum levels of LTB4, RvE1, RvD1, IL-10, and TGF-β were measured using enzyme-linked immunosorbent assay (ELISA) technique, and the mRNA expression level of GPR120 and PPAR-γ was assessed by the real-time PCR method. The serum levels of RvE1 and LTB4 were significantly higher in patients with AR than in healthy subjects (P < 0.01 and P < 0.0001, respectively). However, a significantly lower ratio of RvE1 and RvD1 to LTB4 was found in patients with AR relative to healthy subjects (P < 0.05 and P < 0.0001, respectively). Likewise, the serum levels of both IL-10 and TGF-β cytokines were significantly reduced in patients with AR compared to healthy subjects (P < 0.01 and P < 0.0001, respectively). Furthermore, the mRNA expression of PPAR-γ was significantly lower in patients with AR than in healthy subjects (P < 0.05). Our findings indicate that imbalanced pro-resolving lipid mediator RvE1 and pro-inflammatory LTB4 might contribute to the defective airway inflammation-resolution and subsequent progression toward chronic inflammation in AR patients.

Identifiants

pubmed: 32960415
doi: 10.1007/s11033-020-05849-x
pii: 10.1007/s11033-020-05849-x
doi:

Substances chimiques

FFAR4 protein, human 0
IL10 protein, human 0
PPAR gamma 0
PPARG protein, human 0
Receptors, G-Protein-Coupled 0
Transforming Growth Factor beta 0
Interleukin-10 130068-27-8
Leukotriene B4 1HGW4DR56D
Eicosapentaenoic Acid AAN7QOV9EA
5S,12R,18R-trihydroxy-6Z,8E,10E,14Z,16E-eicosapentaenoic acid GND3JH08JA

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7745-7754

Subventions

Organisme : Deputy for Research and Technology, Kermanshah University of Medical Sciences
ID : 96043

Auteurs

Ramin Lotfi (R)

Lung Diseases and Allergy Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Student Research Committee, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Akram Davoodi (A)

Student Research Committee, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Seyed Hamidreza Mortazavi (SH)

Department of Pediatrics, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Ali Gorgin Karaji (A)

Department of Immunology, School of Medicine, Kermanshah University of Medical Sciences, PO-Box: 6714869914, Kermanshah, Iran.

Hanieh Tarokhian (H)

Department of Immunology, School of Medicine, Kermanshah University of Medical Sciences, PO-Box: 6714869914, Kermanshah, Iran.

Alireza Rezaiemanesh (A)

Department of Immunology, School of Medicine, Kermanshah University of Medical Sciences, PO-Box: 6714869914, Kermanshah, Iran.

Farhad Salari (F)

Department of Immunology, School of Medicine, Kermanshah University of Medical Sciences, PO-Box: 6714869914, Kermanshah, Iran. f.salari@kums.ac.ir.

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Classifications MeSH