Brazilian green propolis modulates inflammation,
angiogenesis and fibrogenesis in intraperitoneal implant in mice
BMC Complement Altern Med, 2014 May 29;14(1):177
BACKGROUND:
Chronic inflammatory processes in the peritoneal cavity
develop as a result of ischemia, foreign body reaction, and trauma. Brazilian
green propolis, a beeswax product, has been shown to exhibit multiple actions
on inflammation and tissue repair. Our aim was to investigate the effects of
this natural product on the inflammatory, angiogenic, and fibrogenic components
of the peritoneal fibroproliferative tissue induced by a synthetic matrix.
METHODS:
Chronic inflammation was induced by placing polyether-polyurethane
sponge discs in the abdominal cavity of anesthetized Swiss mice. Oral
administration of propolis (500/mg/kg/day) by gavage started 24 hours after
injury for four days. The effect of propolis on peritoneal permeability was
evaluated through fluorescein diffusion rate 4 days post implantation. The
effects of propolis on the inflammatory (myeloperoxidase and
n-acetyl-beta-D-glucosaminidase activities and TNF-alpha levels), angiogenic
(hemoglobin content-Hb), and fibrogenic (TGF-beta1 and collagen deposition)
components of the fibrovascular tissue in the implants were determined 5 days
after the injury.
RESULTS:
Propolis was able to decrease intraperitoneal permeability.
The time taken for fluorescence to peak in the systemic circulation was 20 +/-
1 min in the treated group in contrast with 15 +/- 1 min in the control group.
In addition, the treatment was shown to down-regulate angiogenesis (Hb content)
and fibrosis by decreasing TGF-beta1 levels and collagen deposition in
fibroproliferative tissue induced by the synthetic implants. Conversely, the
treatment up-regulated inflammatory enzyme activities, TNF-alpha levels and
gene expression of NOS2 and IFN-gamma (23 and 7 fold, respectively), and of
FIZZ1 and YM1 (8 and 2 fold) when compared with the untreated group.
CONCLUSIONS:
These observations show for the first time the effects of
propolis modulating intraperitoneal inflammatory angiogenesis in mice and
disclose important action mechanisms of the compound (downregulation of
angiogenic components and activation of murine macrophage pathways).
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