Literature DB >> 20186670

Perioperative steroid administration inhibits angiogenic host tissue response to porous polyethylene (Medpor) implants.

S Ehrmantraut1, M W Laschke, D Merkel, C Scheuer, V Willnecker, A Meyer-Lindenberg, M D Menger, A Naumann.   

Abstract

Porous polyethylene (Medpor) is an alloplastic biomaterial, which is commonly used in plastic and reconstructive surgery. In the present study, we analyzed the effect of perioperative steroid administration on the inflammatory and angiogenic host tissue response to implanted Medpor. For this purpose, Medpor was implanted into the dorsal skinfold chamber of prednisolone-treated and vehicle-treated (control) balb/c mice and analyzed by means of intravital fluorescence microscopy over a 14-day period. Incorporation of the implants was evaluated by histology. An aortic ring assay and Western blot analyses were performed to determine in vitro the effect of prednisolone on angiogenesis. Implantation of Medpor did not induce a leukocytic inflammatory host tissue response. However, in prednisolone-treated and control animals giant cells could be detected at the interface between the implants and the surrounding granulation tissue as a typical indicator for a chronic foreign body reaction. Interestingly, perioperative prednisolone administration inhibited vascularisation of the implants, as indicated by a significantly decreased functional density of newly developing capillary blood vessels. Accordingly, prednisolone suppressed in vitro endothelial sprouting and tube formation in the aortic ring assay and reduced proliferating cell nuclear antigen (PCNA), Tie2, vascular endothelial growth factor (VEGF) and matrix metalloproteinase (MMP)-9 expression of murine endothelioma cells. In conclusion, prednisolone treatment inhibits the early vascularisation of Medpor implants due to direct inhibition of distinct angiogenic mechanisms. Therefore, perioperative steroid therapy should be avoided in case of Medpor implantation to achieve a rapid incorporation of the biomaterial at the implantation site.

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Year:  2010        PMID: 20186670     DOI: 10.22203/ecm.v019a11

Source DB:  PubMed          Journal:  Eur Cell Mater        ISSN: 1473-2262            Impact factor:   3.942


  9 in total

1.  [No cortisone following porous polyethylene implants].

Authors:  J M Hempel
Journal:  HNO       Date:  2011-03       Impact factor: 1.284

2.  [Tissue engineering using porous polyethylene implants].

Authors:  S Strieth
Journal:  HNO       Date:  2013-03       Impact factor: 1.284

3.  [Ear reconstruction using porous polyethylene implants. Effect of cortisone on edema reduction and healing process].

Authors:  A Naumann; S Ehrmantraut; V Willnecker; M D Menger; B Schick; M W Laschke
Journal:  HNO       Date:  2011-03       Impact factor: 1.284

4.  In vitro and in vivo evaluation of the anti-angiogenic actions of 4-hydroxybenzyl alcohol.

Authors:  M W Laschke; A E Vorsterman van Oijen; C Scheuer; M D Menger
Journal:  Br J Pharmacol       Date:  2011-06       Impact factor: 8.739

5.  [Porous polyethylene implants for ear reconstruction of middle to high-grade ear defects].

Authors:  A Naumann
Journal:  HNO       Date:  2011-02       Impact factor: 1.284

6.  Geraniol Suppresses Angiogenesis by Downregulating Vascular Endothelial Growth Factor (VEGF)/VEGFR-2 Signaling.

Authors:  Christine Wittig; Claudia Scheuer; Julia Parakenings; Michael D Menger; Matthias W Laschke
Journal:  PLoS One       Date:  2015-07-08       Impact factor: 3.240

7.  Inhibition of Hyaluronic Acid Synthesis Suppresses Angiogenesis in Developing Endometriotic Lesions.

Authors:  Carla N Olivares; Laura D Alaniz; Michael D Menger; Rosa I Barañao; Matthias W Laschke; Gabriela F Meresman
Journal:  PLoS One       Date:  2016-03-28       Impact factor: 3.240

8.  Delayed onset porous polyethylene implant-related inflammation after orbital blowout fracture repair: four case reports.

Authors:  Orapan Aryasit; Danny S Ng; Alice S C Goh; Kyung In Woo; Yoon-Duck Kim
Journal:  BMC Ophthalmol       Date:  2016-07-07       Impact factor: 2.209

9.  Prevascularization of collagen-glycosaminoglycan scaffolds: stromal vascular fraction versus adipose tissue-derived microvascular fragments.

Authors:  Thomas Später; Florian S Frueh; Ruth M Nickels; Michael D Menger; Matthias W Laschke
Journal:  J Biol Eng       Date:  2018-11-13       Impact factor: 4.355

  9 in total

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