Critical-size bone defect repair using amniotic fluid stem cell/collagen constructs: effect of oral ferutinin treatment in rats

Life Sci. 2015 Jan 15:121:174-83. doi: 10.1016/j.lfs.2014.10.020. Epub 2014 Nov 5.

Abstract

Aims: This study aims to evaluate the bone regeneration in a rat calvarias critical size bone defect treated with a construct consisting of collagen type I and human amniotic fluid stem cells (AFSCs) after oral administration of phytoestrogen ferutinin.

Main methods: In 12 week old male rats (n=10), we performed two symmetric full-thickness cranial defects on each parietal region, and a scaffold was implanted into each cranial defect. The rats were divided into four groups: 1) collagen scaffold, 2) collagen scaffold+ferutinin at a dose of 2mg/kg/5 mL, 3) collagen scaffold + AFSCs, and 4) collagen scaffold + AFSCs + ferutinin. The rats were sacrificed after 4 weeks, and the calvariae were removed, fixed, embedded in paraffin and cut into 7 μm thick sections. Histomorphometric measures, immunohistochemical and immunofluorescence analyses were performed on the paraffin sections.

Key findings: The histomorphometric analysis on H&E stained sections showed a significant increase in the regenerated area of the 4th group compared with the other groups. Immunohistochemistry performed with a human anti-mitochondrial antibody showed the presence of AFSCs 4 weeks after the transplant. Immunofluorescence analysis revealed the presence of osteocalcin and estrogen receptors (ERα and GPR30) in all groups, with a greater expression of all markers in samples where the scaffold was treated with AFSCs and the rats were orally administered ferutinin.

Significance: Our results demonstrated that the oral administration of ferutinin is able to improve the bone regeneration of critical-size bone defects in vivo that is obtained with collagen-AFSCs constructs.

Keywords: AFSCs; Bone regeneration; Collagen scaffold; Ferutinin; Rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amniotic Fluid / cytology*
  • Animals
  • Benzoates / pharmacology*
  • Bone Development / drug effects*
  • Bridged Bicyclo Compounds / pharmacology
  • Cell Differentiation / drug effects
  • Cell Survival / drug effects
  • Collagen / pharmacology*
  • Cycloheptanes / pharmacology*
  • Estrogen Receptor alpha / metabolism
  • Humans
  • Male
  • Osteocalcin / metabolism
  • Rats
  • Receptors, G-Protein-Coupled / metabolism
  • Sesquiterpenes / pharmacology*
  • Stem Cell Transplantation*

Substances

  • Benzoates
  • Bridged Bicyclo Compounds
  • Cycloheptanes
  • Estrogen Receptor alpha
  • Gper1 protein, rat
  • Receptors, G-Protein-Coupled
  • Sesquiterpenes
  • Osteocalcin
  • 4-oxy-6-(4-oxybezoyloxy)dauc-8,9-en
  • Collagen