| Literature DB >> 33889673 |
Jose Manuel Cóndor Capcha1,2, Roberto S Moreira3, Camila E Rodrigues1, Marcelo A D Silveira1, Lucia Andrade1, Samirah A Gomes2.
Abstract
Sepsis is a dysregulated hyperinflammatory disease caused by infection. Sepsis leads to multiple organ dysfunction syndrome (MODS), which is associated with high rates of mortality. The cecal ligation and puncture (CLP) model has been widely used in animals and has become the gold-standard method of replicating features of sepsis in humans. Despite several studies and modified CLP protocols, there are still open questions regarding the multifactorial determinants of its reproducibility and medical significance. In our protocol, which is also aimed at mimicking the sepsis observed in clinical practice, male Wistar rats are submitted to CLP with adequate fluid resuscitation (0.15 M NaCl, 25 ml/kg BW i.p.) immediately after surgery. At 6 h after CLP, additional fluid therapy (0.15 M NaCl, 25 ml/kg BW s.c.) and antibiotic therapy with imipenem-cilastatin (single dose of 14 mg/kg BW s.c.) are administered. The timing of the fluid and antibiotic therapy correspond to the initial care given when patients are admitted to the intensive care unit. This model of sepsis provides a useful platform for simulating human sepsis and could lay the groundwork for the development of new treatments.Entities:
Keywords: Acute Kidney Injury; Animal Model; Cecal ligation and puncture (CLP); Organ dysfunction; Rats; Sepsis
Year: 2021 PMID: 33889673 PMCID: PMC8054174 DOI: 10.21769/BioProtoc.3979
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325