Combination of Merocel sponge with Lipopolysaccharide to establish rat rhinosinusitis model

Mengmeng Sun1, Junjie Yang2, Jiayu Liu2

  • 1Key Laboratory of Prescription Effect and Clinical Evaluation of State Administration of Traditional Chinese Medicine of China, School of Pharmacy, Binzhou Medical University, Yantai, Shandong, China; Key Laboratory of Molecular Pharmacology and Drug Evaluation, School of Pharmacy, Ministry of Education, Yantai University, Yantai, Shandong, China.

Abstract

Insights

This study successfully created a rat rhinosinusitis model using Lipopolysaccharide (LPS) and merocel sponge, revealing key inflammatory markers and mechanisms.

Area of Science:

  • Otorhinolaryngology
  • Immunology
  • Pathology

Background:

  • Rhinosinusitis is a common condition with complex pathophysiology.
  • Developing reliable animal models is crucial for understanding disease mechanisms and testing therapies.

Purpose of the Study:

  • To establish a feasible rat model of rhinosinusitis by combining merocel sponge-induced nasal obstruction with Lipopolysaccharide (LPS) instillation.
  • To investigate the underlying mechanisms of inflammation and tissue damage in this model.

Main Methods:

  • Established rhinosinusitis models in Sprague Dawley rats using merocel sponge packing, LPS instillation, or both.
  • Assessed nasal symptoms, performed histopathological and Transmission Electron Microscopy (TEM) analyses of sinus tissue.
  • Quantified serum levels of Tumor Necrosis Factor-alpha (TNF-α) and Interleukin-6 (IL-6).
  • Detected protein expression of Aquaporin-5 (AQP5), Occludin, Toll-Like Receptor-4 (TLR4), MyD88, and p-p65 via Western blot.

Main Results:

  • The combined merocel sponge and LPS group exhibited significantly higher sinusitis scores compared to control and LPS-only groups.
  • Histopathology revealed degeneration of respiratory epithelia, cilia detachment, and inflammatory cell infiltration in the maxillary sinus.
  • Elevated serum levels of TNF-α and IL-6 were observed.
  • Decreased expression of AQP5 and Occludin, alongside increased expression of TLR4, MyD88, and p-p65, indicated inflammatory pathway activation.

Conclusions:

  • Successfully established a novel rat rhinosinusitis model using merocel sponge and LPS.
  • The model effectively mimics key pathological features of rhinosinusitis and demonstrates the involvement of the TLR4/MyD88/NF-κB pathway in LPS-induced inflammation.

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