In vivo
Evaluation of inflammatory mediators in an acute cystitis model.
Cyclophosphamide-induced cystitis is a well-characterized model of subacute, inflammatory visceral pain in rodents. This preclinical model is usually associated with urinary bladder inflammation, bladder overactivity and referred mechanical pain.
Rat.
This is a model of acute urinary bladder inflammation, characterized by high levels of pro-inflammatory cytokines, chemokine and adhesion molecules in the urinary bladder, and high levels of lipid derived mediators in urines.
Compounds that produce positive effects in this model include: non-steroidal anti-inflammatory drugs (aspirin and ibuprofen).
Urinary bladder inflammation is assessed at different time points after intraperitoneal injection of cyclophosphamide.
Inflammatory mediators are quantified in urinary bladders and urines using Multiplex technology, EIA or ELISA assays.
Compounds can be administered via various routes (i.v., i.p., s.c., p.o.).
Inflammatory parameters: tissue wet weight, bladder wall thickness, macroscopic damage (edema and hemorrhage), microscopic analysis.
Inflammatory mediators: arachidonic acid metabolites (PGE2, lipoxin A4, 15-epi lipoxin), pro-inflammatory cytokines (IL-1b, IL-6), chemokines, adhesion molecules (in collaboration with Ambiotis and UMR1043 Inserm).
UROsphere can also evaluate the feasibility of additional biomarkers to meet clients’ needs.
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