Experimental and Therapeutic Medicine · 2017 · 10 citations · 15 references
MedicinePharmacologyPharmacotherapyInflammationMolecular PharmacologySepsisAnti-inflammatory PharmacologyCholinergic PharmacologyInflammation PharmacologyInflammatory SignalingSepsis PathophysiologySepsis PharmacotherapyAnti-inflammatory Drug MechanismsAnti-inflammatory TherapeuticsCombined Drug Effect ModelsHistopathological LesionsNicotinic Acetylcholine Receptor AgonismPlant PolysaccharidesSepsis-associated Cytokine ResponseSepsis-associated Inflammation
polysaccharides (APS) in combination with ibuprofen (IBU) in the treatment of sepsis and the underlying mechanism. The combined drug treatment was evaluated in a rat model of cecal ligation and puncture (CLP). The serum concentrations of tumor necrosis factor (TNF)-α, interleukin (IL)-6 and acetylcholine (ACh) were determined. Nicotinic acetylcholine (nAChR) α7 receptor expression and histopathological changes in the lung tissue were also observed. When compared with untreated rats and rats treated with either component alone, the combined treatment significantly decreased the production of TNF-α and IL-6 (P<0.05), and increased nAChR α7 receptor mRNA expression and the release of ACh in the serum (P<0.05). These results demonstrated that APS combined with IBU can effectively reduce the generation of inflammatory mediators in the serum of CLP-induced septic rats. These effects may be mediated via a cholinergic anti-inflammatory pathway involving nAChR α7.
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Immunodesign of experimental sepsis by cecal ligation and puncture
Daniel Rittirsch, Markus Huber‐Lang, Michael A. Flierl et al. · Nature Protocols · 2008 · 2.2K citations · Full text