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Xiangpi shengji onitment promotes infected wound healing in rats via the PI3K/AKT/HIF-1α signaling pathway
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Xiangpi Shengji Onitment (XPSJO) is a hospital preparation commonly used
in clinic to treat large areas of bedsores and chronic non-healing
wounds. However, a complete understanding of the molecular mechanisms is
still lacking. This study used rats to explore the healing mechanisms of
XPSJO in promoting infected wound healing. Forty-five male Sprague
Dawley (SD) rats were randomly divided into model control group, XPSJO
group and basic fibroblast growth factor (bFGF) group. The wound
contraction was quantified on days 3, 7 and 14 after medication.
Hematoxylin and eosin stains were performed for histopathological
evaluation. The levels of tumour necrosis factor-α (TNF-α), interleukin
(IL)-1β, matrix metalloproteinase 2 (MMP2), MMP9 and vascular
endothelial growth factor (VEGF) were detected by enzyme-linked
immunosorbent assay (ELISA). Protein expression of PI3K, p-PI3K, AKT,
p-AKT and HIF-1α were detected by western blot analysis. XPSJO
significantly enhanced the wound healing rate, and more blood vessels
and fibroblasts were observed in the regenerated tissues in XPSJO
treatment group. ELISA results showed that XPSJO significantly decreased
the levels of TNF-α and IL-1β and increased the levels of VEGF in wound
tissue. XPSJO increased the levels of MMP2 and MMP9 in early stage of
wound healing. In addition, activated PI3K/AKT/HIF-1α signaling pathway
was detected in the XPSJO treatment group.
Title: Xiangpi shengji onitment promotes infected wound healing in rats via the PI3K/AKT/HIF-1α signaling pathway
Description:
Xiangpi Shengji Onitment (XPSJO) is a hospital preparation commonly used
in clinic to treat large areas of bedsores and chronic non-healing
wounds.
However, a complete understanding of the molecular mechanisms is
still lacking.
This study used rats to explore the healing mechanisms of
XPSJO in promoting infected wound healing.
Forty-five male Sprague
Dawley (SD) rats were randomly divided into model control group, XPSJO
group and basic fibroblast growth factor (bFGF) group.
The wound
contraction was quantified on days 3, 7 and 14 after medication.
Hematoxylin and eosin stains were performed for histopathological
evaluation.
The levels of tumour necrosis factor-α (TNF-α), interleukin
(IL)-1β, matrix metalloproteinase 2 (MMP2), MMP9 and vascular
endothelial growth factor (VEGF) were detected by enzyme-linked
immunosorbent assay (ELISA).
Protein expression of PI3K, p-PI3K, AKT,
p-AKT and HIF-1α were detected by western blot analysis.
XPSJO
significantly enhanced the wound healing rate, and more blood vessels
and fibroblasts were observed in the regenerated tissues in XPSJO
treatment group.
ELISA results showed that XPSJO significantly decreased
the levels of TNF-α and IL-1β and increased the levels of VEGF in wound
tissue.
XPSJO increased the levels of MMP2 and MMP9 in early stage of
wound healing.
In addition, activated PI3K/AKT/HIF-1α signaling pathway
was detected in the XPSJO treatment group.
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