Ex vivo effects of corticosteroids on equine deep digital flexor and navicular fibrocartilage explant cell viability.
Abstract: To investigate the effects of triamcinolone acetonide (TA) and methylprednisolone acetate (MPA) on the viability of resident cells within the fibrocartilage on the dorsal surface of the deep digital flexor tendon (FC-DDFT) and fibrocartilage on the flexor surface of the navicular bone (FC-NB) of horses. Methods: 12 to 14 explants of FC-DDFT and of FC-NB from grossly normal forelimbs of 5 cadavers of horses aged 9 to 15 years without evidence of musculoskeletal disease. Methods: Explants were incubated with culture medium (control) or TA-supplemented (0.6 or 6 mg/mL) or MPA-supplemented (0.5 or 5 mg/mL) medium for 6 or 24 hours. Explant metabolic activity and percentage of dead cells were assessed with a resazurin-based assay and live-dead cell staining, respectively, at each time point. Drug effects were assessed relative to findings for the respective control group. Results: Application of TA (at both concentrations) did not significantly change the cell viability of FC-DDFT explants. For FC-NB explants, TA at 6 mg/mL significantly reduced the metabolic activity and increased the percentage of dead cells at both time points. With either MPA concentration, FC-DDFT and FC-NB explants had reduced metabolic activity and an increased percentage of dead cells at 24 hours, whereas only MPA at 5 mg/mL was cytotoxic at the 6-hour time point. Conclusions: In ex vivo explants, TA was less cytotoxic to equine FC-DDFT and FC-NB cells, compared with MPA. Further work is warranted to characterize the drugs' transcriptional and translational effects as well as investigate their cytotoxicity at lower concentrations.
Publication Date: 2021-01-23 PubMed ID: 33480274DOI: 10.2460/ajvr.82.2.125Google Scholar: Lookup
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- Journal Article
Summary
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This study examines the impact of two types of corticosteroids, triamcinolone acetonide (TA) and methylprednisolone acetate (MPA), on the health of cells in the fibrocartilage within a horse’s deep digital flexor tendon and navicular bone. The research suggests that TA is less harmful to these cells than MPA, but also suggests further research is required to fully understand the effects of these drugs.
Methods
- The researchers used 12 to 14 explants of fibrocartilage from the deep digital flexor tendon (FC-DDFT) and the navicular bone (FC-NB) from the forelimbs of 5 horses aged 9 to 15 years. These horses didn’t show any evidence of musculoskeletal disease.
- The fibrocartilage explants were incubated in a control culture medium, or in a medium supplemented with either TA (0.6 or 6 mg/mL) or MPA (0.5 or 5 mg/mL) for 6 or 24 hours.
- At each time point, researchers assessed fibrocartilage explants for metabolic activity (using a resazurin-based assay) and for the percentage of dead cells (using live-dead cell staining).
- The effects of the drugs on the explants were assessed in comparison with the control group.
Findings
- For FC-DDFT explants, TA did not significantly affect cell viability at either concentration.
- However, for FC-NB explants, TA at a concentration of 6 mg/mL significantly reduced metabolic activity and increased the percentage of dead cells at both 6 and 24 hour time points.
- With MPA at either concentration, both FC-DDFT and FC-NB explants showed a decrease in metabolic activity and an increase in dead cells at the 24 hour time point. At the 6 hour time point, only a higher concentration of MPA (5 mg/mL) showed cytotoxic effects.
Conclusions
- Ex vivo (outside the living body) studies showed that TA was less harmful to the cells of equine FC-DDFT and FC-NB than MPA.
- The study suggests that further research is needed to understand how these drugs affect cellular transcription and translation. It is also suggested to investigate their cytotoxicity at lower concentrations.
Cite This Article
APA
Sullivan SN, Cole SL, Stewart MC, Brokken MT, Durgam S.
(2021).
Ex vivo effects of corticosteroids on equine deep digital flexor and navicular fibrocartilage explant cell viability.
Am J Vet Res, 82(2), 125-131.
https://doi.org/10.2460/ajvr.82.2.125 Publication
Researcher Affiliations
MeSH Terms
- Adrenal Cortex Hormones
- Animals
- Cell Survival
- Fibrocartilage
- Horse Diseases / drug therapy
- Horses
- Tarsal Bones
Citations
This article has been cited 2 times.- Maglio M, Fini M, Sartori M, Codispoti G, Borsari V, Dallari D, Ambretti S, Rocchi M, Tschon M. An Advanced Human Bone Tissue Culture Model for the Assessment of Implant Osteointegration In Vitro. Int J Mol Sci 2024 May 13;25(10).
- Quam VG, Belacic ZA, Long S, Rice HC, Dhar MS, Durgam S. Equine bone marrow MSC-derived extracellular vesicles mitigate the inflammatory effects of interleukin-1β on navicular tissues in vitro. Equine Vet J 2025 Jan;57(1):232-242.
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