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Square wave voltammetry on screen printed electrodes: comparison to ferric reducing antioxidant power in plasma from model laboratory animal (Grey Partridge) and comparison to standard antioxidants
Miroslav Pohanka, Hana Bandouchova, Kristina Vlckova, Jana Zdarova Karasova, Kamil Kuca, Veronika Damkova, Lucie Peckova, Frantisek Vitula, Jiri Pikula
Language English Country Czech Republic
NLK
Free Medical Journals
from 2003 to 2013
Freely Accessible Science Journals
from 2003 to 2013
ROAD: Directory of Open Access Scholarly Resources
from 2002
- MeSH
- Antioxidants chemistry metabolism MeSH
- Biochemistry methods MeSH
- Biosensing Techniques instrumentation utilization MeSH
- Electrochemistry methods MeSH
- Financing, Organized MeSH
- Glutathione chemistry blood MeSH
- Blood MeSH
- Ascorbic Acid chemistry blood MeSH
- Uric Acid chemistry blood MeSH
- Models, Animal MeSH
- Oxidative Stress physiology immunology drug effects MeSH
- Birds blood MeSH
- Reactive Oxygen Species chemistry metabolism MeSH
To resolve the problem of the insufficient availability of seed cells and to provide seed cells for tissue engineering research, an immortalized human bone marrow stromal stem cell line (MSCxj cells) was established in our department to investigate the ectopic osteogenesis of MSCxj cells. MSCxjs were grown with a heterogeneous bone scaffold for 48 h. Three groups were included: A: MSCxjs of 35 PDs were maintained with heterogeneous bone; B: MSCxjs of 128 PDs were maintained with heterogeneous bone; and C: heterogeneous bone alone. Tetracycline fluorescence staining, H&E staining, and ponceau staining, immunohistochemistry and bone histomorphometry were performed. At the same time, scanning electron microscopy was conducted to detect the growth of MSCxjs and heterogeneous bone. Scanning electron microscopy showed favorable adherence of MSCxjs to heterogeneous bone. A large number of newly generated filamentous extracellular matrix and fine granular materials were found to cover the cells. The results from staining showed that the osteogenesis was not obvious in group A/B 4 weeks after transplantation. Eight weeks after implantation, osteoid matrix deposition was noted in and around the heterogeneous bone in group A/B. Twelve weeks after implantation, osteogenesis was increased in group A/B. There were no significant differences in the time course for bone formation and the amount of newly generated bone between group A/B. Like primary hBMSCs, MSCxj cells have favourable ectopic osteogenesis and can be applied as seeded cells in bone tissue engineering.
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Lit.: 30
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- $a Square wave voltammetry on screen printed electrodes: comparison to ferric reducing antioxidant power in plasma from model laboratory animal (Grey Partridge) and comparison to standard antioxidants / $c Miroslav Pohanka, Hana Bandouchova, Kristina Vlckova, Jana Zdarova Karasova, Kamil Kuca, Veronika Damkova, Lucie Peckova, Frantisek Vitula, Jiri Pikula
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- $a Faculty of Military Health Sciences, University of Defence, Trebesska 1575, 500 01 Hradec Kralove
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- $a Lit.: 30
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- $a To resolve the problem of the insufficient availability of seed cells and to provide seed cells for tissue engineering research, an immortalized human bone marrow stromal stem cell line (MSCxj cells) was established in our department to investigate the ectopic osteogenesis of MSCxj cells. MSCxjs were grown with a heterogeneous bone scaffold for 48 h. Three groups were included: A: MSCxjs of 35 PDs were maintained with heterogeneous bone; B: MSCxjs of 128 PDs were maintained with heterogeneous bone; and C: heterogeneous bone alone. Tetracycline fluorescence staining, H&E staining, and ponceau staining, immunohistochemistry and bone histomorphometry were performed. At the same time, scanning electron microscopy was conducted to detect the growth of MSCxjs and heterogeneous bone. Scanning electron microscopy showed favorable adherence of MSCxjs to heterogeneous bone. A large number of newly generated filamentous extracellular matrix and fine granular materials were found to cover the cells. The results from staining showed that the osteogenesis was not obvious in group A/B 4 weeks after transplantation. Eight weeks after implantation, osteoid matrix deposition was noted in and around the heterogeneous bone in group A/B. Twelve weeks after implantation, osteogenesis was increased in group A/B. There were no significant differences in the time course for bone formation and the amount of newly generated bone between group A/B. Like primary hBMSCs, MSCxj cells have favourable ectopic osteogenesis and can be applied as seeded cells in bone tissue engineering.
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