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An in vitro model to explore subchondral perfusion and intraosseous pressure

BACKGROUND: Little is known about subchondral perfusion physiology. We developed a 3Rs (Replace, Reduce, Refine) compliant in vitro calf foot model to explore perfusion and intraosseous pressure (IOP). METHODS: Calf feet were catheterised and perfused with serum. IOP was measured at three sites, the...

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Autores principales: Beverly, Michael, Murray, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717224/
https://www.ncbi.nlm.nih.gov/pubmed/31471704
http://dx.doi.org/10.1186/s40634-019-0207-3
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author Beverly, Michael
Murray, David
author_facet Beverly, Michael
Murray, David
author_sort Beverly, Michael
collection PubMed
description BACKGROUND: Little is known about subchondral perfusion physiology. We developed a 3Rs (Replace, Reduce, Refine) compliant in vitro calf foot model to explore perfusion and intraosseous pressure (IOP). METHODS: Calf feet were catheterised and perfused with serum. IOP was measured at three sites, the metacarpal diaphysis (MCD), metacarpal subchondral epiphysis (MCS) and proximal phalanx diaphysis (PPD) using intraosseous needles with pressure transducers and digital recorders. Fresh (< 4 h post mortem) and old feet (> 4 h post mortem) were perfused at different pressures, with and without a proximal tourniquet. RESULTS: There was a wide range in basal IOP with a mean IOP of 30.0 mmHg, SD 14.4, range 7.6 mmHg to 52.7 mmHg (n = 40 records) in 15 subjects. There was no significant difference between the three sites tested (p = 0.54, 0.12 and 0.051). At each individual site IOP correlated with perfusion pressure (r = 0.993). With a proximal venous tourniquet, IOP increased from 15.1 mmHg (SD 11.3 mmHg) to 44.9 mmHg (SD 24 mmHg), p < 0.0001, n = 9. Filling and emptying curves during perfusion and with using a tourniquet were similar, indicating that the model behaves in an elastic hydrodynamic manner. In fresh feet IOP peaked after about 1 min irrespective of perfusion pressure, possibly due to auto regulation. Older feet showed a continuously rising IOP and became oedematous. There was no significant difference in IOP between fresh and old feet perfused with serum at 150 cms pressure for 1 min. CONCLUSION: Though basal intraosseous pressure varies, IOP behaves predictably. IOP measurements reflect the perfusion microclimate at the individual needle tip. This 3Rs compliant model will be used for further exploration of subchondral perfusion physiology with loading.
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spelling pubmed-67172242019-09-13 An in vitro model to explore subchondral perfusion and intraosseous pressure Beverly, Michael Murray, David J Exp Orthop Research BACKGROUND: Little is known about subchondral perfusion physiology. We developed a 3Rs (Replace, Reduce, Refine) compliant in vitro calf foot model to explore perfusion and intraosseous pressure (IOP). METHODS: Calf feet were catheterised and perfused with serum. IOP was measured at three sites, the metacarpal diaphysis (MCD), metacarpal subchondral epiphysis (MCS) and proximal phalanx diaphysis (PPD) using intraosseous needles with pressure transducers and digital recorders. Fresh (< 4 h post mortem) and old feet (> 4 h post mortem) were perfused at different pressures, with and without a proximal tourniquet. RESULTS: There was a wide range in basal IOP with a mean IOP of 30.0 mmHg, SD 14.4, range 7.6 mmHg to 52.7 mmHg (n = 40 records) in 15 subjects. There was no significant difference between the three sites tested (p = 0.54, 0.12 and 0.051). At each individual site IOP correlated with perfusion pressure (r = 0.993). With a proximal venous tourniquet, IOP increased from 15.1 mmHg (SD 11.3 mmHg) to 44.9 mmHg (SD 24 mmHg), p < 0.0001, n = 9. Filling and emptying curves during perfusion and with using a tourniquet were similar, indicating that the model behaves in an elastic hydrodynamic manner. In fresh feet IOP peaked after about 1 min irrespective of perfusion pressure, possibly due to auto regulation. Older feet showed a continuously rising IOP and became oedematous. There was no significant difference in IOP between fresh and old feet perfused with serum at 150 cms pressure for 1 min. CONCLUSION: Though basal intraosseous pressure varies, IOP behaves predictably. IOP measurements reflect the perfusion microclimate at the individual needle tip. This 3Rs compliant model will be used for further exploration of subchondral perfusion physiology with loading. Springer Berlin Heidelberg 2019-08-30 /pmc/articles/PMC6717224/ /pubmed/31471704 http://dx.doi.org/10.1186/s40634-019-0207-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Beverly, Michael
Murray, David
An in vitro model to explore subchondral perfusion and intraosseous pressure
title An in vitro model to explore subchondral perfusion and intraosseous pressure
title_full An in vitro model to explore subchondral perfusion and intraosseous pressure
title_fullStr An in vitro model to explore subchondral perfusion and intraosseous pressure
title_full_unstemmed An in vitro model to explore subchondral perfusion and intraosseous pressure
title_short An in vitro model to explore subchondral perfusion and intraosseous pressure
title_sort in vitro model to explore subchondral perfusion and intraosseous pressure
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717224/
https://www.ncbi.nlm.nih.gov/pubmed/31471704
http://dx.doi.org/10.1186/s40634-019-0207-3
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