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Combined therapy of adipose-derived stem cells and photobiomodulation on accelerated bone healing of a critical size defect in an osteoporotic rat model.
Asgari, Mehrdad; Gazor, Rouhallah; Abdollahifar, Mohammad-Amin; Fadaei Fathabady, Fatemeh; Zare, Fatemeh; Norouzian, Mohsen; Amini, Abdollah; Khosravipour, Armin; Kiani, Pejman; Atashgah, Rahimeh B; Rezaei, Fatemehsadat; Ghoreishi, Seyed Kamran; Chien, Sufan; Hamblin, Michael R; Bayat, Mohammad.
Affiliation
  • Asgari M; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: mehrdad_vhf@yahoo.com.
  • Gazor R; Department of Anatomy, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran. Electronic address: rouhollahgazor@gmail.com.
  • Abdollahifar MA; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: m_amin58@yahoo.com.
  • Fadaei Fathabady F; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: Fatemehfadaeifathabadi@gmail.com.
  • Zare F; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: fatemezare81@gmail.com.
  • Norouzian M; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: norozian93@gmail.com.
  • Amini A; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: dr.amini@sbmu.ac.ir.
  • Khosravipour A; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: a.khosravipor@gmail.com.
  • Kiani P; Department of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Science, Tehran, Iran. Electronic address: pkia59@yahoo.com.
  • Atashgah RB; Department of Pharmaceutical Biomaterials, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, 13169-43551, Iran. Electronic address: atashgah.r@gmail.com.
  • Rezaei F; University of Kentucky College of Pharmacy, 789 South Limestone, Lexington, KY, 40536, USA. Electronic address: journalist.best@gmail.com.
  • Ghoreishi SK; Department of Statistics, Qom University, Qom, Iran. Electronic address: atty_ghoreishi@yahoo.com.
  • Chien S; Price Institute of Surgical Research, University of Louisville, Noveratech LLC, Louisville, KY, USA. Electronic address: sufan.chien@louisville.edu.
  • Hamblin MR; Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, USA; Laser Research Centre, Faculty of Health Science, University of Johannesburg, Doornfontein, 2028, South Africa. Electronic address: Hamblin@helix.mgh.harvard.edu.
  • Bayat M; Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Price Institute of Surgical Research, University of Louisville, Noveratech LLC, Louisville, KY, USA. Electronic address: mohbayat@sbmu.ac.ir.
Biochem Biophys Res Commun ; 530(1): 173-180, 2020 09 10.
Article in En | MEDLINE | ID: mdl-32828282
ABSTRACT
We investigated the impact of human demineralized bone matrix (hDBM) plus adipose-derived stem cells (hADS) plus photobiomodulation (PBM) on a critical-sized femoral defect (CSFD) in ovariectomy induced osteoporosis in rats. There were 6 groups as follows. In group 1 (control, C), only CSFDs were created. Groups 2-6 were implanted with DBM into the CSFD (DBM-CSFD). In group 2 (S), only DBM was transplanted into the CSFD. In group 3 (S + PBM), the DBM-CSFDs were treated with PBM. In group 4, the DBM-CSFDs were treated with alendronate (S + ALN). In group 5, ADSs were seeded into DBM-CSFD (S + ADS). In group 6, ADSs were seeded into DBM-CSFD and the CSFDs were treated with PBM (S + PBM + ADS). At week eight (catabolic phase of bone repair), the S + ALN, S + PBM + ADS, S + PBM, and S + ADS groups all had significantly increased bone strength than the S group (ANOVA, p = 0.000). The S + PBM, S + PBM + ADS, and S + ADS groups had significantly increased Hounsfield unit than the S group (ANOVA, p = 0.000). ALN, ADS, and PBM significantly increased healed bone strength in an experimental model of DBM-treated CSFD in the catabolic phase of bone healing in osteoporotic rats. However, ALN alone and PBM plus ADS were superior to the other protocols.
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Full text: 1 Database: MEDLINE Therapeutic Methods and Therapies TCIM: Terapias_energeticas Main subject: Osteoporosis / Bone Matrix / Low-Level Light Therapy / Mesenchymal Stem Cell Transplantation / Mesenchymal Stem Cells Language: En Journal: Biochem Biophys Res Commun Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Therapeutic Methods and Therapies TCIM: Terapias_energeticas Main subject: Osteoporosis / Bone Matrix / Low-Level Light Therapy / Mesenchymal Stem Cell Transplantation / Mesenchymal Stem Cells Language: En Journal: Biochem Biophys Res Commun Year: 2020 Type: Article