Histologic comparison of the dura mater among species

Publication date

2020-04

Authors

Kinaci, Ahmet
Bergmann, Wilhelmina
Bleys, Ronald L A WISNI 0000000050357498
van der Zwan, AlbertISNI 0000000396044595
van Doormaal, Tristan P CORCID 0000-0002-6299-3859ISNI 0000000389942725

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Document Type

Article

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License

taverne

Abstract

The biocompatibility, biodegradation, feasibility, and efficacy of medical devices like dural sealants and substitutes are often evaluated in various animal models. However, none of these studies explain the rationale for choosing a particular species, and a systematic interspecies comparison of the dura is not available. We hypothesized that histologic characteristics of the dura would differ among species. We systematically investigated basic characteristics of the dura, including thickness, composition, and fibroblast orientation of the dura mater, in 34 samples representing 10 animal species and compared these features with human dura by using hematoxylin and eosin staining and light microscopy. Dura showed many similarities between species in terms of composition. In all species, dura consisted of at least one fibrovascular layer, which contained collagen, fibroblasts, and blood vessels, and a dural border cell layer beneath the fibrovascular layer. Differences between species included the number of fibrovascular layers, fibroblast orientation, and dural thickness. Human dura was the thickest (564 μm) followed by equine (313 μm), bovine (311 μm), and porcine (304 μm) dura. Given the results of this study and factors such as gross anatomy, feasibility, housing, and ethical considerations, we recommend the use of a porcine model for dural research, especially for in vivo studies.

Keywords

Taverne, General Biochemistry,Genetics and Molecular Biology, General Veterinary

Citation

Kinaci, A, Bergmann, W, Bleys, R L A W, van der Zwan, A & van Doormaal, T P C 2020, 'Histologic comparison of the dura mater among species', Comparative Medicine, vol. 70, no. 2, pp. 170-175. https://doi.org/10.30802/AALAS-CM-19-000022