Effects of bromopride on expression of metalloproteinases and interleukins in left colonic anastomoses: an

S M Silva1, M S Jerônimo2, I Silva-Pereira3

  • 1Programa de Pós-Graduação em Ciências Médicas, Faculdade de Medicina, Universidade de Brasília, Brasília, DF, Brasil.

Insights

Bromopride alters matrix metalloproteinase (MMP) and interleukin (IL) gene expression in rat colonic anastomoses, impacting healing. These changes vary with sepsis presence and time post-surgery, requiring further investigation.

Area of Science:

  • Gastroenterology
  • Surgical Research
  • Molecular Biology

Background:

  • Anastomotic dehiscence is a critical complication in colorectal surgery.
  • Matrix metalloproteinases (MMPs) and interleukins (ILs) are key markers of anastomotic healing.
  • Understanding factors influencing healing is crucial for improving surgical outcomes.

Purpose of the Study:

  • To investigate the effect of bromopride on MMP and cytokine gene expression in rat colonic anastomoses.
  • To assess these effects in the presence and absence of induced abdominal sepsis.
  • To analyze changes at different time points (3rd and 7th postoperative days).

Main Methods:

  • 80 rats underwent left colonic anastomosis and were divided into sepsis/no sepsis and bromopride/saline subgroups.
  • Gene expression analysis of MMPs (MMP-1α, MMP-8, MMP-13) and cytokines (IL-1β, IL-6, IL-10, TNF-α, IFN-γ) was performed.
  • Samples were collected on the 3rd and 7th postoperative days.

Main Results:

  • Bromopride increased MMP-1α, MMP-13, IL-6, IFN-γ, and IL-10 expression on POD 3.
  • By POD 7, MMP transcripts were negatively modulated, while IL transcripts were positively modulated by bromopride.
  • In sepsis, bromopride altered MMP and cytokine expression differently on POD 3 and POD 7.

Conclusions:

  • Bromopride significantly interferes with MMP and IL gene expression during anastomotic healing in rats.
  • The observed effects are modulated by the presence of sepsis and the time elapsed post-surgery.
  • Further research is necessary to correlate these molecular changes with the actual healing process and clinical outcomes.